The structure and function of P5A-ATPases

Nat Commun. 2024 Nov 6;15(1):9605. doi: 10.1038/s41467-024-53757-6.

Abstract

Endoplasmic reticulum (ER) membrane resident P5A-ATPases broadly affect protein biogenesis and quality control, and yet their molecular function remains debated. Here, we report cryo-EM structures of a P5A-ATPase, CtSpf1, covering multiple transport intermediates of the E1 → E1-ATP → E1P-ADP → E1P → E2P → E2.Pi → E2 → E1 cycle. In the E2P and E2.Pi states a cleft spans the entire membrane, holding a polypeptide cargo molecule. The cargo includes an ER luminal extension, pinpointed as the C-terminus in the E2.Pi state, which reenters the membrane in E2P. The E1 structure harbors a cytosol-facing cavity that is blocked by an insertion we refer to as the Plug-domain. The Plug-domain is nestled to key ATPase features and is displaced in the E1P-ADP and E1P states. Collectively, our findings are compatible with a broad range of proteins as cargo, with the P5A-ATPases serving a role in membrane removal of helices, although insertion/secretion cannot be excluded, as well as with a mechanistic role of the Plug-domain.

MeSH terms

  • Adenosine Triphosphatases* / chemistry
  • Adenosine Triphosphatases* / genetics
  • Adenosine Triphosphatases* / metabolism
  • Adenosine Triphosphate / metabolism
  • Chaetomium / enzymology
  • Chaetomium / genetics
  • Chaetomium / metabolism
  • Cryoelectron Microscopy*
  • Endoplasmic Reticulum* / metabolism
  • Models, Molecular
  • Protein Domains

Substances

  • Adenosine Triphosphatases
  • Adenosine Triphosphate

Supplementary concepts

  • Chaetomium thermophilum