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细胞核蛋白酶体与氧化损伤蛋白的降解

The nuclear proteasome and the degradation of oxidatively damaged proteins.

作者信息

Voss P, Grune T

机构信息

Research Institute of Environmental Medicine, Heinrich Heine University, Duesseldorf, Germany.

出版信息

Amino Acids. 2007;32(4):527-34. doi: 10.1007/s00726-006-0428-5. Epub 2006 Nov 15.

Abstract

The accumulation of oxidized proteins is known to be linked to some severe neurodegenerative diseases like Alzheimer's, Parkinson's and Huntington's disease. Furthermore, the aging process is also accompanied by an ongoing aggregation of misfolded and damaged proteins. Therefore, mammalian cells have developed potent degradation systems, which selectively degrade damaged and misfolded proteins. The proteasomal system is largely responsible for the removal of oxidatively damaged proteins form the cellular environment. Not only cytosolic proteins are prone to oxidative stress, also nuclear proteins are readily oxidized. The nuclear proteasomal system is responsible for the degradation of these proteins. This review is focused on the specific degradation of oxidized nuclear proteins, the role of the proteasome in this process and the regulation of the nuclear proteasomal system under oxidative conditions.

摘要

已知氧化蛋白质的积累与一些严重的神经退行性疾病有关,如阿尔茨海默病、帕金森病和亨廷顿舞蹈症。此外,衰老过程还伴随着错误折叠和受损蛋白质的持续聚集。因此,哺乳动物细胞已发展出强大的降解系统,可选择性地降解受损和错误折叠的蛋白质。蛋白酶体系统在很大程度上负责从细胞环境中清除氧化损伤的蛋白质。不仅胞质蛋白易受氧化应激影响,核蛋白也容易被氧化。核蛋白酶体系统负责这些蛋白质的降解。本综述聚焦于氧化核蛋白的特异性降解、蛋白酶体在此过程中的作用以及氧化条件下核蛋白酶体系统的调控。

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