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来自草履虫纤毛的22S、19S和12S动力蛋白的免疫学比较。

Immunological comparison of 22S, 19S, and 12S dyneins from Paramecium cilia.

作者信息

Walczak C E, Marchese-Ragona S P, Nelson D L

机构信息

Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison.

出版信息

Cell Motil Cytoskeleton. 1993;24(1):17-28. doi: 10.1002/cm.970240103.

Abstract

Three forms of dynein (22S, 19S, and 12S) were purified from Paramecium cilia. Two classes of monoclonal antibodies against purified 22S dynein were generated. One class reacted on immunoblots with the heavy chains of 22S, 19S, and 12S dyneins; the second class reacted with an 88 kD intermediate chain of 22S dynein. Polyclonal antiserum to the heavy chains of 22S dynein reacted with the alpha-heavy chain of 22S and 19S dyneins. A previously described antiserum raised against 22S dynein [Travis et al.: Biochim. Biophys. Acta 966:73-83, 1988] recognized the gamma-heavy chain of 22S dynein which was also present in 19S and 12S dyneins, along with the 88 and 76 kD intermediate chains of 22S dynein. This antiserum was also able to immunoprecipitate dynein from crude extracts of cilia. Electron microscopy revealed that the 22S dynein consisted mainly of two-headed particles with some three-headed particles present. The 12S dynein was mainly one-headed particles. The 19S dynein was a mixture of three-, two-, and one-headed particles. The immunological and electron microscopic studies showed that 19S dynein arises from 22S dynein, and that 12S dynein is heterogeneous, composed of the gamma-heavy chain of 22S dynein and a unique dynein ATPase. The polyclonal antibodies were also used to detect cross-reactive proteins in other organisms. Both the anti-heavy chain and the anti-22S dynein sera reacted strongly with 22S outer arm dynein of Tetrahymena, but not with the 14S dynein of this organism.

摘要

从草履虫纤毛中纯化出三种形式的动力蛋白(22S、19S和12S)。制备了两类针对纯化的22S动力蛋白的单克隆抗体。一类在免疫印迹上与22S、19S和12S动力蛋白的重链发生反应;另一类与22S动力蛋白的一条88 kD中间链发生反应。针对22S动力蛋白重链的多克隆抗血清与22S和19S动力蛋白的α-重链发生反应。一种先前描述的针对22S动力蛋白产生的抗血清[特拉维斯等人:生物化学与生物物理学报966:73 - 83,1988]识别22S动力蛋白的γ-重链,该重链也存在于19S和12S动力蛋白中,同时还识别22S动力蛋白的88和76 kD中间链。这种抗血清也能够从纤毛粗提物中免疫沉淀动力蛋白。电子显微镜显示,22S动力蛋白主要由双头颗粒组成,也有一些三头颗粒。12S动力蛋白主要是单头颗粒。19S动力蛋白是三头、双头和单头颗粒的混合物。免疫学和电子显微镜研究表明,19S动力蛋白源自22S动力蛋白,并且12S动力蛋白是异质的,由22S动力蛋白的γ-重链和一种独特的动力蛋白ATP酶组成。多克隆抗体还用于检测其他生物体中的交叉反应蛋白。抗重链血清和抗22S动力蛋白血清都与四膜虫的22S外臂动力蛋白强烈反应,但不与该生物体的14S动力蛋白反应。

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