Literature DB >> 23828940

Monitoring drug target engagement in cells and tissues using the cellular thermal shift assay.

Daniel Martinez Molina1, Rozbeh Jafari, Marina Ignatushchenko, Takahiro Seki, E Andreas Larsson, Chen Dan, Lekshmy Sreekumar, Yihai Cao, Pär Nordlund.   

Abstract

The efficacy of therapeutics is dependent on a drug binding to its cognate target. Optimization of target engagement by drugs in cells is often challenging, because drug binding cannot be monitored inside cells. We have developed a method for evaluating drug binding to target proteins in cells and tissue samples. This cellular thermal shift assay (CETSA) is based on the biophysical principle of ligand-induced thermal stabilization of target proteins. Using this assay, we validated drug binding for a set of important clinical targets and monitored processes of drug transport and activation, off-target effects and drug resistance in cancer cell lines, as well as drug distribution in tissues. CETSA is likely to become a valuable tool for the validation and optimization of drug target engagement.

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Year:  2013        PMID: 23828940     DOI: 10.1126/science.1233606

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  473 in total

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Journal:  Nat Protoc       Date:  2015-09-17       Impact factor: 13.491

2.  Thermal proteome profiling monitors ligand interactions with cellular membrane proteins.

Authors:  Friedrich B M Reinhard; Dirk Eberhard; Thilo Werner; Holger Franken; Dorothee Childs; Carola Doce; Maria Fälth Savitski; Wolfgang Huber; Marcus Bantscheff; Mikhail M Savitski; Gerard Drewes
Journal:  Nat Methods       Date:  2015-11-02       Impact factor: 28.547

3.  A cell-penetrant lactam-stapled peptide for targeting eIF4E protein-protein interactions.

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Journal:  Eur J Med Chem       Date:  2020-07-25       Impact factor: 6.514

4.  Development of SKI-349, a dual-targeted inhibitor of sphingosine kinase and microtubule polymerization.

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5.  MAST1 Drives Cisplatin Resistance in Human Cancers by Rewiring cRaf-Independent MEK Activation.

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Journal:  Cancer Cell       Date:  2018-07-19       Impact factor: 31.743

6.  Protein mimetic amyloid inhibitor potently abrogates cancer-associated mutant p53 aggregation and restores tumor suppressor function.

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Journal:  Nat Commun       Date:  2021-06-25       Impact factor: 14.919

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Journal:  FASEB J       Date:  2020-02-17       Impact factor: 5.191

8.  Codon usage regulates human KRAS expression at both transcriptional and translational levels.

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Journal:  J Biol Chem       Date:  2018-10-01       Impact factor: 5.157

9.  A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models.

Authors:  Elayne Chan-Penebre; Kristy G Kuplast; Christina R Majer; P Ann Boriack-Sjodin; Tim J Wigle; L Danielle Johnston; Nathalie Rioux; Michael J Munchhof; Lei Jin; Suzanne L Jacques; Kip A West; Trupti Lingaraj; Kimberly Stickland; Scott A Ribich; Alejandra Raimondi; Margaret Porter Scott; Nigel J Waters; Roy M Pollock; Jesse J Smith; Olena Barbash; Melissa Pappalardi; Thau F Ho; Kelvin Nurse; Khyati P Oza; Kathleen T Gallagher; Ryan Kruger; Mikel P Moyer; Robert A Copeland; Richard Chesworth; Kenneth W Duncan
Journal:  Nat Chem Biol       Date:  2015-04-27       Impact factor: 15.040

10.  Piperidinyl Ureas Chemically Control Defective in Cullin Neddylation 1 (DCN1)-Mediated Cullin Neddylation.

Authors:  Jared T Hammill; Daniel C Scott; Jaeki Min; Michele C Connelly; Gloria Holbrook; Fangyi Zhu; Amy Matheny; Lei Yang; Bhuvanesh Singh; Brenda A Schulman; R Kiplin Guy
Journal:  J Med Chem       Date:  2018-03-26       Impact factor: 7.446

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