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蛋白质跨内质网膜的转运

Translocation of proteins across the endoplasmic reticulum membrane.

作者信息

Brodsky J L

机构信息

Department of Biological Sciences, University of Pittsburgh, Pennsylvania 15260, USA.

出版信息

Int Rev Cytol. 1998;178:277-328. doi: 10.1016/s0074-7696(08)62139-7.

Abstract

Secretory protein biogenesis begins with the insertion of a preprotein into the lumen of the endoplasmic reticulum (ER). This insertion event, known as ER protein translocation, can occur either posttranslationally, in which the preprotein is completely synthesized on cytosolic ribosomes before being translocated, or cotranslationally, in which membrane-associated ribosomes direct the nascent polypeptide chain into the ER concomitant with polypeptide elongation. In either case, preproteins are targeted to the ER membrane through specific interactions with cytosolic and/or ER membrane factors. The preprotein is then transferred to a multiprotein translocation machine in the ER membrane that includes a pore through which the preprotein passes into the ER lumen. The energy required to drive protein translocation may derive either from the coupling of translation to translocation (during cotranslational translocation) or from ER lumenal molecular chaperones that may harness the preprotein or regulate the translocation machinery (during posttranslational translocation).

摘要

分泌蛋白的生物合成始于前体蛋白插入内质网(ER)腔。这种插入事件,即ER蛋白易位,可通过翻译后方式发生,即前体蛋白在胞质核糖体上完全合成后再进行易位;也可通过共翻译方式发生,即膜结合核糖体在多肽链延伸的同时将新生多肽链直接导向内质网。无论哪种情况,前体蛋白都是通过与胞质和/或内质网膜因子的特定相互作用被靶向运输到内质网膜。然后,前体蛋白被转移到内质网膜上的一个多蛋白易位机器中,该机器包括一个孔道,前体蛋白通过此孔道进入内质网腔。驱动蛋白易位所需的能量要么来自翻译与易位的偶联(共翻译易位期间),要么来自内质网腔分子伴侣,这些分子伴侣可能利用前体蛋白或调节易位机器(翻译后易位期间)。

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