Suppr超能文献

拉贾多内和莱普霉素B通过相同机制阻断CRM1依赖性核输出。

Ratjadone and leptomycin B block CRM1-dependent nuclear export by identical mechanisms.

作者信息

Meissner Torsten, Krause Eberhard, Vinkemeier Uwe

机构信息

Abteilung Zelluläre Signalverarbeitung, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, Freie Universität Berlin, Robert-Rössle-Str. 10, 13125 Berlin, Germany.

出版信息

FEBS Lett. 2004 Oct 8;576(1-2):27-30. doi: 10.1016/j.febslet.2004.08.056.

Abstract

Research on the export of proteins and nucleic acids from the nucleus to the cytoplasm has greatly gained from the discovery that the actinobacterial toxin leptomycin B (LMB) specifically inactivates the export receptor chromosomal region maintenance 1 (CRM1). Recently, it was shown that myxobacterial cytotoxins, named ratjadones (RATs), also bind to CRM1 and inhibit nuclear export. However, the reaction mechanism of RATs was not resolved. Here, we show that LMB and RAT A employ the same molecular mechanism to inactivate CRM1. Alkylation of residue Cys528 of CRM1 determines both LMB and RAT sensitivity and prevents nuclear export of CRM1 cargo proteins.

摘要

对蛋白质和核酸从细胞核输出到细胞质的研究,因发现放线菌毒素莱普霉素B(LMB)能特异性使输出受体染色体区域维持蛋白1(CRM1)失活而受益匪浅。最近,研究表明名为鼠jadones(RATs)的黏细菌细胞毒素也能结合CRM1并抑制核输出。然而,RATs的反应机制尚未明确。在此,我们表明LMB和RAT A采用相同的分子机制使CRM1失活。CRM1第528位半胱氨酸残基的烷基化决定了对LMB和RATs的敏感性,并阻止CRM1货物蛋白的核输出。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验