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Method Article

Simultaneous Measurement of HDAC1 and HDAC6 Activity in HeLa Cells Using UHPLC-MS

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DOI:

10.3791/55878

August 10th, 2017

* These authors contributed equally

In This Article

Summary

The present method serves to identify isoform-specific inhibitors of histone deacetylases (HDAC) in HeLa cells by the UHPLC-MS analysis of multiple substrates. This is an antibody-free method developed to reflect HDAC1 and HDAC6 activity in the living cell environment, in contrast to single-isoform cell-free assays.

Abstract

The search for new histone deacetylase (HDAC) inhibitors is of increasing interest in drug discovery. Isoform selectivity has been in the spotlight since the approval of romidepsin, a class I HDAC inhibitor for cancer therapy, and the clinical investigation of HDAC6-specific inhibitors for multiple myeloma. The present method is used to determine the inhibitory activity of test compounds on HDAC1 and HDAC6 in cells. The isoform activity is measured using the ultra-high-performance liquid chromatography – mass spectrometry (UHPLC-MS) analysis of specific substrates incubated with treated and untreated HeLa cells. The method has the advantage of reflecting the endogenous HDAC activity within the cell environment, in contrast to cell-free biochemical assays conducted on isolated isoforms. Moreover, because it is based on the quantification of synthetic substrates, the method does not require the antibody recognition of endogenous acetylated proteins. It is easily adaptable to several cell lines and an automated process. The method has already proved useful in finding HDAC6-selective compounds in neuroblasts. Representative results are shown here with the standard HDAC inhibitors trichostatin A (non-specific), MS275 (HDAC1-specific), and tubastatin A (HDAC6-specific) using HeLa cells.

Introduction

HDACs belong to a family of enzymes able to deacetylate histones within the chromatin structure. They also have other protein substrates in the cytosol and are located in various cell compartments. A total of 18 HDAC isoforms have been identified so far and have been related to several cell mechanisms, including the regulation of transcription factors and gene expression, as well as cell signaling and transport1,2,3,4,5,6,7. HDAC catalyti....

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Protocol

1. Cell Culture

NOTE: The following steps are performed in a standard tissue culture hood. Familiarity with sterile technique is expected.

  1. Culture HeLa cells to 80% confluency in a T75 cell culture flask in MEM supplemented with 10% fetal bovine serum, penicillin G (100 U/mL), and streptomycin (100 mg/mL).
    NOTE: Cell culture, treatment, and lysis steps are conducted under laminar flow, with cell incubation steps at 37 °C performed in a humidified atmosphere of 5% CO2 under sterile conditions.
  2. Wash the cells twice with 5 mL of DPBS, aspirate the DPBS, and add 1 mL of cell dissociation reagent. Incubate a....

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Results

To demonstrate the application of the method to identifying non-selective and selective inhibitors for HDAC1 (class I) and HDAC6 (class IIb), HeLa cells were treated with known standard compounds: trichostatin A (non-selective between HDAC1 and HDAC6)18, MS275 (HDAC1-selective inhibitor)19, and tubastatin A (HDAC6-selective inhibitor)20. By using the present method (Figure 1), IC50

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Discussion

HDAC inhibition is a hot topic in drug discovery, with a current focus on HDAC6-selective inhibitors for cancer therapy21. HDAC selectivity is usually assessed by a series of high-throughput, cell-free assays, which intend to determine the inhibitory potency towards individual HDAC isoforms21. However, the selectivity of an inhibitor must be additionally confirmed in living cells by evaluating the acetylation status of endogenous protein substrates, such as histones (for cl.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors acknowledge COST Action CM1406 (Epigenetic Chemical Biology). Research reported in this publication was supported by the Pierre Mercier foundation.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
BATCPSigma-AldrichB4061
MALSigma-AldrichSCP0168Synonym: BOC-Ac-Lys-AMC
MOCPACSigma-AldrichM2195
MS275Sigma-AldrichEPS002
Trichostatin ASigma-AldrichT8552
Tubastatin ASigma-AldrichSML0044
Acetonitrile, HPLC gradeFisher Scientific10660131
Formic acid, LC/MS gradeFisher Scientific10596814
H2O, HPLC gradedistilled H2O filtered through a Milli-Q purification system
HeLa cellsATCCATCC CRM-CCL-2
Cell dissociation reagent TrypLE ExpressThermoFisher Scientific12604013
DMSO, cell culture gradeApplichem146463
DPBSThermoFisher Scientific14190144
Fetal bovine serumBiowestS1810
MEMThermoFisher Scientific22561021
Penicillin-StreptomycinBioconcept4-01F00-H
10x RIPA bufferAbcamab156034
SigmaFast protease inhibitor tabletsSigma-AldrichS8820
96-well plates, sterile, flat-bottom, tissue culture treated CorningVWR29442-058
96-well plates, non-sterile, V-bottom CorningVWR29442-404used in the centrifugation step
96-well plate, conical bottom, NuncThermoFisher Scientific249944compatible with the Acquity UHPLC system
T75 cell culture flasks CorningSigma-AldrichCLS430641
Peelable heat sealing foilWaters186002789
Acquity UPLC systemWaters
Eppendorf Centrifuge 5810 RFisher Scientific05-413-323
Integration software: MassLynx V4.1WatersCatalog number not available
Combi thermo-sealer SP-0669/240WatersCatalog number not available
Quattro micro API Tandem Quadrupole SystemWatersCatalog number not available

References

  1. Arrowsmith, C. H., Bountra, C., Fish, P. V., Lee, K., Schapira, M. Epigenetic protein families: a new frontier for drug discovery. Nat Rev Drug Discov. 11 (5), 384-400 (2012).
  2. Henikoff, S., Greally, J. M. Epigenetics, cellular memory and gene regulation. Curr Biol. 26 ....

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Tags

HDAC1 HDAC6 ActivityUHPLC MS AnalysisHDAC Inhibitor SelectivitySubstrate Deacetylation AssayCell Lysis ProtocolTrichostatin A MS275Tubastatin A SpecificityMOCPAC BATCP DetectionDrug Discovery Screening