Method Article

Using High Content Imaging to Quantify Target Engagement in Adherent Cells

DOI:

10.3791/58670

November 29th, 2018

In This Article

Summary

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Measurements of drug target engagement are central to effective drug development and chemical probe validation. Here, we detail a protocol for measuring drug-target engagement using high content imaging in a microplate-compatible adaption of the cellular thermal shift assay (CETSA).

Abstract

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Quantitating the interaction of small molecules with their intended protein target is critical for drug development, target validation and chemical probe validation. Methods that measure this phenomenon without modification of the protein target or small molecule are particularly valuable though technically challenging. The cellular thermal shift assay (CETSA) is one technique to monitor target engagement in living cells. Here, we describe an adaptation of the original CETSA protocol, which allows for high throughput measurements while retaining subcellular localization at the single cell level. We believe this protocol offers important advances to the application of CETSA for in-depth characterization of compound-target interaction, especially in heterogeneous populations of cells.

Introduction

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When developing new drugs or chemical probes it is essential to couple the observed pharmacological effect or functional readout to measurements of target occupancy or engagement in live cells1,2,3. These data are necessary both to ensure that the small molecule in fact reaches its desired target and to validate the biological hypothesis behind protein target selection4,5. Furthermore, during drug development, model systems of increasing complexity are used to select and corroborate a lead compound prior to clinical t....

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Protocol

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1. Seeding of Cells

NOTE: For a general overview of the workflow see Figure 1. A detailed list of materials and reagents are available in the Table of Materials.

  1. Prior to seeding of the cells, drill holes with a standard drill in the frame of black 384-well imaging assay plates to avoid air bubbles being trapped under the plate later during the heating step. To avoid plastic particles entering the wells during this step and to maintain sterile conditions, seal the plates with an adhesive aluminum foil or cover the plate prior to drilling in a tissue culture hood. Ty....

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Results

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The protocol outlined in Figure 1 describes the basic workflow for running CETSA assays on adherent cells with detection of remaining soluble protein by high content imaging. This workflow can be easily adapted to all stages of assay development by modifying the plate layout of the compounds or reagents14. We detail expected results for several anticipated use cases below.

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Discussion

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As discussed in the results section, there are several key steps to the procedure. First, it is important to identify a high-quality affinity reagent. We recommend screening a small library of antibodies for each desired target. After a primary antibody has been selected, it is also important to validate the system for a number of different binding sites of the protein target if appropriate. Counter-screening for compounds that interfere with the assay signal as shown in Figure 2C by omittin.......

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Disclosures

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The authors have no disclosures to report.

Acknowledgements

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The authors acknowledge infrastructure support from Science for Life Laboratory and Karolinska Institutet. The authors also acknowledge input and discussions with Michaela Vallin, Magdalena Otrocka and Thomas Lundbäck.

....

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Phosphate-buffered saline (PBS)Medicago09-9400-100
TrypLE ExpressThermoFisher Scientific12604013for detaching cells and subculturing
16% paraformaldehyde (PFA)ThermoFisher Scientific28908fixative
Goat anti-rabbit IgG (H+L), Alexa Fluor 488 conjugated antibodyThermoFisher ScientificA11008secondary antibody
HCS CellMask Red stainThermoFisher ScientificH32712Cytoplasm stain
NP-40Sigma-Aldrich56741for permeabilization
Hoechst stain 33342Sigma-AldrichB2261nuclear stain
Dulbecco’s modified Eagle’s medium (DMEM) - high GlucoseSigma-Aldrich6429cell culture media component
Heat-inactivated fetal bovine serum (FBS)Sigma-AldrichF9665cell culture media component
Penicillin-StreptomycinSigma-AldrichP4333cell culture media component
Corning, breathable plate sealSigma-AldrichCLS3345for copound incubation step
Rabbit anti-p38 antibody [E229]Abcamab170099primary antibody, LOT:GR305364-16
Falcon, Black 384-well clear bottom imaging platesVWR736-2044imaging plates
Greiner, 384-well low volume polypropylene platesVWR784201
Adhesive aluminum foilVWR30127790
Peelable aluminium sealAgilent24210-001for PlateLoc
LY2228820SelleckchemS1494p38α inhibitor
PH797804SelleckchemPH797804p38α inhibitor
BIRB796SelleckchemS1574p38α inhibitor
SB203580Tocris1202p38α inhibitor
AMG 548Tocris3920p38α inhibitor
RWJ 67657Tocris2999p38α inhibitor
L-SkepinoneCBCS compound collectionp38α inhibitor
Bovine serum albumin (BSA)Sigma-AldrichA7030blocking agent
SDS (sodium dodecyl sulfate)BDH44244used in antigen retrieval
GlycineSigma-AldrichG8898used in antigen retrieval
A-431 cellsATCCATC-CRL-1555
Echo 550LabcyteFor preparation of compound plates
Plate sealerAgilentPlateLoc
Bulk reagent dispenserThermo Scientific5840300Multidrop Combi
Automated liquid handlingAgilentBravo liquid handling platform; used for compound plate preparation
Plate washerTecanHydrospeed
Water bathJulaboTW12
ThermocoupleVWRThermocouple traceable lab thermometer
High content imagerMolecular DevicesImageXpress Micro XLS Widefield High-Content Analysis System

References

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  1. Morgan, P., et al. Impact of a five-dimensional framework on R&D productivity at AstraZeneca. Nature Reviews Drug Discovery. 17 (3), 167-181 (2018).
  2. Freedman, L. P., Cockburn, I. M., Simcoe, T. S. The Economics of Reproducibility in Preclinical Research. <....

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Tags

Cellular Thermal Shift AssayCompound Target InteractionSubcellular LocalizationIsothermal Dose ResponseThermal Aggregation CurveAntibody RecognitionPlate Washer

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