Molecular Chaperones Hsp90 and Hsp70 Deliver Preproteins to the Mitochondrial Import Receptor Tom70

TLDR

The role of cytosolic factors in protein targeting to mitochondria is poorly understood. The study proposes a novel mechanism whereby chaperones are recruited by the mitochondrial outer membrane receptor Tom70 for specific preprotein targeting. In mammals, Hsp90 and Hsp70 dock onto a TPR domain of Tom70, delivering preproteins for translocation that requires Hsp90 ATPase activity, while in yeast Hsp70 performs this role. Disrupting chaperone–Tom70 interaction blocks preprotein import, and Hsp70 docking is essential for forming a productive preprotein/Tom70 complex.

Abstract

The role of cytosolic factors in protein targeting to mitochondria is poorly understood. Here, we show that in mammals, the cytosolic chaperones Hsp90 and Hsp70 dock onto a specialized TPR domain in the import receptor Tom70 at the outer mitochondrial membrane. This interaction serves to deliver a set of preproteins to the receptor for subsequent membrane translocation dependent on the Hsp90 ATPase. Disruption of the chaperone/Tom70 recognition inhibits the import of these preproteins into mitochondria. In yeast, Hsp70 rather than Hsp90 is used in import, and Hsp70 docking is required for the formation of a productive preprotein/Tom70 complex. We outline a novel mechanism in which chaperones are recruited for a specific targeting event by a membrane-bound receptor.