Apr 23, 2025
Version 2
Sample Preparation for Quantitative Whole Cell Proteome Analysis by Mass Spectrometry V.2
- 1Sascha Martens lab, University of Vienna, Max Perutz Labs - Vienna
Protocol Citation: Elias Adriaenssens 2025. Sample Preparation for Quantitative Whole Cell Proteome Analysis by Mass Spectrometry. protocols.io https://dx.doi.org/10.17504/protocols.io.n92ld5918v5b/v2Version created by Elias Adriaenssens
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
Created: April 23, 2025
Last Modified: April 23, 2025
Protocol Integer ID: 141123
Keywords: ASAPCRN, sample preparation for quantitative whole cell proteome analysis, quantitative whole cell proteome analysis, mass spectrometry, mass spectrometry this protocol, sample preparation, samplespecific volume, experiment specific note, internal electronic lab notebook, sample, preparation, automatic generation process, cell
Funders Acknowledgements:
Aligning Science Across Parkinson’s (ASAP)
Grant ID: ASAP-000350
Marie Skłodowska-Curie MSCA Postdoctoral fellowship
Grant ID: 101062916
Abstract
This protocol was generated from an internal electronic lab notebook and contains experiment specific notes, for example, samplespecific volumes and incubation times. Due to the automatic generation process it might also contain errors and should be interpreted cautiously. An updated protocols will still be uploaded.This protocol was generated from an internal electronic lab notebook and contains experiment specific notes, for example, sample-specific volumes and incubation times. Due to the automatic generation process it might also contain errors and should be interpreted cautiously. An updated protocols will still be uploaded.
Guidelines
GENERAL NOTE: This protocol was generated from an internal electronic lab notebook and contains experiment specific notes, for example, sample-specific volumes and incubation times. Due to the automatic generation process it might also contain errors and should be interpreted cautiously. An updated protocols will still be uploaded.
Materials
Buffer: 2% SDC 100 millimolar (mM) Tris/HCl pH=8.8 (20 mg SDC in 1 mL )
- PBS
- sodium deoxycholate
- Tris/HCl pH 8.8
- benzonase
- micro BCA assay (Thermo Fisher)
- iodoacetamide
- DTT
- ammonium bicarbonate
- LysC (mass spectrometry grade, FUJIFILM Wako chemicals)
- trypsin (Trypsin Gold, Promega)
- trifluoroacetic acid
Safety warnings
This protocol was generated from an internal electronic lab notebook and contains experiment specific notes, for example, sample-specific volumes and incubation times. Due to the automatic generation process it might also contain errors and should be interpreted cautiously. An updated protocols will still be uploaded.This protocol was generated from an internal electronic lab notebook and contains experiment specific notes, for example, sample-specific volumes and incubation times. Due to the automatic generation process it might also contain errors and should be interpreted cautiously. An updated protocols will still be uploaded.
Cell Lysis
33m
Pre-heat 2% sodium deoxycholate (SDC) 100 millimolar (mM) Tris/HCl pH 8.8 at 95 °C .
Add 50 µL hot 2% SDC 100 millimolar (mM) Tris to cell pellet (add more if not soluble).
Incubate samples for 00:10:00 at 95 °C .
10m
Resuspend thoroughly with pipet, put to 95 °C for 00:03:00 .
3m
Cool down, add 1 µL benzonase and incubate On ice for 10-30 min.
Sonicate 5 cycles 30/30 sec level H in Bioruptor.
Let sit for 00:10:00 for extra benzonase treatment.
10m
Centrifuge at 15000 x g, 10°C, 00:10:00 to pellet cell debris.
10m
Transfer supernatant to fresh 0.6mL tube.
Determine protein concentration with micro BCA assay.
Note
NOTE: we use the Micro BCA kit according to manufacturer’s instructions https://www.thermofisher.com/order/catalog/product/23235.
In Solution Digest
4h 39m
Protein concentration: ~ 5 µL .
Transfer 50 µg protein to 0.2mL tube, fill up to 15 µL .
Reduction: 10 millimolar (mM) DTT (250 millimolar (mM) stock) 00:30:00 50 °C . Here we used0.6 µL of DTT.
30m
Alkylation: 20 millimolar (mM) iodoacetamide (IAA) (500 millimolar (mM) stock = 0.092 µL ) 00:30:00 Room temperature in the dark. Here we used0.6 µL of IAA.
30m
Quench the remaining iodoacetamide (IAA) with half amount of DTT used in step 14 and incubate for 00:10:00 at Room temperature . Here we used0.3 µL DTT to quench.
10m
Dilute to 1% final SDC concentration with 100 millimolar (mM) Tris pH 8.5 . Here we used 15 µL of SDC.
Add 1:100 LysC (100 µL aliquot) – incubate at Room temperature for up to 03:00:00 . Here we used 0.5 µL from 1 µL .
3h
Add 1:50 Trypsin (100 µL aliquot) – incubate at 37 °C Overnight . Here we used 1 µL from 1 µL . Here, the total volume was 33 µL at this point of the protocol.
Add 10% TFA to reach final 1% TFA, vortex, spin down at 14000 rpm, 00:10:00 . For us here, we added 3.3 µL to reach 10% TFA.
10m
Transfer supernatant to new tube.
Add 10% TFA to reach final 2% TFA, vortex, spin down at 14000 rpm, 00:10:00 . Here we added 3.3 µL , to reach a total volume of 39.6 µL .
10m
Load directly onto prepared C18 STAGEtip or transfer to new tube and load 20%. For us here, 20% equals 10 µg -> 8 µL .
Desalt: Load the peptides on a C18 STAGEtip.
Note
3-5 plugs depending on protein amount, 3 plugs for max. 20 µg .
Equilibrate:
100 µL 100% MeOH, spin 2000 rpm, 00:03:00 .
3m
100 µL 80% ACN, 0.1% TFA, spin 2000 rpm, 00:03:00 .
3m
100 µL 0.1% TFA, spin 2000 rpm, 00:03:00 .
3m
Load sample: spin 1700 rpm .
Wash: 100 µL 0.1% TFA -> keep flow through (FT) and wash together.
Elute: 2x30 µL 60% ACN, 0.1% TFA in PCR tube.
Speedvac to remove ACN and take up sample in 20 µL 0.1% TFA 2% ACN.