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• W2989386735 abstract "Abstract The interaction between the C-terminal transactivation domain of HIF-1α (CTAD-HIF-1α) and the transcriptional adapter zinc binding 1 (TAZ1) domain of CREB binding protein participate in the initiation of gene transcription during hypoxia. Unbound CTAD-HIF-1α is disordered but undergoes a disorder-to-order transition upon binding to TAZ1. We have here performed NMR side chain and backbone relaxation studies on TAZ1 and side chain relaxation measurements on CTAD-HIF-1α in order to investigate the role of picosecond to nanosecond dynamics. We find that the internal motions are significantly affected upon binding, both on the side chain and the backbone level. The dynamic response corresponds to a conformational entropy change that contributes substantially to the binding thermodynamics for both binding partners. Furthermore, the conformational entropy change for the well-folded TAZ1 varies upon binding to different IDP targets. We further identify a cluster consisting of side chains in bound TAZ1 and CTAD-HIF-1α that experience extensive dynamics and are part of the binding region that involves the N-terminal end of the LPQL motif in CTAD-HIF-1α; a feature that might have an important role in the termination of the hypoxic response." @default.
• W2989386735 created "2019-11-22" @default.
• W2989386735 creator A5037925267 @default.
• W2989386735 creator A5049224704 @default.
• W2989386735 date "2019-11-12" @default.
• W2989386735 modified "2023-10-13" @default.
• W2989386735 title "Characterization of the dynamics and the conformational entropy in the binding between TAZ1 and CTAD-HIF-1α" @default.
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• W2989386735 doi "https://doi.org/10.1038/s41598-019-53067-8" @default.
• W2989386735 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6851107" @default.
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• W2989386735 hasPublicationYear "2019" @default.
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