Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605-2324, USA.
Trends Biochem Sci. 2012 Aug;37(8):303-8. doi: 10.1016/j.tibs.2012.05.003. Epub 2012 Jun 29.
Integration of a protein into the endoplasmic reticulum (ER) membrane occurs through a series of multistep reactions that include targeting of ribosome-nascent polypeptide complexes to the ER, attachment of the ribosome to the protein translocation channel, lateral partitioning of α-helical transmembrane spans into the lipid bilayer, and folding of the lumenal, cytosolic and membrane-embedded domains of the protein. However, the molecular mechanisms and kinetics of these steps are still not entirely clear. To obtain a better understanding of the mechanism of membrane protein integration, we propose that it will be important to utilize in vivo experiments to examine the kinetics of membrane protein integration and in vitro experiments to characterize interactions between nascent membrane proteins, protein translocation factors and molecular chaperones.
蛋白质整合到内质网(ER)膜中是通过一系列多步骤反应进行的,包括核糖体-新生多肽复合物靶向 ER、核糖体附着到蛋白质易位子通道、α-螺旋跨膜结构域横向分配到脂质双层以及蛋白质的腔、细胞质和膜嵌入结构域的折叠。然而,这些步骤的分子机制和动力学仍然不完全清楚。为了更好地理解膜蛋白整合的机制,我们认为利用体内实验来研究膜蛋白整合的动力学以及体外实验来表征新生膜蛋白、蛋白易位子因子和分子伴侣之间的相互作用将是很重要的。