生物化学セミナー 総合生命科学部 生命科学セミナー 演 者 : Prof. Agnieszka Chacinska (ポーランド・ワルシャワ国際細胞生物学研究所) 日 時 : 2016年8月31日(水)16:00~17:00 場 所 : 京都産業大学総合生命科学部15号館1階 15102セミナー室 http://www.kyoto-su.ac.jp/access.html 演 題 :Oxidation of mitochondrial membrane proteins Mitochondrial proteins require essential and sophisticated machineries to reach their intramitochondrial location. The mitochondrial intermembrane space assembly (MIA) pathway is dedicated to the redox-dependent import and biogenesis of proteins localized to the intermembrane space of mitochondria. The oxidoreductase Mia40 is a central component of the pathway responsible for the transfer of disulfide bonds to intermembrane space precursor proteins causing their oxidative folding. We identified Tim22, a multispanning membrane protein and core component of the TIM22 translocase, as a protein with cysteine residues undergoing oxidation during Tim22 biogenesis. Tim22 forms a disulfide-bonded intermediate with Mia40 upon import into mitochondria. Interestingly, Mia40 binds the Tim22 precursor also via non-covalent interactions. Tim22 belongs to the Tim17/Tim22/Tim23 family of protein translocases. Disulfide bond formation in Tim17 and Tim22 are conserved among fungi and metazoan. Yeast and human Tim22 variants that are not oxidized do not properly integrate into the membrane complex. Consistently, the lack of Tim17 oxidation disrupts the TIM23 translocase complex. The findings underline the importance of disulfide bond formation for mature translocase assembly through membrane stabilization of weak transmembrane domains. Agnieszka Chacinska International Institute of Molecular and Cell Biology in Warsaw, Poland 世話人:京都産業大学総合生命科学部 遠藤 斗志也 共催 :JSPS 科研費 15H05705 「ミトコンドリア生合成を司る細胞内統合的ネットワークの解明」
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