Jun 22, 2020
Chloroform-Methanol Protein Extraction with Zymolyase Treatment for Yeast (High Throughput)
- 1Lawrence Berkeley National Laboratory
- LBNL omics
- Yeast Protocols, Tools, and Tips
External link: https://pubs.acs.org/doi/abs/10.1021/acs.jproteome.9b00455
Protocol Citation: Jennifer Gin, Yan Chen, Christopher J Petzold 2020. Chloroform-Methanol Protein Extraction with Zymolyase Treatment for Yeast (High Throughput). protocols.io https://dx.doi.org/10.17504/protocols.io.bhptj5nn
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
We use this protocol and it's working
Created: June 18, 2020
Last Modified: June 22, 2020
Protocol Integer ID: 38355
Keywords: Proteomics, Sample preparation, Bacteria, Protein quantification, Protein extraction, Trypsin digestion,
Abstract
We adapted a high-throughput sample preparation workflow for Gram-negative bacteria to work with yeast. It consists of a zymolyase cell wall digestion step, cell lysis, protein precipitation, protein resuspension, protein quantification, and normalization of protein concentration followed by standard bottom-up proteomic procedures of reducing and blocking cysteine residues and tryptic digestion.
This protocol was adapted from the manual sample preparation method found in Chen, Y., et al. "Automated “Cells-To-Peptides” Sample Preparation Workflow for High-Throughput, Quantitative Proteomic Assays of Microbes."Journal of proteome research 18.10 (2019): 3752-3761.
Guidelines
- All centrifuge steps use an Eppendorf 5810R centrifuge.
- A Molecular Devices Spectramax 250 microplate reader is used for the protein quantification assay measurement.
- Tryptic digestion is accomplished in an AB Sciex Veriti 96-well thermocycler.
Notes:
- For fewer than 30 samples PCR strips are easier to handle than plates, but once the number of samples is greater than 30 we find that a plate is a better choice.
- A multi-channel pipette is recommended for large numbers of samples.
- Measuring the amount of cells by multiplying the OD of the culture by the volume of the culture provides a good estimate for most applications, but the amount of cells can be determined more accurately from dry cell weight (DCW) or cell counting methods.
- We typically extract over 100 ug of protein from 2.0 OD*mLs of cells, so adjust the starting amount of cells for your organism or culturing conditions.
Materials
MATERIALS
SorbitolP212121
Corning™ 96-Well Solid Black Polystyrene Microplates (Costar 3915)Fisher ScientificCatalog #07-200-590
EDTAThermo FisherCatalog #17892
Pierce™ Bovine Serum Albumin Standard Pre-Diluted SetThermo FisherCatalog #23208
Tris(2-carboxyethyl)phosphine hydrochloride (TCEP)Sigma AldrichCatalog #C4706
IodoacetamideMillipore SigmaCatalog #I1149
ZymolyaseZymo ResearchCatalog #E1005
Methanol LC-MS grade B&J BrandVWR ScientificCatalog #BJLC230-2.5
Chloroform for HPLCSigma – AldrichCatalog #34854
Water LC-MS grade B&J BrandVWR ScientificCatalog #BJLC365-2.5
Ammonium Bicarbonate LC-MS gradeVWR ScientificCatalog #BJ40867-50G
DC Protein Assay Reagent ABio-rad LaboratoriesCatalog #500-0113
DC Protein Assay Reagent BBio-rad LaboratoriesCatalog #500-0114
8-strip PCR Tubes with CapsAxygenCatalog #14-222-251
TrypsinSigma AldrichCatalog #T6567-1MG
PCR Plate 96-well non-skirtedThermo Fisher ScientificCatalog #AB0600
Thermo Scientific Autosampler Vial KitThermo Fisher ScientificCatalog #03-060-016
Eppendorf Snap-Cap Microcentrifuge Flex-Tube Tubes AmberFisher ScientificCatalog #05-402-31
Hard-Shell 96-Well PCR Plates low profile thin wall skirted white/clearBIO-RADCatalog #HSP9601
Safety warnings
Chloroform is used in this protocol so please follow the appropriate safety guidelines for handling and disposing of halogenated solvents at your institution and use a fume hood for steps involving chloroform.
Wear gloves and appropriate PPE for safety and to minimize contamination of samples.
Before start
This protocol consists of steps for:
- Protein extraction from yeast cells
- Protein quantification
- Tryptic digestion
For this protocol you will need:
- an Eppendorf 5810R centrifuge with S-4-104 rotor or similar centrifuge
- a Molecular Devices Spectramax 250 microplate reader or similar plate reader
- an AB Sciex Veriti 96-well thermocycler or a similar incubator
Zymolyase cell wall treatment
Zymolyase cell wall treatment
30m
30m
Thaw cells at Room temperature
Note
Note: If transferring directly from active cultures, omit this step. Adapt as needed for your specific organism and culturing conditions.
Transfer 2-4 OD*mLs of cells to 8-Strip PCR tubes (Axygen, Cat.#14-222-251) or a 96-well PCR plate (ThermoFisher, Cat.#AB0600).
A strip of PCR tubes filled 30-40% full of cell pellet is approximately 10-20 OD*mLs of cells.
Buffer to prepare:
• Prepare Zymolyase Buffer by dissolving 1.822 g Sorbitol and 0.292 g Ethylenediaminetetraacetic acid (EDTA) in 10 mL Water
Add 1.5 µL (7.5 U) of Zymolyase to 200 µL Zymolyase Buffer before resuspending the cells with it.
Incubate in 37 °C water bath (Thermo Fisher Scientific, Cat.#TSGP2S) for 00:10:00 to digest cell walls.
Centrifuge at 4000 rpm, 25°C, 00:01:00 then remove the supernatent.0 µL
Protein extraction
Protein extraction
30m
30m
Add 80 µL of LC-MS grade Methanol (VWR Scientific, Cat.#BJLC230-2.5). Pipet to resuspend well.
Add 20 µL of Chloroform (Sigma-Aldrich, Cat.#34854). Pipet/vortex to mix.
Safety information
Use a fume hood when handling and pipetting chloroform.
Add 60 µL of LC-MS grade Water (VWR Scientific, Cat.#BJLC365-2.5). Pipet/vortex to mix.
Centrifuge at 4000 rpm, 25°C, 00:01:00 .
Carefully remove the top layer of solvent (Methanol + Water) by pipetting.
Add 100 µL of Methanol.
Note
Tip: Break up the protein pellet by piercing it with the pipet tip, and add Methanol to the bottom of the tube or plate.
Centrifuge at 4000 rpm, 25°C, 00:02:00 .
Carefully discard solvent (Methanol + Chloroform).
Safety information
Discard in an appropriate waste container for halogenated solvents.
Air-dry for 00:05:00 .
Note
Tip: Do not dry for longer than 00:45:00 or the pellet will be difficult to resuspend.
Safety information
Dry samples in a fume hood.
5m
Resuspend with 60 µL 100 millimolar (mM) Ammonium bicarbonate in 20% Methanol .
Note
Note: Samples are typically cloudy in this step. After trypsin digestion they will be nearly clear.
Store at -20 °C until ready for Protein Quantitation Assay.
Protein Quantitation Assay (Lowry Method)
Protein Quantitation Assay (Lowry Method)
30m
30m
Dilute samples 10 fold by adding 5 µL Protein sample, mix well right before transfer to45 µL Water in 8-Strip PCR tubes or 96-well plate.
Note
Note: The protein concentration can be determined by using several methods that are available in kits. We use the Bio-Rad DC Protein Assay (Bio-rad Laboratories, Cat.#500-0113, Cat.#500-0114) but the Bradford protein quantification assay is also commonly used. The accuracy of most protein concentration measurements can be variable, thus it is important to minimize differences in sample handling and to use replicates when quantifying the amount of protein in a sample.
Transfer 2 replicates of each of the following to Corning 96-Well Black Polystyrene Microplate (Fisher Scientific, Cat.#07-200-590):
5 µL Water (Blank)
5 µL Pierce Bovine Serum Albumin Standard Pre-Diluted Set (Std) (ThermoFisher, Cat.#23208)
5 µL Diluted samples, mix well right before adding to plate (Example 1-20)
| Blank | Std 1 | Std 2 | Std 3 | Std 4 | Std 5 | Std 6 | Std 7 | |||||
| Blank | Std 1 | Std 2 | Std 3 | Std 4 | Std 5 | Std 6 | Std 7 | |||||
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
| 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | |||||
| 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | |||||
Example Plate with 20 samples
Add 25 µL Bio-Rad DC Protein Assay Reagent A (Bio-rad Laboratories, Cat.#500-0113) and wait 00:05:00 .
.
Add 200 µL Bio-Rad DC Protein Assay Reagent B (Bio-rad Laboratories, Cat.#500-0114) and wait 00:10:00 .
.
Read plate in the microplate reader (280 nm) and calculate protein concentrations.
Trypsin Digestion (5h - 16h)
Trypsin Digestion (5h - 16h)
5h
5h
Chemicals to prepare:
• Prepare 100 millimolar (mM) Tris(2-carboxyethyl)phosphine (TCEP) solution by dissolving 28.7 mg TCEP in 1 mL 100mM Ammonium Bicarbonate
• Prepare 200 millimolar (mM) Iodoacetamide (IAA) solution by dissolving 36.8 mg Iodoacetamide in 1 mL 100mM Ammonium Bicarbonate
•Prepare 1 mg/mL Trypsin by adding 1 mL 1mM HCl to 1 mg Trypsin
Note
Store TCEP, IAA, and Trypsin in -20C.
IAA is light sensitive. Store in amber tube (Fisher Scientific, Cat.#05-402-31).
15m
Dilute protein samples to 2.4 µg/µL in 100 millimolar (mM) Ammonium Bicarbonate (AMBIC)
Note
Mix protein well before you dilute it.
Mix protein with TCEP, IAA, and trypsin in 100 millimolar (mM) Ammonium Bicarbonate (AMBIC) .
Note
The final concentrations will be 2 µg/µL protein (in 50 ul total volume) , 5 millimolar (mM) TCEP , 10 millimolar (mM) IAA , and 2 µL Trypsin (1 mg/ml) (1:50 trypsin:protein ratio). Adjust as needed for your data acquisition protocols.
add 41.67 µL protein (2.4 ug/ul)
add 2.5 µL TCEP (100 mM)
add 2.5 µL IAA (200mM)
add 2 µL Trypsin (1 mg/ml)
add 1.33 µL AMBIC
up to 50 µL total volume
Note
If you do not have enough protein, you can set your final protein concentration to 1 ug/ul.
add 20.83 µL protein (2.4 ug/ul)
add 2.5 µL TCEP (100 mM)
add 2.5 µL IAA (200 mM)
add 1 µL Trypsin (1 mg/ml)
add 23.17 µL AMBIC
up to 50 µL total volume
Incubate at 37 °C for 04:00:00 -16:00:00 .
4h
Centrifuge at 4000 rpm, 4°C, 00:15:00 .
Carefully pipet out clear liquid sample into plastic autosampler vials (ThermoFisherScientific, Cat.#03-060-016) or a 96-well plate (BIO-RAD, Cat.#HSP9601).
Store at -20 °C until ready for LC-MS/MS analysis.