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通过鸡脑微管相关蛋白2(MAP2):微管蛋白微管的拆解来测定磷酸雌莫司汀与MAP2结合的化学计量学。

Stoichiometry of estramustine phosphate binding to MAP2 measured by the disassembly of chick brain MAP2:tubulin microtubules.

作者信息

Burns R G

机构信息

Biophysics Section, Blackett Laboratory, Imperial College of Science, Technology and Medicine, London, England.

出版信息

Cell Motil Cytoskeleton. 1990;17(3):167-73. doi: 10.1002/cm.970170304.

Abstract

The concentration of estramustine phosphate required to inhibit the assembly or to induce the disassembly of chick brain MAP2:tubulin microtubules is markedly dependent upon the microtubule protein concentration. Analysis of this relationship shows that estramustine phosphate and tubulin compete for common MAP2 sites, that MAP2 can bind 5-6 moles.mole-1 estramustine phosphate, and that the Kd of these sites is congruent to 20 microM estramustine phosphate. It is proposed that two molecules of estramustine phosphate interact with each of the three tubulin-binding sites of MAP2 and inhibit the MAP2:tubulin interaction by neutralising two highly conserved basic residues.

摘要

抑制鸡脑微管相关蛋白2(MAP2)与微管蛋白组装或诱导其解聚所需的磷酸雌莫司汀浓度显著依赖于微管蛋白浓度。对这种关系的分析表明,磷酸雌莫司汀和微管蛋白竞争共同的MAP2位点,MAP2可结合5 - 6摩尔·摩尔⁻¹的磷酸雌莫司汀,且这些位点的解离常数(Kd)等同于20微摩尔的磷酸雌莫司汀。有人提出,两分子的磷酸雌莫司汀与MAP2的三个微管蛋白结合位点中的每一个相互作用,并通过中和两个高度保守的碱性残基来抑制MAP2与微管蛋白的相互作用。

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