Abteilung für Systembiochemie, Medizinische Fakultät der Ruhr-Universität Bochum, Ruhr-Universität Bochum, Universitätsstr. 150, 44780, Bochum, Germany.
Cell Mol Life Sci. 2013 Apr;70(8):1393-411. doi: 10.1007/s00018-012-1136-9. Epub 2012 Sep 15.
Peroxisomes constitute a dynamic compartment of almost all eukaryotic cells. Depending on environmental changes and cellular demands peroxisomes can acquire diverse metabolic roles. The compartmentalization of peroxisomal matrix enzymes is a prerequisite to carry out their physiologic function. The matrix proteins are synthesized on free ribosomes in the cytosol and are ferried to the peroxisomal membrane by specific soluble receptors. Subsequent to cargo release into the peroxisomal matrix, the receptors are exported back to the cytosol to facilitate further rounds of matrix protein import. This dislocation step is accomplished by a remarkable machinery, which comprises enzymes required for the ubiquitination as well as the ATP-dependent extraction of the receptor from the membrane. Interestingly, receptor ubiquitination and dislocation are the only known energy-dependent steps in the peroxisomal matrix protein import process. The current view is that the export machinery of the receptors might function as molecular motor not only in the dislocation of the receptors but also in the import step of peroxisomal matrix protein by coupling ATP-dependent removal of the peroxisomal import receptor with cargo translocation into the organelle. In this review we will focus on the architecture and function of the peroxisomal receptor export machinery, the peroxisomal exportomer.
过氧化物酶体是几乎所有真核细胞的一个动态隔室。根据环境变化和细胞需求,过氧化物酶体可以获得不同的代谢作用。过氧化物酶体基质酶的区室化是执行其生理功能的前提。基质蛋白在细胞质中的游离核糖体上合成,并通过特定的可溶性受体被运送到过氧化物酶体膜。在货物释放到过氧化物酶体基质中之后,受体被输出回细胞质,以促进进一步的基质蛋白输入循环。这种脱位步骤是由一个显著的机制完成的,该机制包括泛素化以及受体从膜中 ATP 依赖性提取所需的酶。有趣的是,受体的泛素化和脱位是过氧化物酶体基质蛋白输入过程中唯一已知的能量依赖步骤。目前的观点是,受体的输出机制不仅可以作为分子马达在受体的脱位中发挥作用,而且可以在过氧化物酶体基质蛋白的输入步骤中发挥作用,通过将 ATP 依赖性的过氧化物酶体输入受体的去除与货物转运到细胞器耦联起来。在这篇综述中,我们将重点介绍过氧化物酶体受体输出机制(过氧化物酶体输出体)的结构和功能。