| Literature DB >> 35063133 |
Maximilian M Biebl1, Florent Delhommel2, Ofrah Faust3, Krzysztof M Zak4, Ganesh Agam5, Xiaoyan Guo6, Moritz Mühlhofer1, Vinay Dahiya1, Daniela Hillebrand1, Grzegorz M Popowicz4, Martin Kampmann6, Don C Lamb5, Rina Rosenzweig3, Michael Sattler7, Johannes Buchner8.
Abstract
In the eukaryotic cytosol, the Hsp70 and the Hsp90 chaperone machines work in tandem with the maturation of a diverse array of client proteins. The transfer of nonnative clients between these systems is essential to the chaperoning process, but how it is regulated is still not clear. We discovered that NudC is an essential transfer factor with an unprecedented mode of action: NudC interacts with Hsp40 in Hsp40-Hsp70-client complexes and displaces Hsp70. Then, the interaction of NudC with Hsp90 allows the direct transfer of Hsp40-bound clients to Hsp90 for further processing. Consistent with this mechanism, NudC increases client activation in vitro as well as in cells and is essential for cellular viability. Together, our results show the complexity of the cooperation between the major chaperone machineries in the eukaryotic cytosol.Entities:
Keywords: Glucocorticoid receptor; Hsp40; Hsp70; Hsp90; NMR spectroscopy; NudC; co-chaperones; molecular chaperones; protein folding; spFRET
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Year: 2022 PMID: 35063133 DOI: 10.1016/j.molcel.2021.12.031
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970