bioRxiv · 10.1101/2024.01.16.575914
Structural basis of respiratory complexes adaptation to cold temperatures
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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Shin, Y.-C., Latorre-Muro, P., Djurabekova, A., Zdorevskyi, O., Bennett, C., Burger, N., Song, K., Xu, C., Sharma, V., Liao, M., Puigserver, P.. 2024-01-17. Structural basis of respiratory complexes adaptation to cold temperatures. https://doi.org/10.1101/2024.01.16.575914
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