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隐藻素1与微管蛋白和微管的相互作用。

Interaction of cryptophycin 1 with tubulin and microtubules.

作者信息

Kerksiek K, Mejillano M R, Schwartz R E, Georg G I, Himes R H

机构信息

Department of Biochemistry, University of Kansas, Lawrence 66045, USA.

出版信息

FEBS Lett. 1995 Dec 11;377(1):59-61. doi: 10.1016/0014-5793(95)01271-0.

Abstract

The cryptophycins are newly discovered antimitotic agents isolated from the cyanobacterium Nostoc. Previous studies using cultured cells demonstrated that microtubules are the target of these compounds. We have studied the interaction of cryptophycin 1 with tubulin and microtubules in vitro. Cryptophycin 1 is an effective inhibitor of tubulin polymerization, causes tubulin to aggregate, and depolymerizes microtubules to linear polymers somewhat similar to the spiral-like structures produced by the Vinca alkaloids. Cryptophycin 1 also inhibits vinblastine binding to tubulin but not colchicine binding. Thus, it appears that the cryptophycins may bind to the Vinca site in tubulin or to a site that overlaps with the Vinca site.

摘要

隐藻素是从蓝细菌念珠藻中分离出的新发现的抗有丝分裂剂。先前使用培养细胞的研究表明,微管是这些化合物的作用靶点。我们已经在体外研究了隐藻素1与微管蛋白和微管的相互作用。隐藻素1是微管蛋白聚合的有效抑制剂,可使微管蛋白聚集,并使微管解聚为线性聚合物, somewhat similar to the spiral-like structures produced by the Vinca alkaloids.隐藻素1还抑制长春碱与微管蛋白的结合,但不抑制秋水仙碱的结合。因此,隐藻素似乎可能与微管蛋白中的长春花碱结合位点或与长春花碱结合位点重叠的位点结合。

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