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大肠杆菌F1F0 ATP合酶亚基a、b和c膜插入的信号肽/信号识别颗粒需求及能量学

Sec/SRP requirements and energetics of membrane insertion of subunits a, b, and c of the Escherichia coli F1F0 ATP synthase.

作者信息

Yi Liang, Celebi Nil, Chen Minyong, Dalbey Ross E

机构信息

Department of Chemistry, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Biol Chem. 2004 Sep 17;279(38):39260-7. doi: 10.1074/jbc.M405490200. Epub 2004 Jul 19.

Abstract

Previously, the role of YidC in the membrane protein biogenesis of the F(0) sector of the Escherichia coli F(1)F(0) ATP synthase was investigated. Whereas subunits a and c of the F(1)F(0) ATP synthase were strictly dependent on YidC for membrane insertion, subunit b required YidC for efficient insertion (Yi, L., Jiang, F., Chen, M., Cain, B., Bolhuis, A., and Dalbey, R. E. (2003) Biochemistry 42, 10537-10544). In this paper, we investigated other protein components and energetics that are required in the membrane protein assembly of the F(0) sector subunits. We show here that the Sec translocase and the signal recognition particle (SRP) pathway are required for membrane insertion of subunits a and b. In contrast, subunit c required neither the Sec machinery nor the SRP pathway for insertion. While the proton motive force was not required for insertion of subunits b and c, it was required for translocation of the negatively charged periplasmic NH(2)-terminal tail of subunit a, whereas periplasmic loop 2 of subunit a could insert in a proton motive force-independent manner. Taken together, the in vivo data suggest that subunits a and b are inserted by the Sec/SRP pathway with the help of YidC, and subunit c is integrated into the membrane by the novel YidC pathway.

摘要

此前,对YidC在大肠杆菌F₁F₀ ATP合酶F₀区段膜蛋白生物合成中的作用进行了研究。F₁F₀ ATP合酶的亚基a和c的膜插入严格依赖YidC,而亚基b的有效插入需要YidC(Yi, L., Jiang, F., Chen, M., Cain, B., Bolhuis, A., and Dalbey, R. E. (2003) Biochemistry 42, 10537 - 10544)。在本文中,我们研究了F₀区段亚基膜蛋白组装中所需的其他蛋白质成分和能量学。我们在此表明,Sec转位酶和信号识别颗粒(SRP)途径是亚基a和b膜插入所必需的。相比之下,亚基c的插入既不需要Sec机制也不需要SRP途径。虽然亚基b和c的插入不需要质子动力势,但亚基a带负电荷的周质NH₂末端尾巴的转运需要质子动力势,而亚基a的周质环2可以以不依赖质子动力势的方式插入。综上所述,体内数据表明亚基a和b在YidC的帮助下通过Sec/SRP途径插入,而亚基c通过新的YidC途径整合到膜中。

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