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重组驱动蛋白运动结构域与β-微管蛋白结合,并以B表面晶格装饰微管。

Recombinant kinesin motor domain binds to beta-tubulin and decorates microtubules with a B surface lattice.

作者信息

Song Y H, Mandelkow E

机构信息

Max Planck Unit for Structural Molecular Biology, Deutsches Elektronen Synchrotron, Hamburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1671-5. doi: 10.1073/pnas.90.5.1671.

Abstract

We have expressed the recombinant squid kinesin head domain in Escherichia coli and studied its interaction with microtubules. The head is active as a microtubule-stimulated ATPase and binds to microtubules, but it does not support microtubule gliding by itself. The head binds to both microtubules and depolymerized tubulin. In each case the zero-length crosslinker 1-ethyl-3-[3-dimethylamino)propyl] carbodiimide induces a bond specifically to beta- but not alpha-tubulin. The head decorates brain microtubules with an 8-nm axial spacing. Thus the stoichiometry is one kinesin head per tubulin dimer. The lattice is that of flagellar B-tubules, implying that reassembled microtubules are not symmetric. Moreover, the A- and B-tubules of intact flagellar outer doublets are both decorated with a B lattice. This suggests that the B lattice is a general property of microtubules.

摘要

我们已在大肠杆菌中表达了重组鱿鱼驱动蛋白头部结构域,并研究了其与微管的相互作用。该头部作为微管刺激的ATP酶具有活性,并能与微管结合,但它自身并不支持微管滑动。该头部能与微管和去聚合的微管蛋白结合。在每种情况下,零长度交联剂1-乙基-3-[3-二甲基氨基)丙基]碳二亚胺都会特异性地诱导与β-微管蛋白而非α-微管蛋白形成键。该头部以8纳米的轴向间距装饰脑微管。因此,化学计量比是每微管蛋白二聚体有一个驱动蛋白头部。晶格是鞭毛B微管的晶格,这意味着重新组装的微管不对称。此外,完整鞭毛外双联微管的A微管和B微管都被B晶格装饰。这表明B晶格是微管的一个普遍特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d697/45941/82c7c342967b/pnas01464-0047-a.jpg

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