Eeyarestatin Compounds Selectively Enhance Sec61-Mediated Ca 2+ Leakage from the Endoplasmic Reticulum.
Cell Chemical Biology(2019)
摘要
Eeyarestatin 1 (ES1) inhibits p97-dependent protein degradation, Sec61-dependent protein translocation into the endoplasmic reticulum (ER), and vesicular transport within the endomembrane system. Here, we show that ES1 impairs Ca2+ homeostasis by enhancing the Ca2+ leakage from mammalian ER. A comparison of various ES1 analogs suggested that the 5-nitrofuran (5-NF) ring of ES1 is crucial for this effect. Accordingly, the analog ES24, which conserves the 5-NF domain of ES1, selectively inhibited protein translocation into the ER, displayed the highest potency on ER Ca2+ leakage of ES1 analogs studied and induced Ca2+-dependent cell death. Using small interfering RNA-mediated knockdown of Sec61α, we identified Sec61 complexes as the targets that mediate the gain of Ca2+ leakage induced by ES1 and ES24. By interacting with the lateral gate of Sec61α, ES1 and ES24 likely capture Sec61 complexes in a Ca2+-permeable, open state, in which Sec61 complexes allow Ca2+ leakage but are translocation incompetent.
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关键词
calcium homeostasis,eeyarestatin,endoplasmic reticulum,endoplasmic reticulum calcium content,endoplasmic reticulum calcium homeostasis,endoplasmic reticulum calcium leakage,translocon of endoplasmic reticulum,Sec61 complexes of the endoplasmic reticulum,Protein translocation and degradation,calcium-dependent cytotoxicity
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