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培养的非神经元细胞中的一种205 kDa蛋白质含有微管蛋白结合表位。

A 205 kDa protein from non-neuronal cells in culture contains tubulin binding epitopes.

作者信息

Vial C, Armas-Portela R, Avila J, González M, Maccioni R B

机构信息

International Center for Cancer and Developmental Biology (ICC), University of Chile, Santiago.

出版信息

Mol Cell Biochem. 1995 Mar 23;144(2):109-116. doi: 10.1007/BF00944389.

Abstract

Microtubule-associated proteins (MAPs) interact with tubulin in vitro and in vivo. Despite that there is a large amount of information on the roles of these proteins in neurons, the data on non-neuronal MAPs or MAPs-related proteins is scarce. There is an increasing number of microtubule-interacting proteins that have been identified in different cultured cell lines, and some of them share common functional epitopes with the most well-known MAPs, MAP-2 and tau. In a search for tubulin-interacting proteins in non-neuronal cells we identified a 205 kDa protein in the monkey kidney Vero cells in culture, on the basis of immunological studies and affinity chromatography. This protein interacts with the C-terminal moiety of beta-tubulin and cosediments with taxol assembled microtubules, but it was not recovered after successive cycles of assembly and disassembly. The presence of neuronal MAPs such as MAP-1, MAP-2 and tau was not detected in these cells. Interestingly, the studies showed that the 205 kDa protein contained a tubulin binding motif which was recognized by site-directed antibodies that also tag tubulin binding epitopes on MAP-2 and tau. This characteristic led us to designate this protein as MBD-205, a component that shares binding domains with these MAPs, rather than as a marker of the MAPs family. On the other hand, immunofluorescence experiments using site-specific antibodies, i.e. MAP-reacting monoclonal anti-idiotypic reagent MTB6.22 and a polyclonal antibody to the second tau repeat, revealed a MBD-205 co-localization with membrane structures and microtubule-organizing centers in Vero cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

微管相关蛋白(MAPs)在体内外均能与微管蛋白相互作用。尽管关于这些蛋白在神经元中的作用已有大量信息,但关于非神经元MAPs或MAPs相关蛋白的数据却很稀少。在不同的培养细胞系中,已鉴定出越来越多的微管相互作用蛋白,其中一些与最著名的MAPs(MAP - 2和tau)具有共同的功能表位。在寻找非神经元细胞中的微管蛋白相互作用蛋白时,我们基于免疫学研究和亲和层析,在培养的猴肾Vero细胞中鉴定出一种205 kDa的蛋白。该蛋白与β-微管蛋白的C末端部分相互作用,并与紫杉醇组装的微管共沉降,但在连续的组装和拆卸循环后未被回收。在这些细胞中未检测到神经元MAPs如MAP - 1、MAP - 2和tau的存在。有趣的是,研究表明,205 kDa的蛋白含有一个微管蛋白结合基序,该基序可被定点抗体识别,这些抗体也标记MAP - 2和tau上的微管蛋白结合表位。这一特性使我们将该蛋白命名为MBD - 205,它是一种与这些MAPs共享结合域的成分,而不是MAPs家族的标志物。另一方面,使用位点特异性抗体(即与MAP反应的单克隆抗独特型试剂MTB6.22和针对tau第二个重复序列的多克隆抗体)进行的免疫荧光实验显示,MBD - 205与Vero细胞中的膜结构和微管组织中心共定位。(摘要截短于250字)

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