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细胞色素c1的生物合成。细胞色素c1血红素裂解酶的作用以及导入线粒体过程中两个蛋白水解加工步骤的作用。

Biogenesis of cytochrome c1. Role of cytochrome c1 heme lyase and of the two proteolytic processing steps during import into mitochondria.

作者信息

Nicholson D W, Stuart R A, Neupert W

机构信息

Institut für Physiologische Chemie der Universität München, Federal Republic of Germany.

出版信息

J Biol Chem. 1989 Jun 15;264(17):10156-68.

PMID:2542325
Abstract

The biogenesis of cytochrome c1 involves a number of steps including: synthesis as a precursor with a bipartite signal sequence, transfer across the outer and inner mitochondrial membranes, removal of the first part of the presequence in the matrix, reexport to the outer surface of the inner membrane, covalent addition of heme, and removal of the remainder of the presequence. In this report we have focused on the steps of heme addition, catalyzed by cytochrome c1 heme lyase, and of proteolytic processing during cytochrome c1 import into mitochondria. Following translocation from the matrix side to the intermembrane-space side of the inner membrane, apocytochrome c1 forms a complex with cytochrome c1 heme lyase, and then holocytochrome c1 formation occurs. Holocytochrome c1 formation can also be observed in detergent-solubilized preparations of mitochondria, but only after apocytochrome c1 has first interacted with cytochrome c1 heme lyase to produce this complex. Heme linkage takes place on the intermembrane-space side of the inner mitochondrial membrane and is dependent on NADH plus a cytosolic cofactor that can be replaced by flavin nucleotides. NADH and FMN appear to be necessary for reduction of heme prior to its linkage to apocytochrome c1. The second proteolytic processing of cytochrome c1 does not take place unless the covalent linkage of heme to apocytochrome c1 precedes it. On the other hand, the cytochrome c1 heme lyase reaction itself does not require that processing of the cytochrome c1 precursor to intermediate size cytochrome c1 takes place first. In conclusion, cytochrome c1 heme lyase catalyzes an essential step in the import pathway of cytochrome c1, but it is not involved in the transmembrane movement of the precursor polypeptide. This is in contrast to the case for cytochrome c in which heme addition is coupled to its transport directly across the outer membrane into the intermembrane space.

摘要

细胞色素c1的生物合成涉及多个步骤,包括:作为具有双功能信号序列的前体进行合成、穿过线粒体外膜和内膜、在基质中去除前导序列的第一部分、重新输出到内膜的外表面、血红素的共价添加以及去除前导序列的其余部分。在本报告中,我们重点关注了由细胞色素c1血红素加氧酶催化的血红素添加步骤以及细胞色素c1导入线粒体过程中的蛋白水解加工步骤。从内膜的基质侧转运到膜间隙侧后,脱辅基细胞色素c1与细胞色素c1血红素加氧酶形成复合物,然后形成全细胞色素c1。在去垢剂溶解的线粒体制剂中也可以观察到全细胞色素c1的形成,但前提是脱辅基细胞色素c1首先与细胞色素c1血红素加氧酶相互作用以产生这种复合物。血红素连接发生在线粒体内膜的膜间隙侧,并且依赖于NADH加上一种可被黄素核苷酸替代的胞质辅因子。NADH和FMN似乎是血红素与脱辅基细胞色素c1连接之前还原所必需的。细胞色素c1的第二次蛋白水解加工只有在血红素与脱辅基细胞色素c1共价连接之前才会发生。另一方面,细胞色素c1血红素加氧酶反应本身并不要求首先将细胞色素c1前体加工成中等大小的细胞色素c1。总之,细胞色素c1血红素加氧酶催化细胞色素c1导入途径中的一个关键步骤,但它不参与前体多肽的跨膜移动。这与细胞色素c的情况相反,在细胞色素c中,血红素添加与它直接穿过外膜进入膜间隙的运输相偶联。

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