Mechanism of Hsp70 specialized interactions in protein translocation and the unfolded protein response

Open Biol. 2020 Aug;10(8):200089. doi: 10.1098/rsob.200089. Epub 2020 Aug 19.

Abstract

Hsp70 chaperones interact with substrate proteins in a coordinated fashion that is regulated by nucleotides and enhanced by assisting cochaperones. There are numerous homologues and isoforms of Hsp70 that participate in a wide variety of cellular functions. This diversity can facilitate adaption or specialization based on particular biological activity and location within the cell. In this review, we highlight two specialized binding partner proteins, Tim44 and IRE1, that interact with Hsp70 at the membrane in order to serve their respective roles in protein translocation and unfolded protein response signalling. Recent mechanistic data suggest analogy in the way the two Hsp70 homologues (BiP and mtHsp70) can bind and release from IRE1 and Tim44 upon substrate engagement. These shared mechanistic features may underlie how Hsp70 interacts with specialized binding partners and may extend our understanding of the mechanistic repertoire that Hsp70 chaperones possess.

Keywords: BiP; Hsp70 chaperones; IRE1; Tim44; UPR; protein translocation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Carrier Proteins
  • Cell Membrane / metabolism
  • Endoplasmic Reticulum / metabolism
  • Gene Expression Regulation*
  • HSP70 Heat-Shock Proteins / chemistry*
  • HSP70 Heat-Shock Proteins / genetics
  • HSP70 Heat-Shock Proteins / metabolism*
  • Humans
  • Mitochondria / metabolism
  • Models, Molecular
  • Molecular Chaperones
  • Protein Binding
  • Protein Transport*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Unfolded Protein Response*

Substances

  • Carrier Proteins
  • HSP70 Heat-Shock Proteins
  • Molecular Chaperones