Polycarbonate Ultracentrifuge Tube Re-Use in Proteomic Analyses of Extracellular Vesicles

Summary

A detailed protocol is provided for cleaning and re-using polycarbonate ultracentrifuge tubes to perform extracellular vesicle isolation suitable for proteomics experiments.

Abstract

Single-use laboratory plastics exacerbate the pollution crisis and contribute to consumable costs. In extracellular vesicle (EV) isolation, polycarbonate ultracentrifuge (UC) tubes are used to endure the associated high centrifugal forces. EV proteomics is an advancing field and validated re-use protocols for these tubes are lacking. Re-using consumables for low-yield protein isolation protocols and downstream proteomics requires reagent compatibility with mass spectroscopy acquisitions, such as the absence of centrifuge tube-derived synthetic polymer contamination, and sufficient removal of residual proteins.

This protocol describes and validates a method for cleaning polycarbonate UC tubes for re-use in EV proteomics experiments. The cleaning process involves immediate submersion of UC tubes in H₂O to prevent protein drying, washing in 0.1% sodium dodecyl sulfate (SDS) detergent, rinsing in hot tap water, demineralized water, and 70% ethanol. To validate the UC tube re-use protocol for downstream EV proteomics, used tubes were obtained following an experiment isolating EVs from cardiovascular tissue using differential UC and density gradient separation. Tubes were cleaned and the experimental process was repeated without EV samples comparing blank never-used UC tubes to cleaned UC tubes. The pseudo-EV pellets obtained from the isolation procedures were lysed and prepared for liquid chromatography-tandem mass spectrometry using a commercial protein sample preparation kit with modifications for low-abundance protein samples.

Following cleaning, the number of identified proteins was reduced by 98% in the pseudo-pellet versus the previous EV isolation sample from the same tube. Comparing a cleaned tube against a blank tube, both samples contained a very small number of proteins (≤20) with 86% similarity. The absence of polymer peaks in the chromatograms of the cleaned tubes was confirmed. Ultimately, the validation of a UC tube cleaning protocol suitable for the enrichment of EVs will reduce the waste produced by EV laboratories and lower the experimental costs.

Introduction

Extracellular vesicles (EVs) are lipid-bilayer-delimited particles released from cells that carry biologically active cargo, such as protein, and participate in various biological processes, including cell-cell communication and the formation of biologic mineralization¹. These particles are found in all body fluids and tissues, and their biological activities and uses are a rapidly evolving field of scientific research. Isolation and validation of these nanoparticles present various challenges due to their small size and bio-similarity to other particles, such as liposomes and protein aggregates. The most recent International Society of Extracellular Vesicles guidelines, Minimal information for studies of extracellular vesicles 2018 (MISEV2018), are the recognized standard for EV scientific research².

Various methods, often in tandem, must be used for EV isolation depending on the upstream source and the downstream applications. As of 2015, the most common primary isolation method for EVs was differential ultracentrifugation (UC)². In principle, initial lower speed centrifugation separates larger or denser unwanted components, such as cells and cell debris, leaving EVs in the supernatant. Subsequently, UC uses very high centrifugal force to pellet out and thus separate and purify EVs from other particles that are smaller or less dense but which may also contain dense non-EV particles. Most protocols will often use, at one step or another, UC to isolate EVs from a fluid³. Further, UC is used in other methods of EV isolation, such as density gradient ultracentrifugation (DGUC), which uses mediums such as Optiprep^TM iodixanol and centrifugal force to separate EVs according to their buoyant density⁴. Other methods of EV isolation exist³.

Considering the rapidly evolving understanding of the biological processes dictated by EVs and their potential as biomarkers and information regarding pathophysiology, discovery-based analyses such as proteomics have gained traction^5,6,7,8. EVs are small, and, depending on the source, have a low yield of protein (<1 μg) when compared to whole tissue or cell lysate. Isolation of EVs for proteomics analysis requires special considerations, such as the removal of non-EV protein contaminants from upstream liquid or tissue, consideration of EV protein degradation during the isolation process, and the utilization of methods that create protein solutions that are chemically compatible with peptide preparation and mass spectrometry analyses.

Research laboratory consumables are often plastic and disposable in nature. These single-use materials contribute to the global plastic pollution crisis and consumable costs. Specialized polycarbonate and polystyrene UC tubes are designed to withstand the high centrifugal forces required to pellet EVs in laboratory applications. While it is possible to sterilize and disinfect UC tubes for re-use, proteomic analysis, especially those of low protein yields such as EVs, requires special attention. Not only is sufficient removal of residual protein from the previous use paramount, chemical compatibility with mass-spectroscopy and plastic-derived polymer contamination must also be considered.

Here we present a cleaning protocol of polycarbonate tubes using detergents suitable for mass-spectrometry and perform experiments to validate its successful removal of residual protein below limits of detection and lack of detectable polymer contaminants. To validate the cleaning protocol for EV proteomic applications using both UC and DGUC purposes, we obtained tubes from isolations of human vasculature tissue EVs with a combined UC and DGUC protocol. Tubes were cleaned using the protocol described, and the experimental process was repeated without samples comparing a blank never-used UC tube and a cleaned UC tube. Ultimately, the validation of a UC tube cleaning protocol suitable for the enrichment of EVs will reduce the waste produced by EV laboratories and lower the cost associated with such experiments.

Protocol

1. Tube cleaning

NOTE: The EV isolation procedure uses both capped and uncapped polycarbonate UC tubes (detailed below). The same procedure was followed for both capped and uncapped tubes. In the case of capped tubes, the lid parts were cleaned individually and reassembled post drying and pre-storage.

1. Following the initial use of the polycarbonate tubes and removal of the sample, immediately submerge UC tubes in tap water to prevent drying of the sample to the side of the tube.
2. Transfer and submerge tubes in 0.1% sodium dodecyl sulfate (SDS) in tap water for 10 min.
3. One tube at a time, decant most, but not all, of the SDS solution from the tube and use a cotton swab to thoroughly wipe the area of the tube where the EV pellet was located.
   NOTE: Do not use anything with bristles. This protocol used normal cotton swabs; however, specialized, low-lint cotton swabs can be used for cleaning the tubes.
4. Rinse at least 3x with hot tap water (~50 °C). Make sure to fill and decant the tube completely.
5. Rinse 1x with demineralized water using a spray bottle or a narrow-mouthed wash bottle.
6. Rinse 1x with 70% ethanol using a spray bottle.
7. Leave the tube upside down to dry.
   NOTE: Tube racks for fluorescence activated cell sorting work well for drying the UC tubes.
8. Place the completely dried tubes in a clean jar; they are ready for reuse.
   NOTE: Currently, the protocol is validated for re-use up to 2x.

2. EV enrichment

NOTE: The following EV isolation and proteomics protocol was used for both the original tissue EV isolation, as well as the "mock samples" used to obtain the blank (never-used) and cleaned tube samples. The original samples were resuspended tissue-entrapped EVs from carotid plaques of patients who underwent carotid endarterectomies. Surgical specimens were collected from the University Health Network (Toronto, Canada) and was approved by the institutional ethics committee. All patients provided informed consent for sample collection and data analysis, in accordance with the Declaration of Helsinki. The mock samples were pseudo-pellets obtained from treating blank and cleaned tubes with the same solutions and processing steps as the EV isolation samples.

1. Defrost EV samples or mock samples in PBS on ice.
2. Make NTE buffer (10 mM Tris-HCl, 1 mM EDTA, 0.137 M NaCl pH 7.4) and sterile filter.
3. Spin the samples at 10,000 × g for 10 min at 4 °C.
4. Move the supernatant into a 1 mL open-top polycarbonate tube.
5. Centrifuge the supernatant at 100,000× g for 1 h at 4 °C.
6. Resuspend the pellet in 150 µL of sterile-filtered NTE buffer with protease inhibitor.
7. Transfer to a 1.5 mL microcentrifuge tube and add NTE buffer to reach a total sample volume of 1.5 mL.
8. Keep the samples on ice.

3. Preparation of density gradients and density gradient separation

NOTE: This EV isolation protocol has been previously described by Blaser et al.⁹ In brief:

1. Prepare five solutions of Iodixanol Density Gradient Medium (10%, 15%, 20%, 25%, and 30%) with NTE buffer as a diluent.
2. Layer the five density solutions sequentially in capped ultracentrifuge tube(s) with 30% at the bottom and 10% on the top.
3. Secure the caps on the tube(s) and move gently to a stable horizontal position for 1 h at room temperature.
4. After 1 h, move the tube(s) gently to a vertical position on ice for 30 min to cool the gradient.
5. Add 1.5 mL of the sample or mock sample (NTE buffer) to the top of the prepared density gradient tube(s).
6. Ultracentrifuge tube(s) at 250,000 × g for 40 min at 4 °C.
7. Remove the top fractions of the density gradient (2.4 mL) to uncapped ultracentrifuge tube(s). Fill to 9 mL with sterile-filtered NTE buffer.
8. Pellet the EVs by ultracentrifuging at 100,000 × g for 1 h at 4 °C.
   NOTE: Circle the location of the visible EV pellet or expected location with a marker. This will allow you to clean the area of the pellet with the swab directly.
9. Aspirate the supernatant while moving the tube into an upside-down position for 3 min. Remove the remaining droplets with a cotton swab before turning the tube right side up.
10. Resuspend the EV pellet in 12 µL of lyse buffer in the referenced kit.

4. Peptide preparation for proteomics

NOTE: Proteomics sample preparation was performed according to the kit protocol with in-house modifications for low-abundance protein samples. The modified protocol is as follows:

1. Lyse, denature, reduce, and alkylate the samples by heating in lyse buffer at 95 °C for 10 min.
2. Digest the samples using the Lys-C/trypsin digest solution for 2 h at 37 °C using 10 µL of lyse solution from the sample and 10 µL of the digest solution.
3. Purify peptides through a cartridge by washing hydrophilic and hydrophobic contaminants out and eluting off purified peptides using kit solutions.
4. Dry the purified peptides in a speed vacuum at 45 °C for 45 min or until dry.
   NOTE: Avoid overdrying of the peptides.
5. Store samples at -80 °C until the time of mass spectrometry sequencing.
6. Add 17 µL of LC-load solution to the dried peptides.
7. Leave the samples on ice for 1 h.
8. Vortex the samples briefly and then sonicate in an ultrasonic waterbath for 5 min.
9. Centrifuge the LC-load samples at 16,000 × g for 1 min, aspirate 15 µL from the top, and separate into a new tube.

5. Liquid chromatography and tandem mass spectrometry sequencing

1. Inject 2 µL of LC-load peptide solution onto a mass spectrometer.
2. Fractionate the peptides using a dual-column setup.
3. Heat the column at a constant temperature of 45 ˚C.
4. Run the analytical gradient at 300 nL/min from 5% to 21% Solvent B (acetonitrile/0.1% formic acid) for 60 min, followed by 10 min of 21% to 30% Solvent B, and another 10 min of a 95%-5% jigsaw wash.
5. Set the MS1 to 120 K resolution (maximum injection time, 25 ms), subject the top precursor ions (within a 3.0 s cycle time) to HCD isolation width 1.2 m/z, dynamic exclusion enabled (60 s), and set the MS2 resolution to 60 K (maximum injection time, auto; normalized collision energy, 24%, 26%, and 28%).
6. Set the MS1 and MS2 acquisition range to 400 m/z-1,200 m/z and 120 m/z-1,200 m/z, respectively.

6. Peptide/protein identification

1. Search the acquired peptide spectra with a proteomic search software using a commercial search algorithm against a human uniProt database.
2. Set the digestion enzyme to trypsin and allow up to two missed cleavages.
3. Set the precursor tolerance to 10 ppm and the fragment tolerance window to 0.02 Da.
4. Set methionine oxidation and N-terminal acetylation as variable modifications and cysteine carbamidomethylation as fixed modification.
5. Filter the peptides based on a false discovery rate (FDR) threshold of 1.0% as calculated by the Percolator algorithm.
6. Only consider peptides assigned to one given protein group and not detected in any other protein group as unique and use them for further analyses.
7. Only include a minimum of two unique peptides for each protein in the analyses.
8. Maximize IDs with precursor ion detection.
9. Perform chromatographic alignment with a maximum retention time shift of 10 min, mass tolerance of 10 ppm, and signal-to-noise minimum of 5.
10. Normalize peptide abundance by total peptide amount.

Results

To validate the cleaning protocol (Figure 1), two experiments were performed. First, the proteome of the "mock sample" from the cleaned tube was compared against the proteome of the tissue EV sample from the tube's initial use to determine the carryover of identified proteins. Representative chromatograms show a reduction in peak heterogeneity following cleaning of the tubes (Figure 2). In the original EV isolation, 806 proteins were identified with ...

Discussion

Here we describe and validate a protocol for cleaning polycarbonate UC tubes for EV enrichment and proteomic applications. We demonstrated the successful removal of residual protein from the previous UC tube sample compared with a cleaned pseudo-pellet analysis below the limit of detection of this mass spectrometry acquisition protocol and showed the proteomic similarity of blank never-used UC tube compared to cleaned UC tube pseudo pellets.

First, to prevent the inadvertent adsorption of prot...

Materials

Name	Company	Catalog Number	Comments
10 mL Open-Top Thickwall Polycarbonate Tube	Beckman Coulter Life Sciences	355630	uncapped ultracentrifuge tube(s)
10.4 mL Polycarbonate Bottle with Cap Assembly	Beckman Coulter Life Sciences	355603	capped ultracentrifuge tube(s)
an Acclaim PepMap 100 C18 HPLC Columns, 75 µm x 70 mm; and an EASY-Spray HPLC Column, 75 µm x 250 mm	ThermoFisher Scientific	164946 and ES902	Dual column setup
Critical Swab Swab, Cotton Head	VWR	89031-270	cotton swab
Exploris 480 fronted with EASY-Spray Source, coupled to an Easy-nLC1200 HPLC pump.	ThermoFisher Scientific	BRE725533	Mass spectrometer
Human UniProt database (101043 entries, updated January 2022)	NA	NA	Human database
MilliQ water			water
PreOmics iST kit	PreOmics	P.O.00027	commercial protein sample preparation kit
Proteome Discoverer  package (PD, Version 2.5)	ThermoFisher Scientific	NA	Proteomic search software
SEQUEST-HT search algorithm	NA	NA	Search algorithm
Sodium Dodecyl Sulfate (20%)	Boston BioProducts	BM-230	detergent