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Tim9p在TIM22导入复合体组装中的作用。

The role of Tim9p in the assembly of the TIM22 import complexes.

作者信息

Leuenberger Danielle, Curran Sean P, Wong David, Koehler Carla M

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095-1569, USA.

出版信息

Traffic. 2003 Mar;4(3):144-52. doi: 10.1034/j.1600-0854.2003.00095.x.

Abstract

Tim9p is located in the soluble 70-kDa Tim9p-Tim10p complex and the 300-kDa membrane complex in the mitochondrial TIM22 protein import system, which mediates the import of inner membrane proteins. From a collection of temperature-sensitive mutants, we have analyzed two in detail. tim9-3 contained two mutations and tim9-19 contained one mutation, all located near the 'twin CX3C' motif that is conserved in the small Tim proteins. As a result, the import components in the tim9-3 mutant mitochondria were severely reduced and assembled into complexes of aberrant sizes. Protein import was severely reduced and Tim9p and Tim10p binding to in vitro imported ADP/ATP carrier was impaired. In the tim9-19 mutant mitochondria, the 300-kDa membrane complex was assembled, although the soluble 70-kDa Tim9p-Tim10p complex was not detectable. Protein import was decreased only two-fold. When coexpressed in Escherichia coli, tim9-19 and TIM10 proteins failed to assemble into a 70-kDa complex. Our findings suggest that residues near the 'twin CX3C' motif are important for the assembly of Tim9p in both the Tim9p-Tim10p complex and the 300-kDa membrane complex.

摘要

Tim9p存在于线粒体TIM22蛋白导入系统中的可溶性70 kDa Tim9p - Tim10p复合体以及300 kDa膜复合体中,该系统介导内膜蛋白的导入。从一组温度敏感突变体中,我们详细分析了两个突变体。tim9 - 3含有两个突变,tim9 - 19含有一个突变,所有突变均位于小Tim蛋白中保守的“双CX3C”基序附近。结果,tim9 - 3突变体线粒体中的导入成分严重减少,并组装成异常大小的复合体。蛋白导入严重减少,Tim9p和Tim10p与体外导入的ADP / ATP载体的结合受损。在tim9 - 19突变体线粒体中,300 kDa膜复合体组装完成,尽管未检测到可溶性70 kDa Tim9p - Tim10p复合体。蛋白导入仅降低了两倍。当在大肠杆菌中共表达时,tim9 - 19和TIM10蛋白无法组装成70 kDa复合体。我们的研究结果表明,“双CX3C”基序附近的残基对于Tim9p在Tim9p - Tim10p复合体和300 kDa膜复合体中的组装都很重要。

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