| Literature DB >> 34413958 |
Jonathan D Mortison1, Ivan Cornella-Taracido1, Gireedhar Venkatchalam2, Anthony W Partridge2, Nirodhini Siriwardana1, Simon M Bushell1.
Abstract
Determination of target engagement for candidate drug molecules in the native cellular environment is a significant challenge for drug discovery programs. The cellular thermal shift assay (CETSA) has emerged as a powerful tool for determining compound target engagement through measurement of changes to a protein's thermal stability upon ligand binding. Here, we present a HiBiT thermal shift assay (BiTSA) that deploys a quantitative peptide tag for determination of compound target engagement in the native cellular environment using a high throughput, plate-based luminescence readout. We demonstrate that BiTSA can rapidly assess cellular target engagement of small molecule ligands against their cognate targets and highlight two applications of BiTSA for differentiating small molecules targeting mutant KRAS and TP53.Entities:
Year: 2021 PMID: 34413958 PMCID: PMC8366000 DOI: 10.1021/acsmedchemlett.1c00276
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.632