open access publication

Article, 2020

An inventory of interactors of the human HSP60/HSP10 chaperonin in the mitochondrial matrix space

CELL STRESS & CHAPERONES, ISSN 1355-8145, 1355-8145, Volume 25, 3, Pages 407-416, 10.1007/s12192-020-01080-6

Contributors

Bie, Anne [1] Comert, Cagla 0000-0001-9905-3644 [1] Koerner, Roman [2] Corydon, Thomas J. 0000-0003-3588-6350 [1] Palmfeldt, Johan 0000-0001-5585-639X [1] Hipp, Mark 0000-0002-0497-3016 [2] [3] [4] Hartl, F. Ulrich 0000-0002-7941-135X [2] Bross, Peter 0000-0001-9526-8525 (Corresponding author) [1]

Affiliations

  1. [1] Aarhus Univ Hosp, Dept Ophthalmol, Palle Juul Jensens Blvd 99, DK-8200 Aarhus N, Denmark
  2. [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Max Planck Inst Biochem, Dept Cellular Biochem, Klopferspitz 18, D-82152 Martinsried, Germany
  4. [NORA names: Germany; Europe, EU; OECD];
  5. [3] Carl von Ossietzky Univ Oldenburg, Sch Med & Hlth Sci, D-26111 Oldenburg, Germany
  6. [NORA names: Germany; Europe, EU; OECD];
  7. [4] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Sci Cells & Syst, Antonius Deusinglaan 1, NL-9713 AV Groningen, Netherlands
  8. [NORA names: Netherlands; Europe, EU; OECD]

Abstract

The HSP60/HSP10 chaperonin assists folding of proteins in the mitochondrial matrix space by enclosing them in its central cavity. The chaperonin forms part of the mitochondrial protein quality control system. It is essential for cellular survival and mutations in its subunits are associated with rare neurological disorders. Here we present the first survey of interactors of the human mitochondrial HSP60/HSP10 chaperonin. Using a protocol involving metabolic labeling of HEK293 cells, cross-linking, and immunoprecipitation of HSP60, we identified 323 interacting proteins. As expected, the vast majority of these proteins are localized to the mitochondrial matrix space. We find that approximately half of the proteins annotated as mitochondrial matrix proteins interact with the HSP60/HSP10 chaperonin. They cover a broad spectrum of functions and metabolic pathways including the mitochondrial protein synthesis apparatus, the respiratory chain, and mitochondrial protein quality control. Many of the genes encoding HSP60 interactors are annotated as disease genes. There is a correlation between relative cellular abundance and relative abundance in the HSP60 immunoprecipitates. Nineteen abundant matrix proteins occupy more than 60% of the HSP60/HSP10 chaperonin capacity. The reported inventory of interactors can form the basis for interrogating which proteins are especially dependent on the chaperonin.

Keywords

Chaperonin, HSP10, HSP60, Mitochondrial protein quality control, Molecular chaperone, Protein folding

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