<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(10)</volume><submitter>Lenz T</submitter><pubmed_abstract>Chemical biology and the application of small molecules has proven to be a potent perturbation strategy, especially for the functional elucidation of proteins, their networks, and regulators. In recent years, the cellular thermal shift assay (CETSA) and its proteome-wide extension, thermal proteome profiling (TPP), have proven to be effective tools for identifying interactions of small molecules with their target proteins, as well as off-targets in living cells. Here, we asked the question whether isothermal dose-response (ITDR) CETSA can be exploited to characterize secondary effects downstream of the primary binding event, such as changes in post-translational modifications or protein-protein interactions (PPI). By applying ITDR-CETSA to MAPK14 kinase inhibitor treatment of living HL-60 </pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>5605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9147192</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;u>S&lt;/u>mall &lt;u>M&lt;/u>olecule &lt;u>Ar&lt;/u>ranged &lt;u>T&lt;/u>hermal &lt;u>P&lt;/u>roximity &lt;u>C&lt;/u>o&lt;u>a&lt;/u>ggregation (smarTPCA)-A Novel Approach to Characterize Protein-Protein Interactions in Living Cells by Similar Isothermal Dose-Responses.</pubmed_title><pmcid>PMC9147192</pmcid><pubmed_authors>Lenz T</pubmed_authors><pubmed_authors>Stuhler K</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;u>S&lt;/u>mall &lt;u>M&lt;/u>olecule &lt;u>Ar&lt;/u>ranged &lt;u>T&lt;/u>hermal &lt;u>P&lt;/u>roximity &lt;u>C&lt;/u>o&lt;u>a&lt;/u>ggregation (smarTPCA)-A Novel Approach to Characterize Protein-Protein Interactions in Living Cells by Similar Isothermal Dose-Responses.</name><description>Chemical biology and the application of small molecules has proven to be a potent perturbation strategy, especially for the functional elucidation of proteins, their networks, and regulators. In recent years, the cellular thermal shift assay (CETSA) and its proteome-wide extension, thermal proteome profiling (TPP), have proven to be effective tools for identifying interactions of small molecules with their target proteins, as well as off-targets in living cells. Here, we asked the question whether isothermal dose-response (ITDR) CETSA can be exploited to characterize secondary effects downstream of the primary binding event, such as changes in post-translational modifications or protein-protein interactions (PPI). By applying ITDR-CETSA to MAPK14 kinase inhibitor treatment of living HL-60 </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-04-08T09:42:05.026Z</modification><creation>2024-11-06T15:41:56.301Z</creation></dates><accession>S-EPMC9147192</accession><cross_references><pubmed>35628420</pubmed><doi>10.3390/ijms23105605</doi></cross_references></HashMap>