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内质网与衰老——蛋白质折叠及内质网应激反应

ER and aging-Protein folding and the ER stress response.

作者信息

Naidoo Nirinjini

机构信息

Center for Sleep and Respiratory Neurobiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, United States.

出版信息

Ageing Res Rev. 2009 Jul;8(3):150-9. doi: 10.1016/j.arr.2009.03.001. Epub 2009 Mar 21.

Abstract

The endoplasmic reticulum (ER) is a multifunctional organelle which co-ordinates protein folding, lipid biosynthesis, calcium storage and release. Perturbations that disrupt ER homeostasis lead to the misfolding of proteins, ER stress and up-regulation of a signaling pathway called the ER stress response or the unfolded protein response (UPR). The UPR is characterized by the induction of chaperones, degradation of misfolded proteins and attenuation of protein translation. Age-related declines and activity in key molecular chaperones and folding enzymes compromise proper protein folding and the adaptive response of the UPR. This review will highlight age-related changes in the protein folding machinery and in the UPR.

摘要

内质网(ER)是一种多功能细胞器,它协调蛋白质折叠、脂质生物合成、钙储存和释放。破坏内质网稳态的扰动会导致蛋白质错误折叠、内质网应激以及一种称为内质网应激反应或未折叠蛋白反应(UPR)的信号通路上调。UPR的特征是伴侣蛋白的诱导、错误折叠蛋白的降解以及蛋白质翻译的减弱。与年龄相关的关键分子伴侣和折叠酶的活性下降会损害蛋白质的正确折叠和UPR的适应性反应。本综述将重点介绍蛋白质折叠机制和UPR中与年龄相关的变化。

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