Structural basis of respiratory complex adaptation to cold temperatures

Cell. 2024 Nov 14;187(23):6584-6598.e17. doi: 10.1016/j.cell.2024.09.029. Epub 2024 Oct 11.

Abstract

In response to cold, mammals activate brown fat for respiratory-dependent thermogenesis reliant on the electron transport chain. Yet, the structural basis of respiratory complex adaptation upon cold exposure remains elusive. Herein, we combined thermoregulatory physiology and cryoelectron microscopy (cryo-EM) to study endogenous respiratory supercomplexes from mice exposed to different temperatures. A cold-induced conformation of CI:III2 (termed type 2) supercomplex was identified with a ∼25° rotation of CIII2 around its inter-dimer axis, shortening inter-complex Q exchange space, and exhibiting catalytic states that favor electron transfer. Large-scale supercomplex simulations in mitochondrial membranes reveal how lipid-protein arrangements stabilize type 2 complexes to enhance catalytic activity. Together, our cryo-EM studies, multiscale simulations, and biochemical analyses unveil the thermoregulatory mechanisms and dynamics of increased respiratory capacity in brown fat at the structural and energetic level.

Keywords: CIII(2) rotation; brown adipose tissue; cellular adaptation; electron transport chain; membrane lipid remodeling; respiratory complexes.

MeSH terms

  • Adaptation, Physiological
  • Adipose Tissue, Brown* / metabolism
  • Animals
  • Body Temperature Regulation / physiology
  • Cold Temperature*
  • Cryoelectron Microscopy*
  • Electron Transport
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Mitochondria / ultrastructure
  • Mitochondrial Membranes / metabolism
  • Thermogenesis* / physiology