Department of Molecular and Cellular Biology, Harvard University, Northwest Laboratories, Cambridge, Massachusetts 02138, USA.
Cold Spring Harb Perspect Biol. 2013 Aug 1;5(8):a013334. doi: 10.1101/cshperspect.a013334.
Hundreds of eukaryotic membrane proteins are anchored to membranes by a single transmembrane domain at their carboxyl terminus. Many of these tail-anchored (TA) proteins are posttranslationally targeted to the endoplasmic reticulum (ER) membrane for insertion by the guided-entry of TA protein insertion (GET) pathway. In recent years, most of the components of this conserved pathway have been biochemically and structurally characterized. Get3 is the pathway-targeting factor that uses nucleotide-linked conformational changes to mediate the delivery of TA proteins between the GET pretargeting machinery in the cytosol and the transmembrane pathway components in the ER. Here we focus on the mechanism of the yeast GET pathway and make a speculative analogy between its membrane insertion step and the ATPase-driven cycle of ABC transporters.
数百种真核膜蛋白通过其羧基末端的单个跨膜结构域锚定在膜上。这些尾部锚定(TA)蛋白中的许多是通过靶向 TA 蛋白插入(GET)途径的内质网(ER)膜进行翻译后靶向定位的。近年来,该保守途径的大多数成分已在生化和结构上进行了表征。Get3 是途径靶向因子,它利用核苷酸连接的构象变化来介导 TA 蛋白在细胞质中的 GET 前靶向机制与 ER 中的跨膜途径成分之间的递呈。在这里,我们专注于酵母 GET 途径的机制,并对其膜插入步骤与 ABC 转运体的 ATP 酶驱动循环进行推测性类比。