Max-Planck-Institut für Biochemie, Am Klopferspitz 18, 82152 Martinsried, Germany.
J Struct Biol. 2012 Aug;179(2):121-5. doi: 10.1016/j.jsb.2012.04.019. Epub 2012 May 7.
The family of AAA+ proteins in eukaryotes has many members in various cellular compartments with a broad spectrum of functions in protein unfolding and degradation. The mitochondrial AAA protein Bcs1 plays an unusual role in protein translocation. It is involved in the topogenesis of the Rieske protein, Rip1, and thereby in the biogenesis of the cytochrome bc(1) complex of the mitochondrial respiratory chain. Bcs1 mediates the export of the folded FeS domain of Rip1 across the mitochondrial inner membrane and the insertion of its transmembrane segment into an assembly intermediate of the cytochrome bc(1) complex. We discuss structural elements of the Bcs1 protein compared to other AAA proteins in an attempt to understand the mechanism of its function. In this context, we discuss human diseases caused by mutations in Bcs1 that lead to different properties of the protein and subsequently to different symptoms.
真核生物 AAA+ 蛋白家族在各种细胞区室中有许多成员,其功能广泛涉及蛋白展开和降解。线粒体 AAA 蛋白 Bcs1 在蛋白易位中扮演着特殊的角色。它参与 Rieske 蛋白 Rip1 的拓扑发生,从而参与线粒体呼吸链细胞色素 bc(1) 复合物的生物发生。Bcs1 介导 Rip1 的折叠 FeS 结构域穿过线粒体内膜的输出,以及其跨膜片段插入细胞色素 bc(1) 复合物组装中间体。我们比较了 Bcs1 蛋白与其他 AAA 蛋白的结构元件,试图理解其功能的机制。在这方面,我们讨论了由 Bcs1 突变引起的人类疾病,这些突变导致蛋白质的不同性质,进而导致不同的症状。