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线粒体通过细胞器和蛋白质降解进行质量控制。

Mitochondrial quality control via organelle and protein degradation.

机构信息

Department of Biomolecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.

Department of Biosciences, School of Science, Kitasato University, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0373, Japan.

出版信息

J Biochem. 2024 Apr 29;175(5):487-494. doi: 10.1093/jb/mvad106.

Abstract

Mitochondria are essential eukaryotic organelles that produce ATP as well as synthesize various macromolecules. They also participate in signalling pathways such as the innate immune response and apoptosis. These diverse functions are performed by >1,000 different mitochondrial proteins. Although mitochondria are continuously exposed to potentially damaging conditions such as reactive oxygen species, proteases/peptidases localized in different mitochondrial subcompartments, termed mitoproteases, maintain mitochondrial quality and integrity. In addition to processing incoming precursors and degrading damaged proteins, mitoproteases also regulate metabolic reactions, mitochondrial protein half-lives and gene transcription. Impaired mitoprotease function is associated with various pathologies. In this review, we highlight recent advances in our understanding of mitochondrial quality control regulated by autophagy, ubiquitin-proteasomes and mitoproteases.

摘要

线粒体是真核生物中必不可少的细胞器,它们不仅可以产生 ATP,还可以合成各种大分子。线粒体还参与了许多信号通路,如先天免疫反应和细胞凋亡。这些不同的功能是由超过 1000 种不同的线粒体蛋白来完成的。尽管线粒体不断受到潜在有害条件的影响,如活性氧物种、定位在不同线粒体亚区室中的蛋白酶/肽酶(称为线粒体蛋白酶),但它们可以维持线粒体的质量和完整性。除了加工输入的前体和降解受损的蛋白质外,线粒体蛋白酶还调节代谢反应、线粒体蛋白半衰期和基因转录。线粒体蛋白酶功能受损与各种病理有关。在这篇综述中,我们强调了最近在自噬、泛素-蛋白酶体和线粒体蛋白酶调控的线粒体质量控制方面的理解进展。

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