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An analytical workflow based on liquid chromatography, trapped ion mobility spectrometry, and time-of-flight mass spectrometry (LC-TIMS-ToF MS/MS) for high confidence and highly reproducible "bottom-up" analysis of histone modifications and identification based on principal parameters (retention time [RT], collision cross section [CCS], and accurate mass-to-charge [m/z] ratio).
Histone proteins are highly abundant and conserved among eukaryotes and play a large role in gene regulation as a result of structures known as posttranslational modifications (PTMs). Identifying the position and nature of each PTM or pattern of PTMs in reference to external or genetic factors allows this information to be statistically correlated with biological responses such as DNA transcription, replication, or repair. In the present work, a high-throughput analytical protocol for the detection of histone PTMs from biological samples is described. The use of complementary liquid chromatography, trapped ion mobility spectrometry, and time-of-flight mass spectrometry (LC-TIMS-ToF MS/MS) enables the separation and PTM assignment of the most biologically relevant modifications in a single analysis. The described approach takes advantage of recent developments in dependent data acquisition (DDA) using parallel accumulation in the mobility trap, followed by sequential fragmentation and collision-induced dissociation. Histone PTMs are confidently assigned based on their retention time, mobility, and fragmentation pattern.
In eukaryotic cells, DNA is packaged as chromatin into functional units called nucleosomes. These units are composed of an octamer of four core histones (two each of H2A, H2B, H3, and H4)1,2,3,4. Histones are amongst the most abundant and highly conserved proteins in eukaryotes, which are largely responsible for gene regulation5. Histone posttranslational modifications (PTMs) play a large role in the regulation of chromatin dynamics and rigger various biological processes such as DNA transcription, replication, and re....
NOTE: Histone samples were extracted using a method adapted from Bhanu et al. (2020)12.
1. Sample preparation
A bottom-up proteomic workflow (Figure 7) typically involves the following: extraction of the target protein(s) from a crude sample, followed by quantifying the concentration of the protein(s), and then fractionation, usually by gel electrophoresis or liquid chromatography. After fractionation, the proteins are digested using a proteolytic enzyme (often trypsin), and finally, mass spectrometric analysis of the resulting peptides and protein identification using an established database
Histones are basic proteins that regulate chromatin structure by interacting with DNA in the form of octamers consisting of the four core histones (two each of H2A, H2B, H3, and H4)20. Histones contain numerous lysine and arginine residues, which are readily modified, leading to extensive PTMs that alter the chromatin chemistry by influencing histone function or by binding to other cellular proteins21. PTMs can elicit biological responses by working in tandem, with specific.......
This material is based upon work supported by the National Science Foundation under Grant No. HRD-1547798 and Grant No. HRD-2111661. These NSF Grants were awarded to Florida International University as part of the Centers of Research Excellence in Science and Technology (CREST) Program. This is contribution number 1672 from the Institute of Environment, a Preeminent Program at Florida International University. Additional support was provided by the National Institute of Health under Grant No. R21AI135469 to Francisco Fernandez-Lima and Grant No. R01HD106051 to Benjamin A. Garcia, as well as by the National Science Foundation under Grant No. CHE-2127882 to Benjamin A. ....
Name | Company | Catalog Number | Comments |
-80 °C Freezer | |||
1x Phosphate Buffered Saline (PBS), pH 7.4 | Thermo Fisher Scientific | 10010023 | Animal Origin-Free |
1 mL Pipette Tips | Thermo Fisher Scientific | 94060710 | Finntip Flex 1000 μL, nonsterile, nonfiltered, racked tips |
1.5 mL Microcentrifuge Tubes | Thermo Fisher Scientific | 14-282-300 | Use these tubes for the simple and safe processing of sample volumes up to 1.5 mL |
10 µL Pipette Tips | Thermo Fisher Scientific | 94060100 | Finntip Flex, 10 μL, nonsterile, non-filtered, racked |
10% NP-40 | Thermo Fisher Scientific | 28324 | NP-40 Surfact-Amps Detergent Solution |
10x Dulbecco’s PBS without Ca2+/Mg2+ | (Mediatech) | MT21031CM | |
15 mL Conical Tubes | Corning | 352196 | Falcon Conical Centrifuge Tubes |
200 µL Gel-Loading Pipette Tips | Thermo Fisher Scientific | 02-707-138 | Fisherbrand Gel-Loading Tips, 1–200 μL |
200 µL Pipette Tips | Thermo Fisher Scientific | 94060310 | Finntip Flex 200μL, nonsterile, nonfiltered, racked tips |
2x Laemmli Sample Buffer | Bio-Rad | 1610737 | Premixed protein sample buffer for SDS-PAGE |
50 mL Conical Tubes | Corning | 352070 | Falcon Conical Centrifuge Tubes |
96-well flat bottom plate | Thermo Fisher Scientific | 12565501 | |
96-well plate, V-Bottom 600 μL | Axygen | P-DW-500-C-S | |
Acetone | Sigma Aldrich | 179124 | ACS reagent, ≥99.5% |
Acetonitrile (ACN) | Thermo Fisher Scientific | A998 | HPLC, Fisher Chemical |
Acetonitrile with 0.1% Formic acid (v/v), LC/MS Grade | Thermo Fisher Scientific | LS120 | Optima LC/MS Grade, Thermo Scientific |
AEBSF | Thermo Fisher Scientific | 328110500 | AEBSF hydrochloride, 98% |
Ammonium bicarbonate, NH4HCO3 | Sigma Aldrich | 09830 | BioUltra, ≥99.5% (T) |
Ammonium hydroxide solution, NH4OH | Sigma Aldrich | AX1303 | Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS |
Argon (Ar) | Airgas | AR HP 300 | |
BEH C18 HPLC column | Waters | 186003625 | XBridge Peptide BEH C18 Column, 300 Å, 5 µm, 4.6 mm X 250 mm, 1K–15K |
Bovine Serum Albumin (BSA) | Sigma Aldrich | A7906 | Heat shock fraction, pH 7, ≥98% |
Calcium chloride, CaCl2 | Sigma Aldrich | C4901 | Anhydrous, powder, ≥97% |
Cell dissociation buffer | Thermo Fisher Scientific | 13151014 | |
Ceramic scoring wafer | Restek | 20116 | |
Compass DataAnalysis 6.0 | Bruker Datonics | ||
Compass HyStar 6.2 | Bruker Daltonics | ||
Compass IsotopePattern | Bruker Daltonics | ||
Compass timsControl 4.1 | Bruker Daltonics | ||
Coomassie Brilliant Blue R-250 | Bio-Rad | 1610436 | |
Deep Well, 96-Well Microplate, 2.0 mL | Thermo Fisher Scientific | 89237526 | |
Disposable Cell Lifters | Thermo Fisher Scientific | Â 08100240 | Fisherbrand Cell Lifters; Disposable lifters quickly remove cell layers |
Disposable Pellet Pestles | Thermo Fisher Scientific | 12-141-363 | Fisherbrand Pellet Pestles; Resuspend protein and DNA pellets or grind soft tissue in microcentrifuge tubes |
Dithiothreitol (DTT) | Thermo Fisher Scientific | P2325 | 1 M |
Formic acid (FA) | Sigma Aldrich | 695076 | ACS reagent, ≥96% |
Fused silica capillary 75 μm ID x 363 μm OD | (Molex (Polymicro) | TSP075375 | |
Glacial Acetic Acid | Thermo Fisher Scientific | A38S | Acetic Acid, Glacial (Certified ACS), Fisher Chemical |
Glass Pasteur Pipettes | Sigma Aldrich | BR747725-1000EA | |
High-Performance Liquid Chromatograph | Â Shimadzu | Shimadzu Prominence 20 HPLC UFLC System | |
Hydrochloric acid, HCl | Sigma Aldrich | 258148 | ACS reagent, 37% |
Hypercarb 30-40 μm Carbon 150–300 Å | Thermo Fisher Scientific | 60106-402 | |
Hypersep cartridge | Thermo Fisher Scientific | 60109-404 | |
LC/MS Calibration Standard, for ESI-ToF | Agilent | G1969-85000 | TuningMix |
Magnesium chloride, MgCl2 | Sigma Aldrich | M8266 | Anhydrous, ≥98% |
Methanol, for HPLC | Thermo Fisher Scientific | A454 | Optima for HPLC, Fisher Chemical  |
Microcentrifuge Tube Adapters | GL Sciences | 501021514 | |
Microcystin | Thermo Fisher Scientific | 50-200-8727 | Enzo Life Sciences Microcystin-LA |
MS sample vial, LaPhaPack, Snap, 12 mm x 32 mm | LEAP PAL Parts | LAP.11190933 | |
Nanodrop | Thermo Fisher Scientific | model: ND3300 | |
Nitrogen (N2) | Airgas | NI UHP300 | |
PEAKS Studio X+ | Bioinformatic Solutions | ||
pH indicator strips, Instachek | Micro Essential Lab | JR-113 | Model: Hydrion |
Potassium chloride, KCl | Sigma Aldrich | P3911 | ACS reagent, 99.0%–100.5% |
Pressure Injection Cell | Next Advance | Â model: PC77 | |
Propionic Anhydride | Sigma Aldrich | 8.00608 | For synthesis |
Refrigerated Centrifuge (700–18,000 x g) | NuAire, model: Nuwind | NU-C200V | |
Reprosil-Pur 120 C18-AQ 3 μm, 3 g | ESI Source Solutions | r13.aq.0003 | |
SDS-PAGE Gels | Bio-Rad | 4569035 | Any kD precast polyacrylamide gel, 8.6 cm × 6.7 cm (W × L), for use with Mini-PROTEAN Electrophoresis Cells |
Sodium butyrate | Thermo Fisher Scientific | A11079.06 | 98+% |
Sodium chloride, NaCl | Sigma Aldrich | S9888 | ACS reagent, ≥99.0% |
SPE disk, C18 | VWR | 76333-134 | Empore SPE disk, C18, CDS Analytical, 90 mm x 0.5 mm, 12 µm |
SpeedVac+ vacuum pump and plate rotor | Savant | model: SC210A | |
Sucrose | Millipore | 1.07651 | suitable for microbiology |
Sulfuric acid, H2SO4Â | Sigma Aldrich | 339741 | 99.999% |
TIMS-ToF Mass Spectrometer | Bruker Daltonics | model Tims tof ms | |
Trichloroacetic acid solution, TCA | Sigma Aldrich | T0699 | 6.1Â N |
Trifluoroacetic acid (TFA) | Sigma Aldrich | 302031 | Suitable for HPLC, ≥99.0% |
Triversa Nanomate | Advion | model: TR263 | |
TrypsinProtease, MS Grade | Thermo Fisher Scientific | 90057 | |
Tube rotator | Thermo Fisher Scientific | 88881001 | |
Vortex Mixer | Thermo Fisher Scientific | 88880017 | |
Water with 0.1% Formic acid (v/v), LC/MS Grade | Thermo Fisher Scientific | LS118 | Optima LC/MS Grade, Thermo Scientific |
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