Terlecky S R, Wiemer E A, Nuttley W M, Walton P A, Subramani S
Department of Biology, University of California, San Diego, La Jolla 92093-0322, USA.
Ann N Y Acad Sci. 1996 Dec 27;804:11-20. doi: 10.1111/j.1749-6632.1996.tb18604.x.
Peroxisomes are ubiquitous eukaryotic organelles which function in a wide variety of metabolic processes. The many lethal human disorders associated with defects in peroxisomal protein import underscore the importance of this organelle. In recent years, the evolutionarily conserved molecular mechanisms of protein targeting to, and translocation across, peroxisomal membranes have begun to emerge. Signals which route proteins to the organelle have been identified, as have cytosolic, membrane-associated, and lumenal components of the import machinery. The goal of this brief review was to summarize our current knowledge of some of these molecules and to describe several potential mechanisms by which peroxisomes selectively import their constituent proteins. Aspects of these mechanisms that distinguish peroxisomal protein import from protein targeting to other organelles are highlighted.
过氧化物酶体是普遍存在的真核细胞器,在多种代谢过程中发挥作用。许多与过氧化物酶体蛋白输入缺陷相关的致命人类疾病突出了这种细胞器的重要性。近年来,蛋白质靶向过氧化物酶体膜并穿过过氧化物酶体膜的进化保守分子机制已开始显现。已鉴定出将蛋白质导向该细胞器的信号,以及输入机制的胞质、膜相关和腔成分。这篇简短综述的目的是总结我们目前对其中一些分子的了解,并描述过氧化物酶体选择性输入其组成蛋白的几种潜在机制。重点介绍了这些机制中使过氧化物酶体蛋白输入区别于蛋白质靶向其他细胞器的方面。