Structural basis of respiratory complexes adaptation to cold temperatures
Young-Cheul ShiniD, Pedro Latorre‐MuroiD, Amina DjurabekovaiD, Oleksii ZdorevskyiiD, Christopher F. BennettiD, Nils BurgeriD, Kangkang SongiD, Chen Xu, João A. PauloiD, Steven P. GygiiD, Vivek SharmaiD, Maofu LiaoiD, Pere PuigserveriD
Abstract
In response to cold, mammals activate brown fat for respiratory-dependent thermogenesis reliant on the electron transport chain (1, 2). Yet, the structural basis of respiratory complex adaptation to cold remains elusive. Herein we combined thermoregulatory physiology and cryo-EM to study endogenous respiratory supercomplexes exposed to different temperatures. A cold-induced conformation of CI:III2 (termed type 2) was identified with a [~]25{degrees} rotation of CIII2 around its inter-dimer axis, shortening inter-complex Q exchange space, and exhibiting different catalytic states which favor electron transfer. Large-scale supercomplex simulations in lipid membrane reveal how unique lipid-protein arrangements stabilize type 2 complexes to enhance catalytic activity. Together, our cryo-EM studies, multiscale simulations and biochemical analyses unveil the mechanisms and dynamics of respiratory adaptation at the structural and energetic level.
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