The authors would also like to thank all participants who donated samples for this work. This work was funded by the Office of Justice Program, National Institute of Justice, Department of Justice under award number 2010-DN-BX-K139. The funding agencies had no involvement in the study design, in collection, analysis and interpretation of data, or in the writing of the report. Points of view in this document are those of the authors and do not necessarily represent the official positions of the U.S. Department of Justice.

NOTE: Body fluids were collected from volunteers using procedures approved by the University of Central Florida&#8217;s Institutional Review Board. Informed written consent was obtained from each donor.
1. Collection of Bioparticles from Touched Objects and Surfaces
<ol>
	<li>Cut the gel-film to the desired size. Ensure that it is the appropriate size for the glass microscope slide being used as the solid support. For example, for a 3&#8221; x 1&#8221; glass slide, use a gel-film size of 2&#8221; x 0.75&#8221;. 
	NOTE: The length and width of the material can be reduced, if desired, but should not exceed this size.</li>
	<li>Remove the white backing from the gel-film and attach the gel-film to the microscope slide (Figure 1A). Press down firmly to ensure a complete attachment. 
	NOTE: There is a clear top protective layer that should not be removed to allow pressure to be applied along the piece of gel-film without contaminating the gel-film surface. Prepared gel-film slides (with protective layer attached) can be stored at room temperature until needed.</li>
	<li>Remove the clear top protective film from the gel-film using sterile tweezers when ready to use (Figure 1B) the gel-film sample. Place the gel-film surface in direct contact with the desired touched object or surface (Figure 2). Apply a small amount of pressure to ensure efficient transfer of bio-particles to the gel-film. 
	NOTE: If too much pressure is applied, the glass slide could break. 
	NOTE: Multiple samplings from the same object or surface can be collected onto the same piece of gel-film.</li>
	<li>Confirm the transfer of bio-particles onto the gel-film (Figure 3) by placing the slide on a stereomicroscope (trans- or epi-illumination can be used). Use magnification of ~20X for best viewing larger areas of the gel-film, and magnification of ~200X for best viewing individual bio-particles.</li>
	<li>Store the gel-film sample slide at room temperature in a covered slide box or use immediately for staining and/or bio-particle collection.</li>
</ol>
2. Optional Staining of Bioparticles to Aid in Visualization
<ol>
	<li>Place the gel-film sample slide prepared in Step 1 onto a slide-staining rack over a sink.</li>
	<li>Using a disposable transfer pipet, cover the entire gel-film surface with trypan blue stain (Figure 4A). Incubate at room temperature for 1-2 min.</li>
	<li>Remove excess stain by tilting the slide to allow the stain to drain off into the sink (Figure 4B). 
	NOTE: The slide can be rinsed by gentle flooding with sterile water using a disposable transfer pipet if needed (Figure 4C).</li>
	<li>Allow the slide to air dry before proceeding to isolation of bio-particles. View the slide using a stereomicroscope (~20X for overall viewing and ~200-300X to view individual bioparticles) to ensure proper staining (Figure 4D-E). 
	NOTE: The slide can be stored at room temperature in a covered slide box.</li>
</ol>
3. Isolation of Bioparticles of Interest for Analysis
<ol>
	<li>Place the appropriate number of 0.2 ml PCR tubes in a rack and label the tubes appropriately.</li>
	<li>Prepare the STR amplification mix (see Materials List) in a designated PCR amplification hood or biosafety cabinet. Vortex the master mix well and briefly centrifuge in a mini-centrifuge.
	<ol>
		<li>The volume of amplification mix needed per sample is 3.5 &#181;l; prepare an appropriate volume of master mix for the desired number of samples.</li>
	</ol>
	</li>
	<li>Pipet 3.5 &#181;l of amplification mix into each 0.2 ml tube. Cap each tube loosely.</li>
	<li>Place a piece of double stick tape onto a clean glass microscope slide or directly onto a glass block. 
	NOTE: This will be used to hold the 0.2 ml tube in place during sample collection.</li>
	<li>Place a piece of double stick tape onto a clean glass microscope slide. Place a piece of water-soluble wave solder tape on top of the double stick tape. 
	NOTE: This slide can be stored in a desiccator for future use.</li>
	<li>Place the first 0.2 ml tube onto the double stick tape slide or block prepared in step 3.4. Set this tube aside until the sample is collected.</li>
	<li>Place the water-soluble wave solder tape slide under the microscope (low magnification). Using the tip of a tungsten needle, gently scrape the surface of the tape in order to collect a small amount (or &#8220;ball&#8221;) of adhesive at the end of the needle (Figure 5A). 
	NOTE: The size of the ball can be made small or large depending on the number of bioparticles that will be collected.</li>
	<li>Carefully remove the tungsten needle with adhesive from under the microscope without disturbing the tip of the needle. The needle can be place in a rack if desired during sample placement.</li>
	<li>Place the prepared gel-film sample (from Steps 1 and 2) on the microscope stage. Adjust the focus and magnification until the bioparticles can be easily viewed. Identify the bio-particles that will be collected. 
	NOTE: A glass block can be used to support the slide if needed.</li>
	<li>Retrieve the tungsten needle with adhesive ball, and place the needle over the gel-film surface where the bio-particles of interest are located. Press the tip of the needle (with adhesive) down so that it is in contact with the bio-particle (Figure 5B). Lift the needle up to ensure that the bio-particle has been collected. Repeat this process until the desired number of bio-particles has been collected.</li>
	<li>Place the prepared 0.2 ml PCR tube on the microscope stage. Adjust the magnification so that the bottom of the tube containing the amplification mix is in focus.</li>
	<li>Carefully insert the tungsten needle into the 0.2 ml PCR tube until the tip of the needle is in the amplification mix. 
	NOTE: This is best performed while viewing through the microscope.</li>
	<li>Hold the needle in the amplification mix until the adhesive dissolves and the bioparticles are released into solution (Figure 5C). Remove the needle, place the 0.2 ml upright and loosely cap the tube.</li>
	<li>Repeat the collection procedure for additional samples. Clean the tungsten needle with pre-moistened alcohol (isopropanol) wipes in between samples.</li>
</ol>
4. Combined Microvolume Nucleic Acid Isolation (Direct Lysis) and Autosomal Short Tandem Repeat (STR) Profiling
<ol>
	<li>Prepare the lysis buffer (see Materials) in a designated PCR amplification hood or biosafety cabinet. Add 1.5 &#181;l of the lysis buffer to each tube for a 5 &#181;l total reaction volume. Close tube lids tightly. 
	NOTE: The 0.2 ml tubes already contain 3.5 &#181;l of the amplification mix and the collection bio-particles from Step 3.</li>
	<li>Place samples in the thermal cycler and amplify the samples using the following cycling conditions: 75 &#176;C for 15 min; 95 &#176;C for 11 min; 34 cycles of 94 &#176;C for 20 sec and 59 &#176;C for 3 min; 60 &#176;C for 10 min; and 4 &#176;C hold.
	<ol>
		<li>Store amplification products at 4 &#176;C for short term storage.</li>
	</ol>
	</li>
</ol>
5. Product Detection &#8211; Capillary Electrophoresis (CE)
<ol>
	<li>In a 96 well plate, add 10 &#181;l of CE running mix (9.7 &#181;l deionized formamide and 0.3 &#181;l size standard, see Materials). Add 1 &#181;l of amplified product or allelic ladder to each well. 
	CAUTION: Formamide is a potential mutagen and should be handled in a chemical hood while wearing suitable personal protective equipment.</li>
	<li>Use electrophoretic conditions specified by the manufacturer in the amplification kit manual or internally validated conditions.</li>
	<li>Analyze raw data with STR analysis software.</li>
</ol>

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The authors declare that they have no competing financial interests.

Here we have described methods for the collection and enhanced genetic analysis of bioparticles recovered from touch DNA evidence. The developed approach involves the following: 1) collection of biological material (i.e., bioparticles) via gel-film from touched objects and surfaces, worn clothing items or direct human skin, 2) microscopic examination of the recovered biological material to ensure collection of potential human biological material, and 3) micromanipulation of single or few bioparticles using a water soluble adhesive, and 4) autosomal DNA-STR profiling of the collected bioparticles using a microvolume (5 &#181;l) one-step lysis/amplification reaction. The use of a one-step closed tube reaction reduces the potential for contamination and sample loss from additional sample manipulations or transfer to other reaction tubes. The enhanced one-step microvolume (5 &#181;l) lysis/STR amplification reactions permits the recovery of full or probative STR profiles of the donor of single or few bioparticles. This approach was developed to obtain single source STR profiles from single- and multi-source touch DNA evidence (e.g., worn clothing items and other household items, touched/handled objects and surfaces, skin/skin mixtures). It has successfully been used for the detection of the male donor in simulated physical assault mixture samples.
This approach could be further evaluated in additional body fluid/tissue mixture scenarios such as a victim scratching his/her assailant, in which only a few bioparticles from the assailant would be present amongst an overwhelming amount of biological material from the victim. Additionally, since this approach developed in the current study permits analysis at the single bioparticle level, it could be used to gain a better understanding of the nature and extent of secondary transfer14-19, in which an intermediary transfers a DNA profile on a surface, object or person to another surface object or person20. A blind-swabbing approach to the analysis of secondary transfer may fail to identify trace amounts of material from the secondary donor. The approach developed here permits the analysis of single or few bioparticles and therefore the results are not confounded by the presence of an overwhelming amount of biological material from the primary donor. The methodologies developed in this work may also have implications for the analysis of trace biological material in sexual assault cases such as those involving digital penetration of the vagina where positive identification of trace amounts of skin cells from the perpetrator could be crucial to establish that sexual contact occurred.
While the collection of bioparticles from gel-film sample does not involve difficult and complex manipulations, there are critical steps in this procedure that need to be performed with great care to ensure the successful transfer of bioparticles to the downstream reaction vessel. The collection of bioparticles with the water soluble adhesive must be viewed microscopically (i.e., stereomicroscope at high magnification (~200-300X) to ensure that only the bioparticles of interest are collected. Depending on the size of the adhesive &#8220;ball&#8221; used, there is the potential to collect additional surrounding material which may include both biological and non-biological material (e.g., fibers, other debris). The collection of unintended additional bioparticles may result in the recovery of admixed DNA profiles. The collection of non-biological material may introduce inhibitors into the micro-volume lysis/STR reactions. If multiple bioparticles are collected with the same adhesive &#8220;ball&#8221;, there is a potential for previously collected bioparticles to become unattached from the adhesive. This is not frequently observed, but can occur when larger numbers of bioparticles are collected (e.g., over 50) with a single adhesive &#8220;ball&#8221;. If a large number of bioparticles are targeted, it is recommended that multiple collections of fewer bioparticles are made but all transferred into the same 0.2 ml tube. Once bioparticles have been collected, care must be taken during the removal of the gel-film slide from the microscope stage and the placement of the 0.2 ml tube so that the tip of the needle is not disturbed. During placement of the tip of the needle into the amplification mix at the bottom of the 0.2 ml tube, the tip of the needle should not make contact with the sides of the tube in order to avoid loss of material on the sides of the tube. While the solubilization of the adhesive is typically rapid (~30 sec or less depending on the size of the adhesive &#8220;ball&#8221;) and can monitored during microscopic examination, the tip of the needle should be slowly removed from the amplification mix to ensure that complete solubilization of the adhesive has been achieved. If the adhesive has not completely dissolved, the needle can be returned to the liquid to allow complete dissolution.
The protocols described here have been optimized for use with bioparticles and human cells from forensic biological evidence. The lysis buffer selected is compatible with the selected DNA-STR amplification kit. While there may be suitable alternative lysis buffers, their efficiency in terms of cell lysis and compatibility with downstream analysis must be verified by the user. Additionally, the STR amplification kit and amplification cycle number described in this protocol have been optimized for use with single or few bioparticles. A next generation STR amplification kit with reported increased robustness and sensitivity was selected and has been demonstrated to result in the recovery of high quality STR profiles from single or few bioparticles. While numerous other STR kits, with varying recommended amplification cycle numbers, are available, they may not possess suitable sensitivity and therefore would need to be properly evaluated before use in these protocols.
Despite the successful use of the described methods for the recovery STR profiles from single or few bioparticles, the success rate of profile recovery will not be 100%. Therefore, for some samples a limited partial DNA profile or no profile may be observed. This cannot be avoided due to the inability to conclusively visually identify most bioparticles as cellular material, the potential degraded state of the nuclear material in the collected bioparticles or loss of sample material from the adhesive before transfer into the reaction vessel. Therefore, the analysis of a single bioparticle sample for each touch DNA item is not recommended. We frequently collect 20 sample sets from an individual gel-film sample and will collect additional sample sets as needed if a suitable STR profile is not obtained. The only limitation for collections is the amount of biological material present on the gel-film sample (and likely the cost of analysis, although the microvolume reactions provide the opportunity to collect additional samples for a similar or lower cost as a single standard reaction volume (e.g., 25 &#181;l).
The developed DNA profiling methods describe here provide a molecular based approach to the characterization, analysis and interpretation of trace biological material recovered from touch DNA samples. However, there is additional genetic information that can be obtained from the recovered bioparticles in addition to determination of the donor (i.e., STR profile) of the donor of the biological material. The tissue or body fluid source of origin (e.g., skin versus saliva) may provide crucial contextual information to a criminal investigation. Without such a determination, the ambiguity of the tissue source of origin can be exploited as alternative circumstances of the crime (e.g., how the body fluid may have been deposited) could be suggested. The bioparticle collection and isolation protocols described here could be used to collect bioparticles or other cells (e.g., buccal, vaginal) for use in a tissue source identification (mRNA profiling21-30) strategy that involves micro-volume reverse transcription (RT) and amplification reactions. With further optimization it may also be possible to develop a DNA/RNA co-isolation strategy to permit cell type identification (RNA) and STR profiling from the same sample, including bioparticles from touch DNA evidence.

Touch DNA is a form of trace biological evidence which is the direct transfer of cellular material (e.g., shed skin cells) from an individual to an object or another individual during physical contact1. The ability to obtain DNA profiles from a variety of touched objects (documents, bedding, shoes, firearms, drinking containers, pens, briefcase handles) has been reported in the literature2-9.
A critical factor in the analysis of touch DNA evidence is the successful recovery of the trace biological material present. Touch DNA evidence is typically collected by swabbing the suspected area with a sterile cotton swab (referred to as &#8220;blind-swabbing&#8221;). Using this approach, the nature of the collected biological material is not known and sampling of a generalized area is performed. The presence of surface grooves or crevices may impede the successful recovery of the often already small amount of biological material present. Additionally, a &#8216;blind-swabbing&#8217; approach will necessarily co-sample cellular material from the different individuals whose cells are present on the item, even if the individuals&#8217; cells are located in spatially distinct locations on the item. The recovery of admixed DNA profiles, which are often challenging to resolve particularly with low template DNA samples, is frequently observed8,10,11 and in many instances will be a consequential artifact of the swabbing process itself. If only a small amount of material was present from one of the donors, standard extraction and analysis techniques may fail to recover a profile from the minor contributor. Additionally, the type of swab or whether it was used dry or wet (pre-moistened with sterile water) may influence the amount of biological material that is collected due to differences in absorptivity and adsorptivity and the efficiency of release of the biological material12. Standard extraction methods may result in additional sample loss due to required physical manipulation of the sample or sample transfer steps.
As described above, simple swabbing techniques for the recovery of biological material may result in the loss of trace amounts of biological sample as well as an increased occurrence of admixed profiles due to a failure to separate individual biological components. Therefore, we sought to develop more selective and efficient recovery strategies for collection of cellular microparticles present on touched objects. The developed strategy for the analysis of biological material from touch DNA evidence (referred to here as &#8220;bioparticles&#8221; due to the fact that a nucleus is not always visible since a majority of the cells found in the outer epidermal layer of skin are dead or dying keratinocytes13) involves the following: 1) collection of biological material (i.e., bioparticles) via gel-film from touched objects and surfaces, worn clothing items or direct human skin, 2) microscopic examination of the recovered biological material to ensure collection of potential human biological material, and 3) micromanipulation of single or few bio-particles using a water soluble adhesive, and 4) autosomal DNA-STR profiling of the collected bio-particles using a microvolume (5 &#181;l) one-step lysis/amplification reaction.
This procedure offers numerous advantages over traditionally used analysis methods. Recovery of bioparticles using the gel-film permits a microscopic examination of the biological material present in the sample prior to analysis. While a majority of the bioparticles recovered from touch DNA evidence may not be nucleated cells making it more difficult to determine which or how many bio-particles should be selected, the microscopic examination of these samples prior to analysis provides to opportunity to search for nucleated cells thus maximizing the probability of DNA profile recovery. The collection of bioparticles using water soluble adhesive-assisted micromanipulation permits the direct transfer of targeted bioparticles into reaction tubes. This procedure is visualized under the microscope to ensure successful transfer of the biological material. The reduced or microvolume reaction increases sensitivity while reducing the cost of analysis per sample. This permits the analysis of increased numbers of samples from an individual piece of evidence. Due to the range in the genetic state of bio-particles in touch DNA evidence, multiple samplings from individual items are recommended.
Here, we demonstrate the successful use of the developed protocols to obtain highly probative genetic profiles of the donors of biological material in touch DNA evidence. The developed bioparticle collection and DNA profiling methods provide a comprehensive &#8216;smart&#8217; (i.e., specific, measurable, attainable, realistic and timely) molecular based approach to the characterization, analysis and interpretation of trace biological material. While originally developed for application to forensic analysis of touch DNA evidence, the strategies developed here can be applied to other sources of biological material and offer an opportunity to obtain individual identifying information at the single cell level.

<table border="0" cellpadding="0" cellspacing="0" width="998">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Name of Material/ Equipment</td>
			<td style="width:147px;">Company</td>
			<td style="width:139px;">Catalog Number</td>
			<td style="width:320px;">Comments/Description</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">SealRite 1.5 mL natural microcentrifuge tubes, sterile</td>
			<td style="width:147px;">USA Scientific</td>
			<td style="width:139px;">1615-5510</td>
			<td style="width:320px;">numerous altnerative suppliers are available, but tubes should be sterile</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">0.2 mL PCR tubes with flat cap, natural</td>
			<td style="width:147px;">Phenix Research</td>
			<td style="width:139px;">MPX-200F</td>
			<td style="width:320px;">or equivalent</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">Kimwipes</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:139px;">06-666 and/or 06-666-11C</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="44">
			<td height="44" style="height:44px;width:395px;">Alcohol prep pads</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:139px;">06-669-62</td>
			<td style="width:320px;">alternative is 06-665-24 (Fisher Sci); canister of larger alcohol wipes rather than individual pads</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Sterile water</td>
			<td style="width:147px;"></td>
			<td style="width:139px;"></td>
			<td style="width:320px;">18.2 mega-ohm, autoclaved</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Glass microscope slides, frosted, 3&#34; x 1&#34;: 1mm</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:139px;">12-544-3</td>
			<td style="width:320px;">alternative brands or sizes are acceptable</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Disposable transfer pipet</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:139px;">13-711-9D</td>
			<td style="width:320px;">alternatives are acceptable</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Trypan blue solution</td>
			<td style="width:147px;">Sigma</td>
			<td style="width:139px;">T8154</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Pipets: 0.2-2, 2-20, 10-100, 100-1,1000 mL</td>
			<td style="width:147px;">various</td>
			<td style="width:139px;"></td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Sterile, aerosol-resistant pipet tips</td>
			<td style="width:147px;">various</td>
			<td style="width:139px;"></td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Mini-centrifuge</td>
			<td style="width:147px;">various</td>
			<td style="width:139px;"></td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">Stereomicroscope</td>
			<td style="width:147px;">Leica</td>
			<td style="width:139px;">M205C</td>
			<td style="width:320px;">others are suitable, but must be capable of magifications up to 350X</td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:395px;">GeneAmp PCR system 9700 thermal cycle (silver or gold block)</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">N8050200 or 4314878</td>
			<td style="width:320px;">other models and manufacturers can be used, but performance with the STR amplification kit must be verified</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">3130 Genetic Analyzer</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">3130-01</td>
			<td style="width:320px;">Alternatives: 310 or 3500 Genetic Aanlyzers (Life Technologies)</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">GeneMapper software</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">various</td>
			<td style="width:320px;">Various versions of the software are available and can be used</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:395px;">WF Gel-Film , x8 retention level</td>
			<td style="width:147px;">Gel-Pak</td>
			<td style="width:139px;">WF-40-x8-A</td>
			<td style="width:320px;">4&#34; x 4&#34; wafer film; can be ordered in other size specifications</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Double sided tape</td>
			<td style="width:147px;">various</td>
			<td style="width:139px;"></td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:395px;">Glass block, 3&#34; x 1.5&#34; x 3/8&#34;</td>
			<td style="width:147px;">McCrone Microscopes and Accessories</td>
			<td style="width:139px;">370-2</td>
			<td style="width:320px;">or equivalent</td>
		</tr>
		<tr height="63">
			<td height="63" style="height:63px;width:395px;">Tungsten needle with holder</td>
			<td style="width:147px;">McCrone Microscopes and Accessories</td>
			<td style="width:139px;">106</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">3M&#160; water soluble wave solder tape, 5414 transparent</td>
			<td style="width:147px;">Allied Electronics</td>
			<td style="width:139px;">70113977</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="147">
			<td height="147" style="height:147px;width:395px;">Lysis buffer (forensicGEM Saliva, Zygem)</td>
			<td style="width:147px;">VWR</td>
			<td style="width:139px;">95043-992</td>
			<td style="width:320px;">Lysis buffer is prepared in 10 ml portions (prepare additional master mix portions as needed to accommodate the desired number of samples). 1.5 ml is used for each sample. To prepare 10 ml of lysis buffer (sufficient for ~6 samples): 6.9 mL sterile water, 2.1 mL 10x buffer - blue, 1 mL forensicGEM.&#160;</td>
		</tr>
		<tr height="210">
			<td height="210" style="height:210px;width:395px;">STR Amplification kit, AmpFlSTR Identifiler Plus PCR amplification kit</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">4427368</td>
			<td style="width:320px;">Alternative STR amplification kits can be used, but performance would have to be verified by user. The amplification mix is prepared as follows (volumes per sample): 2.2 ml PCR reaction mix, 1.1 ml Primer set, 0.2 ml (1U) AmpliTaq Gold DNA polymerase. A master mix sufficient for the desired number of samples should be prepared. 3.5 ml of the prepared mix is added to the 0.2 mL tube for bio-particle collection.&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">AmpliTaq Gold DNA polymerase</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">N808-0245</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">HiDi formamide</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">4311320</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">GeneScan 500 LIZ size standard</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">4322682</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">96 well optical reaction plates</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">N8010560</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Plate septa, 96 well</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">4315933</td>
			<td style="width:320px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:395px;">Performance-optimized polymer, POP-7</td>
			<td style="width:147px;">Life Technologies</td>
			<td style="width:139px;">4363785</td>
			<td style="width:320px;">Alternatives such as POP-4 are acceptable</td>
		</tr>
	</tbody>
</table>

enhanced genetic analysis of single human bioparticles recovered by simplified micromanipulation from forensic &#8216;touch dna&#8217; evidence

DNA profiles can be obtained from &#8216;touch DNA&#8217; evidence, which comprises microscopic traces of human biological material. Current methods for the recovery of trace DNA employ cotton swabs or adhesive tape to sample an area of interest. However, such a &#8216;blind-swabbing&#8217; approach will co-sample cellular material from the different individuals, even if the individuals&#8217; cells are located in geographically distinct locations on the item. Thus, some of the DNA mixtures encountered in touch DNA samples are artificially created by the swabbing itself. In some instances, a victim&#8217;s DNA may be found in significant excess thus masking any potential perpetrator&#8217;s DNA.
In order to circumvent the challenges with standard recovery and analysis methods, we have developed a lower cost, &#8216;smart analysis&#8217; method that results in enhanced genetic analysis of touch DNA evidence. We describe an optimized and efficient micromanipulation recovery strategy for the collection of bio-particles present in touch DNA samples, as well as an enhanced amplification strategy involving a one-step 5 &#181;l microvolume lysis/STR amplification to permit the recovery of STR profiles from the bio-particle donor(s). The use of individual or few (i.e., &#8220;clumps&#8221;) bioparticles results in the ability to obtain single source profiles. These procedures represent alternative enhanced techniques for the isolation and analysis of single bioparticles from forensic touch DNA evidence. While not necessary in every forensic investigation, the method could be highly beneficial for the recovery of a single source perpetrator DNA profile in cases involving physical assault (e.g., strangulation) that may not be possible using standard analysis techniques. Additionally, the strategies developed here offer an opportunity to obtain genetic information at the single cell level from a variety of other non-forensic trace biological material.

Representative images of individual and clumped bioparticles that were recovered from a shirt collar (100% polyester) worn by a male donor are shown in Figure 6 (individual bioparticles) and Figure 7 (clumped bioparticles). The bioparticles were recovered from the shirt collar using the protocol described here: transfer of bioparticles from the shirt collar to gel-film through direct contact, staining of the recovered bioparticles with trypan blue, collection of bioparticle samples using a tungsten needle and water soluble adhesive and STR analysis using the 5 &#181;l micro-volume lysis/STR amplification. Figures 6 and 7 represent a typical sampling of bioparticles that would be analyzed from an individual touch DNA item (20 single/individual bioparticles and 20 clumped bioparticles). The bioparticle(s) collected in each image are labeled with length and width measurements (in microns). The percentage of STR alleles recovered from each of the collected bioparticle(s) is provided on each individual image to demonstrate the variable degrees of success that can be expected to be obtained from bioparticles with this type of evidence. The bioparticles recovered from touch DNA samples are largely dead or dying keratinocytes and therefore a probative STR profile is not obtained from each bioparticle collected, as can be seen in Figures 6 and 7. For this shirt collar sample, STR profiles were obtained from 14/20 (70%) of the individual bioparticles and 15/20 (75%) clumped bioparticles. However, each of the recovered profiles ranges in probative value: 3-97% allele recovery for individual bioparticles profiles and 3-100% allele recovery for the clumped bioparticle profiles. Due to the variability in success rates, the collection of numerous bioparticles from each touch DNA item is recommended. This ensures a better chance of obtaining a highly probative STR profile.
The STR profile obtained from one of the individual bioparticle samples from the shirt collar is shown in Figure 8 (the bioparticle from which the profile originated is shown to the left). Almost a full STR profile (28 out of 30 alleles, one locus drop out, accuracy of the obtained profile verified by comparison to a reference profile) was obtained from this individual bioparticle. The obtained profile is of high quality with reasonably balanced inter-locus peak heights and no allelic drop out. Allelic drop out and unbalanced peak height artifacts are both frequently observed with low template DNA samples. The STR profile obtained from one of the clumped bioparticle samples from the shirt collar is shown in Figure 9. A full STR profile (30/30 alleles, accuracy of the obtained profile verified by comparison to a reference profile) was obtained. As mentioned previously, an STR profile is not recovered from every bioparticle collected. An example of unsuccessful DNA profiling of a single bioparticle (3% allele recovery, 1/30 alleles) is shown in Figure 10 (individual bioparticle). While this individual bioparticle was not successful, highly probative STR profiles of the donor of the bioparticles in this sample were obtained from other bioparticles recovered from the same sample. This illustrates the need to perform multiple single cell/clump samplings from the same object.
The developed &#8220;smart&#8221; analysis methods described here for touch DNA evidence have been used successfully to recover probative single source profiles from single and &#8220;clumped&#8221; bioparticles from various touched objects and clothing items (e.g., chair armrests, car steering wheels, cell phones, coffee cups, cigarettes, pens, shirts, shorts, and sweaters). However, importantly, this approach has also been used for the detection and profiling of male donor DNA (single source) in simulated physical contact/assault mixture samples (e.g., perpetrator grabbing a victim&#8217;s wrist, neck or clothing, or contact with victim&#8217;s bedding as in sexual assaults).
<img alt="Figure 1" src="/files/ftp_upload/52612/52612fig1.jpg" /> 
Figure 1: Preparation of gel-film slides for bioparticle collection. (A) The white back protective cover is removed using sterile tweezers from the piece of gel-film to expose the adhesive backing. The gel-film is then adhered to a glass microscope slide with firm pressure. (B) When the gel-film sample is ready to be used for bioparticle collection, the top clear protective film is removed using sterile tweezers.
<img alt="Figure 2" src="/files/ftp_upload/52612/52612fig2.jpg" /> 
Figure 2: Bioparticle collection using gel-film from various substrates. The gel-film slides can be used to collect bioparticles from a variety of surfaces. The gel-film is placed in direct contact with the object or surface of interest. Gentle pressure is applied in order to transfer bioparticles onto the gel-film surface. Collection of bioparticles from (A) worn clothing items (coat collar), (B) touched objects (travel coffee cup), and (C) direct human skin (male wrist) are shown.
<img alt="Figure 3" src="/files/ftp_upload/52612/52612fig3.jpg" /> 
Figure 3: Bioparticles on a worn clothing item (inside pant leg). Bioparticles are transferred to gel-film through direct contact with the object surface. Bioparticles can be found as &#8220;clumps&#8221; or individual/single bioparticles (indicated with red arrows).
<img alt="Figure 4" src="/files/ftp_upload/52612/52612fig4.jpg" /> 
Figure 4: Optional staining of bioparticles on gel-film slides. For better visualization of bioparticles, gel-film samples can be stained with trypan blue stain. The entire surface of gel-film is covered by trypan blue (A). After 1-2 min of staining, the slide is gently tilted to allow excess stain to run off the slide (B). Gentle flooding with sterile water (C) can be used to remove excess stain. After the slide is air dried, the slide can be viewed under the microscope to ensure proper staining (D, E). Note: Not all bioparticles will appear stained (i.e., blue in color). <a href="https://www.jove.com/files/ftp_upload/52612/52612fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" src="/files/ftp_upload/52612/52612fig5.jpg" /> 
Figure 5: Bioparticle collection and analysis. (A) A small amount (or &#8220;ball&#8221;) of water&#8211;soluble wave solder tape (&#8220;adhesive&#8221;) is collected on to the tip of a tungsten needle by gentle scraping. (B) The adhesive is then touched to the gel-film surface in order to collect the bioparticles of interest. Individual or multiple bioparticles can be collected with a single adhesive ball. (C) Once the desired bioparticles have been collected, the tip of the needle is placed into amplification mix in a 0.2 ml PCR tube. The needle is held in the liquid until it dissolves and the release of bioparticles into solution is observed. All steps in the collection process are performed and viewed under the microscope to ensure successful bioparticle collection and transfer. <a href="https://www.jove.com/files/ftp_upload/52612/52612fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" src="/files/ftp_upload/52612/52612fig6.jpg" /> 
Figure 6: Individual bioparticles in a shirt collar sample. Bioparticles were recovered using gel-film from the inside of a shirt collar worn by a male donor. The bioparticles were stained using trypan blue and images of twenty different individual bioparticles identified in the sample are shown. In each image, the bioparticle that was collected is circled (red circles indicating bioparticles in which a profile was recovered; black circles indicating bioparticles in which a profile was not recovered). The percent allele recovery (number of observed alleles out of a possible 30) is shown above the image of bioparticle from which a profile was recovered. <a href="https://www.jove.com/files/ftp_upload/52612/52612fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 7" src="/files/ftp_upload/52612/52612fig7.jpg" /> 
Figure 7: Clumped bioparticles in a shirt collar sample. Bioparticles were recovered using gel-film from the inside of a shirt collar worn by a male donor. The bioparticles were stained using trypan blue and images of twenty different clumped bioparticles identified in the sample are shown. In each image, the bioparticle that was collected is circled (red circles indicating bioparticles in which a profile was recovered; black circles indicating bioparticles in which a profile was not recovered. The percent allele recovery (number of observed alleles out of a possible 30) is shown for each bioparticle from which a profile was recovered. <a href="https://www.jove.com/files/ftp_upload/52612/52612fig7large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 8" src="/files/ftp_upload/52612/52612fig8.jpg" /> 
Figure 8: Autosomal STR profile obtained from a single bioparticle from a male shirt collar. An autosomal STR profile was obtained from a single bioparticle (shown on left) using the 5 &#181;l direct lysis/amplification reaction. The accuracy of this profile was determined by comparison to a donor reference sample. Fifteen autosomal STR loci and amelogenin (sex determination) are co-amplified in a single reaction and separated by capillary electrophoresis. The results are displayed here as an electropherogram. Allele numbers are designation below each peak at each locus. The x-axis represents fragment size (base pairs, bp) and y-axis represents signal intensity (RFU relative fluorescence units; provided under each corresponding allele number). <a href="https://www.jove.com/files/ftp_upload/52612/52612fig8highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 9" src="/files/ftp_upload/52612/52612fig9.jpg" /> 
Figure 9: Autosomal STR profile obtained from a clumped bioparticle from a male shirt collar. An autosomal STR profile was obtained from a clumped bioparticle (shown on left) using the 5 &#181;l direct lysis/amplification reaction. The accuracy of this profile was determined by comparison to a donor reference sample. Fifteen autosomal STR loci and amelogenin (sex determination) are co-amplified in a single reaction and separated by capillary electrophoresis. The results are displayed here as an electropherogram. Allele numbers are designation below each peak at each locus. The x-axis represents fragment size (base pairs, bp) and y-axis represents signal intensity (RFU relative fluorescence units; provided under each corresponding allele number). <a href="https://www.jove.com/files/ftp_upload/52612/52612fig9highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 10" src="/files/ftp_upload/52612/52612fig10.jpg" /> 
Figure 10: Example of a failure to obtain an autosomal STR profile obtained from a collected bioparticle. The individual bioparticle shown on left was collected from a shirt collar gel-film sample. As can be seen from the resulting STR profile (shown on right), only one allele (out of 30 possible) was obtained. Allele numbers are designation below each peak at each locus. The x-axis represents fragment size (base pairs, bp) and y-axis represents signal intensity (RFU relative fluorescence units; provided under each corresponding allele number). <a href="https://www.jove.com/files/ftp_upload/52612/52612fig10highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Enhanced Genetic Analysis of Single Human Bioparticles Recovered by Simplified Micromanipulation from Forensic â€˜Touch DNAâ€™ Evidence at JoVE.com

Enhanced Genetic Analysis of Single Human Bioparticles Recovered by Simplified Micromanipulation from Forensic &amp;#8216;Touch DNA&amp;#8217; Evidence

Here we describe an optimized and efficient removal strategy for the collection of bio-particles present in &#8216;touch DNA&#8217; samples, together with an enhanced amplification protocol involving a one-step 5 &#181;l micro-volume lysis/STR amplification, to permit the recovery of short tandem repeat (STR) profiles of the bio-particle donor(s).

Enhanced Genetic Analysis of Single Human Bioparticles Recovered by Simplified Micromanipulation from Forensic &#8216;Touch DNA&#8217; Evidence

DNA profiles can be obtained from &#8216;touch DNA&#8217; evidence, which comprises microscopic traces of human biological material. Current methods for ...

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JoVE Journal

Biology

15.6K Görüntüleme.  University of Central Florida.  Burada mevcut olan biyo-parçacıkların toplanması için, optimize edilmiş ve etkin bir temizleme stratejisi tarif tek-aşamalı bir 5 ul mikro hacim liziz / STR amplifikasyon içeren geliştirilmiş bir amplifikasyon protokolü ile birlikte numune 'DNA dokunun', bir geri kazanıma müsaade etmek kısa tandem tekrarı (STR) biyo-parçacık verici (ler) profilleri. 

Video: Enhanced Genetic Analysis of Single Human Bioparticles Recovered by Simplified Micromanipulation from Forensic &#8216;Touch DNA&#8217; Evidence

Dissection of Hippocampal Dentate Gyrus from Adult Mouse

The hippocampus is one of the most widely studied areas in the brain because of its important functional role in memory processing and learning, its remarkable neuronal cell plasticity, and its involvement in epilepsy, neurodegenerative diseases, and psychiatric disorders. The hippocampus is composed of distinct regions; the dentate gyrus, which comprises mainly granule neurons, and Ammon's horn, which comprises mainly pyramidal neurons, and the two regions are connected by both anatomic and functional circuits. Many different mRNAs and proteins are selectively expressed in the dentate gyrus, and the dentate gyrus is a site of adult neurogenesis; that is, new neurons are continually generated in the adult dentate gyrus. To investigate mRNA and protein expression specific to the dentate gyrus, laser capture microdissection is often used. This method has some limitations, however, such as the need for special apparatuses and complicated handling procedures. In this video-recorded protocol, we demonstrate a dissection technique for removing the dentate gyrus from adult mouse under a stereomicroscope. Dentate gyrus samples prepared using this technique are suitable for any assay, including transcriptomic, proteomic, and cell biology analyses. We confirmed that the dissected tissue is dentate gyrus by conducting real-time PCR of dentate gyrus-specific genes, tryptophan 2,3-dioxygenase (TDO2) and desmoplakin (Dsp), and Ammon's horn enriched genes, Meis-related gene 1b (Mrg1b) and TYRO3 protein tyrosine kinase 3 (Tyro3). The mRNA expressions of TDO2 and Dsp in the dentate gyrus samples were detected at obviously higher levels, whereas Mrg1b and Tyro3 were lower levels, than those in the Ammon's horn samples. To demonstrate the advantage of this method, we performed DNA microarray analysis using samples of whole hippocampus and dentate gyrus. The mRNA expression of TDO2 and Dsp, which are expressed selectively in the dentate gyrus, in the whole hippocampus of alpha-CaMKII+/- mice, exhibited 0.037 and 0.10-fold changes compared to that of wild-type mice, respectively. In the isolated dentate gyrus, however, these expressions exhibited 0.011 and 0.021-fold changes compared to that of wild-type mice, demonstrating that gene expression changes in dentate gyrus can be detected with greater sensitivity. Taken together, this convenient and accurate dissection technique can be reliably used for studies focused on the dentate gyrus.

A dissection technique for removal of the dentate gyrus from adult mouse under a stereomicroscope was demonstrated in this video-recorded protocol.

The hippocampus is one of the most widely studied areas in the brain because of its important functional role in memory processing and learning, its ...

Direct Analysis of Single Cells by Mass Spectrometry at Atmospheric Pressure

Analysis of biochemicals in single cells is important for understanding cell metabolism, cell cycle, adaptation, disease states, etc. Even the same cell types exhibit heterogeneous biochemical makeup depending on their physiological conditions and interactions with the environment. Conventional methods of mass spectrometry (MS) used for the analysis of biomolecules in single cells rely on extensive sample preparation. Removing the cells from their natural environment and extensive sample processing could lead to changes in the cellular composition. Ambient ionization methods enable the analysis of samples in their native environment and without extensive sample preparation.1 The techniques based on the mid infrared (mid-IR) laser ablation of biological materials at 2.94 &mu;m wavelength utilize the sudden excitation of water that results in phase explosion.2 Ambient ionization techniques based on mid-IR laser radiation, such as laser ablation electrospray ionization (LAESI) and atmospheric pressure infrared matrix-assisted laser desorption ionization (AP IR-MALDI), have successfully demonstrated the ability to directly analyze water-rich tissues and biofluids at atmospheric pressure.3-11 In LAESI the mid-IR laser ablation plume that mostly consists of neutral particulate matter from the sample coalesces with highly charged electrospray droplets to produce ions. Recently, mid-IR ablation of single cells was performed by delivering the mid-IR radiation through an etched fiber. The plume generated from this ablation was postionized by an electrospray enabling the analysis of diverse metabolites in single cells by LAESI-MS.12 This article describes the detailed protocol for single cell analysis using LAESI-MS. The presented video demonstrates the analysis of a single epidermal cell from the skin of an Allium cepa bulb. The schematic of the system is shown in Figure 1. A representative example of single cell ablation and a LAESI mass spectrum from the cell are provided in Figure 2.

Single cell analysis is performed by mass spectrometry on plant and animal cells at atmospheric pressure by using a sharpened optical fiber to sample the cells for laser ablation electrospray ionization (LAESI) mass spectrometry.

Analysis of biochemicals in single cells is important for understanding cell metabolism, cell cycle, adaptation, disease states, etc. Even the same cell ...

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

The number of significant genetic associations with common complex traits is constantly increasing. However, most of these associations have not been understood at molecular level. One of the mechanisms mediating the effect of DNA variants on phenotypes is gene expression, which has been shown to be particularly relevant for complex traits1.
This method tests in a cellular context the effect of specific DNA sequences on gene expression. The principle is to measure the relative abundance of transcripts arising from the two alleles of a gene, analysing cells which carry one copy of the DNA sequences associated with disease (the risk variants)2,3. Therefore, the cells used for this method should meet two fundamental genotypic requirements: they have to be heterozygous both for DNA risk variants and for DNA markers, typically coding polymorphisms, which can distinguish transcripts based on their chromosomal origin (Figure 1). DNA risk variants and DNA markers do not need to have the same allele frequency but the phase (haplotypic) relationship of the genetic markers needs to be understood. It is also important to choose cell types which express the gene of interest. This protocol refers specifically to the procedure adopted to extract nucleic acids from fibroblasts but the method is equally applicable to other cells types including primary cells.
DNA and RNA are extracted from the selected cell lines and cDNA is generated. DNA and cDNA are analysed with a primer extension assay, designed to target the coding DNA markers4. The primer extension assay is carried out using the MassARRAY (Sequenom)5 platform according to the manufacturer's specifications. Primer extension products are then analysed by matrix-assisted laser desorption/ionization time of-flight mass spectrometry (MALDI-TOF/MS). Because the selected markers are heterozygous they will generate two peaks on the MS profiles. The area of each peak is proportional to the transcript abundance and can be measured with a function of the MassARRAY Typer software to generate an allelic ratio (allele 1: allele 2) calculation. The allelic ratio obtained for cDNA is normalized using that measured from genomic DNA, where the allelic ratio is expected to be 1:1 to correct for technical artifacts. Markers with a normalised allelic ratio significantly different to 1 indicate that the amount of transcript generated from the two chromosomes in the same cell is different, suggesting that the DNA variants associated with the phenotype have an effect on gene expression. Experimental controls should be used to confirm the results.

Genetic associations often remain unexplained at a functional level. This method aims to assess the effect of phenotype-associated genetic markers on gene expression by analyzing cells heterozygous for transcribed SNPs. The technology allows accurate measurement by MALDI-TOF mass spectrometry to quantify allele-specific primer extension products.

The number of significant genetic associations with common complex traits is constantly increasing. However, most of these associations have not been ...

Transduction of Human Cells with Polymer-complexed Ecotropic Lentivirus for Enhanced Biosafety

Stem and tumor cell biology studies often require viral transduction of human cells with known or suspected oncogenes, raising major safety issues for laboratory personnel. Pantropic lentiviruses, such as the commonly used VSV-G pseudotype, are a valuable tool for studying gene function because they can transduce many cell types, including non-dividing cells. However, researchers may wish to avoid production and centrifugation of pantropic viruses encoding oncogenes due to higher biosafety level handling requirements and safety issues. Several potent oncogenes, including c-Myc and SV40 large T antigen, are known to enhance production of induced pluripotent stem cells (iPSC). All other known iPSC-inducing genetic changes (OCT4, SOX2, KLF4, NANOG, LIN28, and p53 loss of function) also have links to cancer, making them of relatively high safety concern as well. 
While these cancer-related viruses are useful in studying cellular reprogramming and pluripotency, they must be used safely. To address these biosafety issues, we demonstrate a method for transduction of human cells with ecotropic lentivirus, with additional emphasis on reduced cost and convenient handling. We have produced ecotropic lentivirus with sufficiently high titer to transduce greater than 90% of receptor-expressing human cells exposed to the virus, validating the efficacy of this approach. 
Lentivirus is often concentrated by ultracentrifugation; however, this process takes several hours and can produce aerosols infectious to human biomedical researchers. As an alternative, viral particles can be more safely sedimented onto cells by complexation with chondroitin sulfate and polybrene (CS/PB). This technique increases the functional viral titer up to 3-fold in cells stably expressing murine retrovirus receptor, with negligible added time and cost. Transduction of human dermal fibroblasts (HDFs) is maximally enhanced using CS/PB concentrations approximately 4-fold lower than the optimal value previously reported for cancer cell lines, suggesting that polymer concentration should be titrated for the target cell type of interest. We therefore describe the use of methylthiazolyldiphenyl-tetrazolium bromide (MTT) to assay for polymer toxicity in a new cell type. We observe equivalent viability of HDFs after viral transduction using either polymer complexation or the standard dose of polybrene (PB, 6 &mu;g/ml), indicating minimal acute toxicity.
In this protocol, we describe the use of ecotropic lentivirus for overexpression of oncogenes in human cells, reducing biosafety risks and increasing the transduction rate. We also demonstrate the use of polymer complexation to enhance transduction while avoiding aerosol-forming centrifugation of viral particles.

Lentiviruses are a valuable research tool for exploring gene function; however, researchers may wish to avoid production of pantropic lentivirus encoding known or suspected oncogenes. As an alternative, we present a safer protocol for use of ecotropic lentivirus on human cells modified to express the ecotropic receptor mSlc7a1.

Stem and tumor cell biology studies often require viral transduction of human cells with known or suspected oncogenes, raising major safety issues for ...

Analysis of Single-cell Gene Transcription by RNA Fluorescent In Situ Hybridization (FISH)

Adhesion of Plasmodium falciparum infected erythrocytes (IE) to human endothelial receptors during malaria infections is mediated by expression of PfEMP1 protein variants encoded by the var genes.
The haploid P. falciparum genome harbors approximately 60 different var genes of which only one has been believed to be transcribed per cell at a time during the blood stage of the infection. How such mutually exclusive regulation of var gene transcription is achieved is unclear, as is the identification of individual var genes or sub-groups of var genes associated with different receptors and the consequence of differential binding on the clinical outcome of P. falciparum infections. Recently, the mutually exclusive transcription paradigm has been called into doubt by transcription assays based on individual P. falciparum transcript identification in single infected erythrocytic cells using RNA fluorescent in situ hybridization (FISH) analysis of var gene transcription by the parasite in individual nuclei of P. falciparum IE1.
Here, we present a detailed protocol for carrying out the RNA-FISH methodology for analysis of var gene transcription in single-nuclei of P. falciparum infected human erythrocytes. The method is based on the use of digoxigenin- and biotin- labeled antisense RNA probes using the TSA Plus Fluorescence Palette System2 (Perkin Elmer), microscopic analyses and freshly selected P. falciparum IE. The in situ hybridization method can be used to monitor transcription and regulation of a variety of genes expressed during the different stages of the P. falciparum life cycle and is adaptable to other malaria parasite species and other organisms and cell types.

Analysis of Single-cell Gene Transcription by RNA Fluorescent In Situ Hybridization FISH

Fluorescent in situ hybridization (FISH) to identify mRNA transcripts in individual cells allows analysis of polygenic activity such as the simultaneous transcription of more than one member of the var multigene family in Plasmodium falciparum infected erythrocytes 1. The technique is adaptable and can be used on different types of genes, cells and organisms.

Adhesion of Plasmodium falciparum infected erythrocytes (IE) to human endothelial receptors during malaria infections is mediated by expression of PfEMP1 ...

Generation of Human Cardiomyocytes: A Differentiation Protocol from Feeder-free Human Induced Pluripotent Stem Cells

In order to investigate the events driving heart development and to determine the molecular mechanisms leading to myocardial diseases in humans, it is essential first to generate functional human cardiomyocytes (CMs). The use of these cells in drug discovery and toxicology studies would also be highly beneficial, allowing new pharmacological molecules for the treatment of cardiac disorders to be validated pre-clinically on cells of human origin. Of the possible sources of CMs, induced pluripotent stem (iPS) cells are among the most promising, as they can be derived directly from readily accessible patient tissue and possess an intrinsic capacity to give rise to all cell types of the body 1. Several methods have been proposed for differentiating iPS cells into CMs, ranging from the classical embryoid bodies (EBs) aggregation approach to chemically defined protocols 2,3. In this article we propose an EBs-based protocol and show how this method can be employed to efficiently generate functional CM-like cells from feeder-free iPS cells.

Pluripotent stem cells, either embryonic or induced pluripotent stem (iPS) cells, constitute a valuable source of human differentiated cells, including cardiomyocytes. Here, we will focus on cardiac induction of iPS cells, showing how to use them to obtain functional human cardiomyocytes through an embryoid bodies-based protocol.

In order to investigate the events driving heart development and to determine the molecular mechanisms leading to myocardial diseases in humans, it is ...

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

Efforts to detect and investigate key oncogenic mutations have proven valuable to facilitate the appropriate treatment for cancer patients. The establishment of high-throughput, massively parallel "next-generation" sequencing has aided the discovery of many such mutations. To enhance the clinical and translational utility of this technology, platforms must be high-throughput, cost-effective, and compatible with formalin-fixed paraffin embedded (FFPE) tissue samples that may yield small amounts of degraded or damaged DNA. Here, we describe the preparation of barcoded and multiplexed DNA libraries followed by hybridization-based capture of targeted exons for the detection of cancer-associated mutations in fresh frozen and FFPE tumors by massively parallel sequencing. This method enables the identification of sequence mutations, copy number alterations, and select structural rearrangements involving all targeted genes. Targeted exon sequencing offers the benefits of high throughput, low cost, and deep sequence coverage, thus conferring high sensitivity for detecting low frequency mutations.

We describe the preparation of barcoded DNA libraries and subsequent hybridization-based exon capture for detection of key cancer-associated mutations in clinical tumor specimens by massively parallel "next generation" sequencing. Targeted exon sequencing offers the benefits of high throughput, low cost, and deep sequence coverage, thus yielding high sensitivity for detecting low frequency mutations.

Efforts  to detect and investigate key oncogenic mutations have proven valuable to  facilitate the appropriate treatment for cancer patients. The ...

Alternative Cultures for Human Pluripotent Stem Cell Production, Maintenance, and Genetic Analysis

Human pluripotent stem cells (hPSCs) hold great promise for regenerative medicine and biopharmaceutical applications. Currently, optimal culture and efficient expansion of large amounts of clinical-grade hPSCs are critical issues in hPSC-based therapies. Conventionally, hPSCs are propagated as colonies on both feeder and feeder-free culture systems. However, these methods have several major limitations, including low cell yields and generation of heterogeneously differentiated cells. To improve current hPSC culture methods, we have recently developed a new method, which is based on non-colony type monolayer (NCM) culture of dissociated single cells. Here, we present detailed NCM protocols based on the Rho-associated kinase (ROCK) inhibitor Y-27632. We also provide new information regarding NCM culture with different small molecules such as Y-39983 (ROCK I inhibitor), phenylbenzodioxane (ROCK II inhibitor), and thiazovivin (a novel ROCK inhibitor). We further extend our basic protocol to cultivate hPSCs on defined extracellular proteins such as the laminin isoform 521 (LN-521) without the use of ROCK inhibitors. Moreover, based on NCM, we have demonstrated efficient transfection or transduction of plasmid DNAs, lentiviral particles, and oligonucleotide-based microRNAs into hPSCs in order to genetically modify these cells for molecular analyses and drug discovery. The NCM-based methods overcome the major shortcomings of colony-type culture, and thus may be suitable for producing large amounts of homogeneous hPSCs for future clinical therapies, stem cell research, and drug discovery.

Here, we present human pluripotent stem cell (hPSC) culture protocols, based on non-colony type monolayer (NCM) growth of dissociated single cells. This new method, utilizing Rho-associated kinase inhibitors or the laminin isoform 521 (LN-521), is suitable for producing large amounts of homogeneous hPSCs, genetic manipulation, and drug discovery.

Human pluripotent stem cells (hPSCs) hold great promise for regenerative medicine and biopharmaceutical applications. Currently, optimal culture and ...

Fecal Glucocorticoid Analysis: Non-invasive Adrenal Monitoring in Equids

Adrenal activity can be assessed in the equine species by analysis of feces for corticosterone metabolites. During a potentially aversive situation, corticotrophin releasing hormone (CRH) is released from the hypothalamus in the brain. This stimulates the release of adrenocorticotrophic hormone (ACTH) from the pituitary gland, which in turn stimulates release of glucocorticoids from the adrenal gland. In horses the glucocorticoid corticosterone is responsible for several adaptations needed to support equine flight behaviour and subsequent removal from the aversive situation. Corticosterone metabolites can be detected in the feces of horses and assessment offers a non-invasive option to evaluate long term patterns of adrenal activity. Fecal assessment offers advantages over other techniques that monitor adrenal activity including blood plasma and saliva analysis. The non-invasive nature of the method avoids sampling stress which can confound results. It also allows the opportunity for repeated sampling over time and is ideal for studies in free ranging horses. This protocol describes the enzyme linked immunoassay (EIA) used to assess feces for corticosterone, in addition to the associated biochemical validation.

Adrenal activity can be assessed in the equine species by analysis of feces for corticosterone metabolites. The method offers a non-invasive option to assess long term patterns in both domestic and free ranging horses. This protocol describes the enzyme linked immunoassay involved and the associated biochemical validation.

Adrenal activity can be assessed in the equine species by analysis of feces for corticosterone metabolites. During a potentially aversive situation, ...

Laboratory Protocol for Genetic Gut Content Analyses of Aquatic Macroinvertebrates Using Group-specific rDNA Primers

Analyzing food webs is essential for a better understanding of ecosystems. For example, food web interactions can undergo severe changes caused by the invasion of non-indigenous species. However, an exact identification of field predator-prey interactions is difficult in many cases. These analyses are often based on a visual evaluation of gut content or the analysis of stable isotope ratios (&#948;15N and &#948;13C). Such methods require comprehensive knowledge about, respectively, morphologic diversity or isotopic signature from individual prey organisms, leading to obstacles in the exact identification of prey organisms. Visual gut content analyses especially underestimate soft bodied prey organisms, because maceration, ingestion and digestion of prey organisms make identification of specific species difficult. Hence, polymerase chain reaction (PCR) based strategies, for example the use of group-specific primer sets, provide a powerful tool for the investigation of food web interactions. Here, we describe detailed protocols to investigate the gut contents of macroinvertebrate consumers from the field using group-specific primer sets for nuclear ribosomal deoxyribonucleic acid (rDNA). DNA can be extracted either from whole specimens (in the case of small taxa) or out of gut contents of specimens collected in the field. Presence and functional efficiency of the DNA templates need to be confirmed directly from the tested individual using universal primer sets targeting the respective subunit of DNA. We also demonstrate that consumed prey can be determined further down to species level via PCR with unmodified group-specific primers combined with subsequent single strand conformation polymorphism (SSCP) analyses using polyacrylamide gels. Furthermore, we show that the use of different fluorescent dyes as labels enables parallel screening for DNA fragments of different prey groups from multiple gut content samples via automated fragment analysis.

Most common gut content analyses of macroinvertebrates are visual. Requiring intense knowledge about morphological diversity of prey organisms, they miss soft bodied prey and, due to strong comminution of prey, are nearly impossible for some organisms, including amphipods. We provide detailed, novel genetic approaches for macroinvertebrate prey identification in the diet of amphipods.

Analyzing food webs is essential for a better understanding of ecosystems. For example, food web interactions can undergo severe changes caused by the ...