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蛋白酶体降解:底物进入。

Proteasome degradation: enter the substrate.

作者信息

Förster Andreas, Hill Christopher P

机构信息

Department of Biochemistry, University of Utah, Salt Lake City, UT 84132, USA.

出版信息

Trends Cell Biol. 2003 Nov;13(11):550-3. doi: 10.1016/j.tcb.2003.09.001.

Abstract

Cells depend upon the regulated destruction of their various proteins to maintain homeostasis and change their metabolic state. A key component of this process is the proteasome - a large multisubunit protease whose catalytic sites are sequestered within a central chamber. Entry of substrates into proteasomes is regulated by activators and is generally thought to proceed sequentially, starting from one end of the substrate polypeptide. This conventional view is expanded by a recent paper, which indicates that some unfolded substrates can open the entrance to the proteolytic chamber in the absence of an activator and can enter the proteasome in a hairpin conformation to allow limited proteolysis of internal segments.

摘要

细胞依靠对其各种蛋白质的有序降解来维持体内平衡并改变其代谢状态。这一过程的关键组成部分是蛋白酶体——一种大型多亚基蛋白酶,其催化位点被隔离在一个中央腔室内。底物进入蛋白酶体由激活剂调控,通常认为是从底物多肽的一端开始依次进行的。最近的一篇论文扩展了这一传统观点,该论文表明一些未折叠的底物在没有激活剂的情况下可以打开蛋白水解腔室的入口,并以发夹构象进入蛋白酶体,从而允许对内部片段进行有限的蛋白水解。

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