This is a preprint.
Structural basis of respiratory complexes adaptation to cold temperatures
- PMID: 38293190
- PMCID: PMC10827213
- DOI: 10.1101/2024.01.16.575914
Structural basis of respiratory complexes adaptation to cold temperatures
Update in
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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. Cell. 2024. PMID: 39395414
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:III 2 (termed type 2) was identified with a ∼25° rotation of CIII 2 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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