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

机译:靶向线粒体复合体I的新型自噬抑制剂铝蛋白的发现

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摘要

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.
机译:巨自噬是一种保守的真核生物过程,用于响应缺乏营养而降解细胞成分。它参与疾病的发展,特别是癌症和神经系统疾病,包括帕金森氏病。小分子自噬调节剂已被证明是解析和询问这一关键代谢途径的有价值的工具,并且需求量很大。自噬抑制剂的表型筛选导致新型自噬抑制剂铝蛋白的发现。目标识别和确认表明,铝蛋白通过靶向复合物I抑制线粒体呼吸。我们表明,针对几种针对不同线粒体复合物的线粒体抑制剂,通过线粒体呼吸损害的抑制来抑制自噬是普遍的。我们的发现突出了线粒体呼吸对于自噬调节的重要性。

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