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吲哚基-吡啶基-丙烯酮通过抑制PIKFYVE诱导自噬性程序性坏死。

Indolyl-Pyridinyl-Propenone-Induced Methuosis through the Inhibition of PIKFYVE.

作者信息

Cho Hyelim, Geno Erin, Patoor Maude, Reid Adam, McDonald Rick, Hild Marc, Jenkins Jeremy L

机构信息

Chemical Biology and Therapeutics, Novartis Institutes for BioMedical Research, 181 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.

Department of Chemistry, Johns Hopkins University, 3400 N. Charles Street, Baltimore, Maryland 21218, United States.

出版信息

ACS Omega. 2018 Jun 30;3(6):6097-6103. doi: 10.1021/acsomega.8b00202. Epub 2018 Jun 5.

Abstract

Methuosis is a form of nonapoptotic cell death characterized by the accumulation of macropinosome-derived vacuoles. Herein, we identify PIKFYVE, a class III phosphoinositide (PI) kinase, as the protein target responsible for the methuosis-inducing activity of indolyl-pyridinyl-propenones (3-(5-methoxy-2-methyl-1-indol-3-yl)-1-(4-pyridinyl)-2-propen-1-one). We further characterize the effects of chemical substitutions at the 2- and 5-indolyl positions on cytoplasmic vacuolization and PIKFYVE binding and inhibitory activity. Our study provides a better understanding of the mechanism of methuosis-inducing indolyl-pyridinyl-propenones.

摘要

巨泡性变是一种非凋亡性细胞死亡形式,其特征是巨吞饮体来源的液泡积累。在此,我们鉴定出III类磷酸肌醇(PI)激酶PIKFYVE是负责吲哚基吡啶基丙烯酮(3-(5-甲氧基-2-甲基-1-吲哚-3-基)-1-(4-吡啶基)-2-丙烯-1-酮)诱导巨泡性变活性的蛋白质靶点。我们进一步表征了2-和5-吲哚基位置的化学取代对细胞质空泡化以及PIKFYVE结合和抑制活性的影响。我们的研究有助于更好地理解吲哚基吡啶基丙烯酮诱导巨泡性变的机制。

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