Fe-S Cluster Hsp70 Chaperones: The ATPase Cycle and Protein Interactions.

Abstract:

:Hsp70 chaperones and their obligatory J-protein cochaperones function together in many cellular processes. Via cycles of binding to short stretches of exposed amino acids on substrate proteins, Hsp70/J-protein chaperones not only facilitate protein folding but also drive intracellular protein transport, biogenesis of cellular structures, and disassembly of protein complexes. The biogenesis of iron-sulfur (Fe-S) clusters is one of the critical cellular processes that require Hsp70/J-protein action. Fe-S clusters are ubiquitous cofactors critical for activity of proteins performing diverse functions in, for example, metabolism, RNA/DNA transactions, and environmental sensing. This biogenesis process can be divided into two sequential steps: first, the assembly of an Fe-S cluster on a conserved scaffold protein, and second, the transfer of the cluster from the scaffold to a recipient protein. The second step involves Hsp70/J-protein chaperones. Via binding to the scaffold, chaperones enable cluster transfer to recipient proteins. In eukaryotic cells mitochondria have a key role in Fe-S cluster biogenesis. In this review, we focus on methods that enabled us to dissect protein interactions critical for the function of Hsp70/J-protein chaperones in the mitochondrial process of Fe-S cluster biogenesis in the yeast Saccharomyces cerevisiae.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Dutkiewicz R,Nowak M,Craig EA,Marszalek J

doi

10.1016/bs.mie.2017.07.004

subject

Has Abstract

pub_date

2017-01-01 00:00:00

pages

161-184

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(17)30234-3

journal_volume

595

pub_type

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