Tricalbin-Mediated Contact Sites Control ER Curvature to Maintain Plasma Membrane Integrity

Dev Cell. 2019 Nov 18;51(4):476-487.e7. doi: 10.1016/j.devcel.2019.10.018.

Abstract

Membrane contact sites (MCS) between the endoplasmic reticulum (ER) and the plasma membrane (PM) play fundamental roles in all eukaryotic cells. ER-PM MCS are particularly abundant in Saccharomyces cerevisiae, where approximately half of the PM surface is covered by cortical ER (cER). Several proteins, including Ist2, Scs2/22, and Tcb1/2/3 are implicated in cER formation, but the specific roles of these molecules are poorly understood. Here, we use cryo-electron tomography to show that ER-PM tethers are key determinants of cER morphology. Notably, Tcb proteins (tricalbins) form peaks of extreme curvature on the cER membrane facing the PM. Combined modeling and functional assays suggest that Tcb-mediated cER peaks facilitate the transport of lipids between the cER and the PM, which is necessary to maintain PM integrity under heat stress. ER peaks were also present at other MCS, implying that membrane curvature enforcement may be a widespread mechanism to regulate MCS function.

Keywords: cryo-ET; cryo-FIB; cryo-electron tomography; cryo-focused ion beam milling; endoplasmic reticulum; membrane contact site; membrane curvature; plasma membrane; tricalbins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium-Binding Proteins / metabolism*
  • Cell Membrane / metabolism*
  • Cell Membrane / physiology
  • Cryoelectron Microscopy / methods
  • Endoplasmic Reticulum / metabolism*
  • Lipids
  • Membrane Proteins / metabolism
  • Mitochondria / physiology
  • Mitochondrial Membranes / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • Calcium-Binding Proteins
  • IST2 protein, S cerevisiae
  • Lipids
  • Membrane Proteins
  • Saccharomyces cerevisiae Proteins
  • Scs2 protein, S cerevisiae
  • TCB1 protein, S cerevisiae