Cytosolic Hsp70 and Hsp40 chaperones enable the biogenesis of mitochondrial ?-barrel proteins.

Mitochondrial ?-barrel proteins are encoded in the nucleus, translated by cytosolic ribosomes, and then imported into the organelle. Recently, a detailed understanding of the intramitochondrial import pathway of ?-barrel proteins was obtained. In contrast, it is still completely unclear how newly synthesized ?-barrel proteins reach the mitochondrial surface in an ...
import-competent conformation. In this study, we show that cytosolic Hsp70 chaperones and their Hsp40 cochaperones Ydj1 and Sis1 interact with newly synthesized ?-barrel proteins. These interactions are highly relevant for proper biogenesis, as inhibiting the activity of the cytosolic Hsp70, preventing its docking to the mitochondrial receptor Tom70, or depleting both Ydj1 and Sis1 resulted in a significant reduction in the import of such substrates into mitochondria. Further experiments demonstrate that the interactions between ?-barrel proteins and Hsp70 chaperones and their importance are conserved also in mammalian cells. Collectively, this study outlines a novel mechanism in the early events of the biogenesis of mitochondrial outer membrane ?-barrel proteins.
Mesh Terms:
Cells, Cultured, HSP40 Heat-Shock Proteins, HSP70 Heat-Shock Proteins, Humans, Mitochondria, Mitochondrial Membrane Transport Proteins, Mitochondrial Precursor Protein Import Complex Proteins, Protein Binding, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
J Cell Biol
Date: Sep. 03, 2018
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