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组织培养细胞中Z-DNA结合蛋白的检测

Detection of Z DNA binding proteins in tissue culture cells.

作者信息

Leith I R, Hay R T, Russell W C

机构信息

Department of Biochemistry and Microbiology, University of St Andrews, Fife, UK.

出版信息

Nucleic Acids Res. 1988 Sep 12;16(17):8277-89. doi: 10.1093/nar/16.17.8277.

Abstract

A gel electrophoresis DNA binding assay to detect Z DNA binding proteins has been developed utilising [32P] labelled poly [d(G-C)] which was converted to the Z form by incubation in 100 microM Co(NH3)6Cl3. The parameters of the assay were established using a Z DNA antibody as a model system and then applied to extracts of Hela and BHK21 cells. Using an anti-Z DNA antibody conditions were established which allowed resolution of antibody-DNA complexes and free DNA in the presence of 100 microM Co(NH3)6Cl3. The inclusion of unlabelled complementary homopolymers eliminated non-specific binding to the labelled Z-DNA probe. Competition experiments demonstrated that the assay was highly specific for double stranded non-B DNA. Application of the technique to extracts of mammalian cells demonstrated that human and hamster cells contain Z-DNA binding proteins; further characterisation by a blotting technique indicated that a 56,000 molecular weight cell protein preferentially binds Z-DNA.

摘要

利用[32P]标记的聚[d(G-C)]开发了一种凝胶电泳DNA结合测定法,用于检测Z-DNA结合蛋白,该聚[d(G-C)]通过在100微摩尔Co(NH3)6Cl3中孵育转化为Z型。使用Z-DNA抗体作为模型系统建立了测定参数,然后应用于Hela和BHK21细胞提取物。使用抗Z-DNA抗体建立了条件,使得在100微摩尔Co(NH3)6Cl3存在下能够分辨抗体-DNA复合物和游离DNA。加入未标记的互补同聚物消除了与标记的Z-DNA探针的非特异性结合。竞争实验表明该测定法对双链非B-DNA具有高度特异性。将该技术应用于哺乳动物细胞提取物表明人和仓鼠细胞含有Z-DNA结合蛋白;通过印迹技术进一步表征表明一种分子量为56,000的细胞蛋白优先结合Z-DNA。

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