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靶向线粒体复合体I的新型自噬抑制剂奥米汀的发现。

Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I.

作者信息

Robke Lucas, Futamura Yushi, Konstantinidis Georgios, Wilke Julian, Aono Harumi, Mahmoud Zhwan, Watanabe Nobumoto, Wu Yao-Wen, Osada Hiroyuki, Laraia Luca, Waldmann Herbert

机构信息

Max-Planck-Institute of Molecular Physiology , Department of Chemical Biology , Otto-Hahn-Str. 11 , 44227 Dortmund , Germany.

Faculty of Chemistry and Chemical Biology , TU Dortmund University , Otto-Hahn-Str. 4a , 44227 Dortmund , Germany . Email:

出版信息

Chem Sci. 2018 Feb 26;9(11):3014-3022. doi: 10.1039/c7sc05040b. eCollection 2018 Mar 21.

Abstract

Macroautophagy is a conserved eukaryotic process for degradation of cellular components in response to lack of nutrients. It is involved in the development of diseases, notably cancer and neurological disorders including Parkinson's disease. Small molecule autophagy modulators have proven to be valuable tools to dissect and interrogate this crucial metabolic pathway and are in high demand. Phenotypic screening for autophagy inhibitors led to the discovery of the novel autophagy inhibitor aumitin. Target identification and confirmation revealed that aumitin inhibits mitochondrial respiration by targeting complex I. We show that inhibition of autophagy by impairment of mitochondrial respiration is general for several mitochondrial inhibitors that target different mitochondrial complexes. Our findings highlight the importance of mitochondrial respiration for autophagy regulation.

摘要

巨自噬是一种保守的真核细胞过程,用于在营养物质缺乏时降解细胞成分。它参与疾病的发展,特别是癌症和包括帕金森病在内的神经疾病。小分子自噬调节剂已被证明是剖析和研究这一关键代谢途径的有价值工具,且需求旺盛。对自噬抑制剂的表型筛选导致了新型自噬抑制剂奥米汀的发现。靶点鉴定和确认表明,奥米汀通过靶向复合体I抑制线粒体呼吸。我们发现,通过损害线粒体呼吸来抑制自噬对于几种靶向不同线粒体复合体的线粒体抑制剂来说是普遍现象。我们的研究结果突出了线粒体呼吸对自噬调节的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7232/5916016/81b6a0c9bc98/c7sc05040b-f1.jpg

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