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跨越tau分子的表位与双螺旋丝共享。

Epitopes that span the tau molecule are shared with paired helical filaments.

作者信息

Kosik K S, Orecchio L D, Binder L, Trojanowski J Q, Lee V M, Lee G

机构信息

Center for Neurologic Diseases, Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

Neuron. 1988 Nov;1(9):817-25. doi: 10.1016/0896-6273(88)90129-8.

Abstract

Tau protein has been shown to be an integral component of Alzheimer paired helical filaments (PHF). However, the extent to which tau is incorporated into PHF has not been clear because the antibodies used to label PHF generally do not have precisely defined epitopes. Here we define the antigenic sites for five monoclonal antibodies that react with tau and cross-react with SDS-extracted neurofibrillary tangles. The reactive sites were determined by screening a lambda gt11 sublibrary expressing small fragments of the tau sequence. The mapped epitopes were found to span almost the entire length of tau, suggesting that PHF contains tau in its entirety or nearly in its entirety. One antibody was found to cross-react with microtubule-associated protein 2, implying some degree of homology between the two proteins.

摘要

已证明tau蛋白是阿尔茨海默病成对螺旋丝(PHF)的一个重要组成部分。然而,由于用于标记PHF的抗体通常没有精确界定的表位,tau蛋白整合到PHF中的程度尚不清楚。在此,我们确定了五种与tau反应并与十二烷基硫酸钠(SDS)提取的神经原纤维缠结发生交叉反应的单克隆抗体的抗原位点。通过筛选表达tau序列小片段的λgt11亚文库来确定反应位点。所绘制的表位几乎跨越了tau的整个长度,这表明PHF包含完整或几乎完整的tau。发现一种抗体与微管相关蛋白2发生交叉反应,这意味着这两种蛋白之间存在一定程度的同源性。

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