A Janus-Faced IM30 Ring Involved in Thylakoid Membrane Fusion Is Assembled from IM30 Tetramers

Structure. 2017 Sep 5;25(9):1380-1390.e5. doi: 10.1016/j.str.2017.07.001. Epub 2017 Aug 10.

Abstract

Biogenesis and dynamics of thylakoid membranes likely involves membrane fusion events. Membrane attachment of the inner membrane-associated protein of 30 kDa (IM30) affects the structure of the lipid bilayer, finally resulting in membrane fusion. Yet, how IM30 triggers membrane fusion is largely unclear. IM30 monomers pre-assemble into stable tetrameric building blocks, which further align to form oligomeric ring structures, and differently sized IM30 rings bind to membranes. Based on a 3D reconstruction of IM30 rings, we locate the IM30 loop 2 region at the bottom of the ring and show intact membrane binding but missing fusogenic activity of loop 2 mutants. However, helix 7, which has recently been shown to mediate membrane binding, was located at the oppossite, top side of IM30 rings. We propose that a two-sided IM30 ring complex connects two opposing membranes, finally resulting in membrane fusion. Thus, IM30-mediated membrane fusion requires a Janus-faced IM30 ring.

Keywords: PspA; Vipp1; membrane biogenesis; membrane fusion; structure; thylakoid membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chloroplast Proteins / chemistry*
  • Chloroplast Proteins / metabolism*
  • Liposomes / metabolism
  • Membrane Fusion
  • Models, Molecular
  • Protein Binding
  • Protein Multimerization
  • Thylakoids / ultrastructure*

Substances

  • Chloroplast Proteins
  • Liposomes