Suppr超能文献

依托匹可硫酸钠激活微管蛋白结合的结构基础。

Structural Basis of Noscapine Activation for Tubulin Binding.

机构信息

Centro de Investigaciones Biológicas Margarita Salas-CSIC, Ramiro de Maeztu, 9, C.P. 28040 Madrid, Spain.

Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland.

出版信息

J Med Chem. 2020 Aug 13;63(15):8495-8501. doi: 10.1021/acs.jmedchem.0c00855. Epub 2020 Jul 29.

Abstract

Noscapine is a natural alkaloid that is used as an antitussive medicine. However, it also acts as a weak anticancer agent in certain models through a mechanism that is largely unknown. Here, we performed structural studies and show that the cytotoxic agent 7A--demethoxy-amino-noscapine (7A-aminonoscapine) binds to the colchicine site of tubulin. We suggest that the 7A-methoxy group of noscapine prevents binding to tubulin due to a steric clash of the compound with the T5-loop of α-tubulin. We further propose that the anticancer activity of noscapine arises from a bioactive metabolite that binds to the colchicine site of tubulin to induce mitotic arrest through a microtubule cytoskeleton-based mechanism.

摘要

那可丁是一种天然生物碱,用作镇咳药。然而,在某些模型中,它也作为一种弱抗癌剂发挥作用,其机制在很大程度上尚不清楚。在这里,我们进行了结构研究,表明细胞毒性剂 7A--去甲氧基-氨基那可丁(7A-氨基那可丁)与微管蛋白的秋水仙碱结合位点结合。我们认为那可丁的 7A-甲氧基基团由于化合物与 α-微管蛋白的 T5-环的空间位阻而阻止与微管蛋白结合。我们进一步提出,那可丁的抗癌活性来自于一种生物活性代谢物,该代谢物与微管蛋白的秋水仙碱结合位点结合,通过基于微管细胞骨架的机制诱导有丝分裂停滞。

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