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第6章 分泌途径中的蛋白质分选

Chapter 6 Protein Sorting in the Secretory Pathway.

作者信息

Rodriguez-Boulan Enrique, Misek David E, Salas Dora Vega De, Salas Pedro J I, Bard Enzo

机构信息

Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York.

Department of Pathology, State University of New York, Downstate Medical Center, Brooklyn, New York.

出版信息

Curr Top Membr Transp. 1985;24:251-294. doi: 10.1016/S0070-2161(08)60328-7. Epub 2008 May 30.

Abstract

This chapter focuses on protein sorting in the secretory pathway. From primary and secondary biosynthetic sites in the cytosol and mitochondrial matrix, respectively, proteins and lipids are distributed to more than 30 final destinations in membranes or membrane-bound spaces, where they carry out their programmed function. Molecular sorting is defined, in its most general sense, as the sum of the mechanisms that determine the distribution of a given molecule from its site of synthesis to its site of function in the cell. The final site of residence of a protein in a eukaryotic cell is determined by a combination of various factors, acting in concert: (1) site of synthesis, (2) sorting signals or zip codes, (3) signal recognition or decoding mechanisms, (4) cotranslational or posttranslational mechanisms for translocation across membranes, (5) specific fusion-fission interactions between intracellular vesicular compartments, and (6) restrictions to the lateral mobility in the plane of the bilayer. Improvements in cell fractionation, protein separation, and immune precipitation procedures in the past decade have made them possible. Very little is known about the mechanisms that mediate the localization and concentration of specific proteins and lipids within organelles. Various experimental model systems have become available for their study. The advent of recombinant DNA technology has shortened the time needed for obtaining the primary structure of proteins to a few months.

摘要

本章重点关注分泌途径中的蛋白质分选。蛋白质和脂质分别从胞质溶胶和线粒体基质中的一级和二级生物合成位点,被分配到膜或膜结合空间中的30多个最终目的地,在那里它们执行其预定功能。分子分选在最一般的意义上被定义为决定给定分子从其合成位点到其在细胞内功能位点分布的机制总和。真核细胞中蛋白质的最终驻留位点由多种协同作用的因素共同决定:(1)合成位点,(2)分选信号或邮政编码,(3)信号识别或解码机制,(4)跨膜转运的共翻译或翻译后机制,(5)细胞内囊泡区室之间的特定融合-裂变相互作用,以及(6)对双层平面内横向流动性的限制。过去十年中细胞分级分离、蛋白质分离和免疫沉淀程序的改进使这些成为可能。关于介导特定蛋白质和脂质在细胞器内定位和浓缩的机制,人们了解甚少。各种实验模型系统已可用于对它们的研究。重组DNA技术的出现将获得蛋白质一级结构所需的时间缩短至几个月。

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