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内质网相关降解:规则之外的例外情况。

Endoplasmic reticulum-associated degradation: exceptions to the rule.

作者信息

Schmitz Anton, Herzog Volker

机构信息

Institut für Zellbiologie, Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany.

出版信息

Eur J Cell Biol. 2004 Oct;83(10):501-9. doi: 10.1078/0171-9335-00412.

Abstract

Quality control mechanisms in the endoplasmic reticulum (ER) ensure that misfolded proteins are recognized and targeted for degradation. According to the current view of ER-associated degradation (ERAD), the degradation does not occur in the ER itself but requires the retrotranslocation of the proteins to the cytosol where they are degraded by proteasomes. Although this model appears to be valid for many different proteins a number of exceptions from this rule suggest that additional proteasome-independent ERAD pathways may exist. In this review, we will summarize what is known about these alternative ERAD pathways.

摘要

内质网(ER)中的质量控制机制可确保识别错误折叠的蛋白质并将其靶向降解。根据目前内质网相关降解(ERAD)的观点,降解并非发生在内质网本身,而是需要蛋白质逆向转运至胞质溶胶,在那里它们被蛋白酶体降解。尽管该模型似乎对许多不同的蛋白质都有效,但有一些例外情况表明可能存在其他不依赖蛋白酶体的ERAD途径。在本综述中,我们将总结关于这些替代ERAD途径的已知信息。

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