首页> 美国卫生研究院文献>Journal of Virology >Plasma membrane orientation of simian virus 40 T antigen in three transformed cell lines mapped with monoclonal antibodies.
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Plasma membrane orientation of simian virus 40 T antigen in three transformed cell lines mapped with monoclonal antibodies.

机译:猿猴病毒40 T抗原在用单克隆抗体作图的三个转化细胞系中的质膜取向。

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摘要

Simian virus 40 large T antigen transforms cells from several species. Recent studies show that it is present on the cell surface. As in other tumor virus systems, this may be important for transformation. We have used a radioimmunoassay to map antigenic determinants on living and formaldehyde-fixed transformed cells with six different monoclonal antibodies to T antigen. Nonrelevant monoclonal antibodies of the same subclasses served as controls. With the transformed mouse line SVT2, antibody PAb 101, which reacts with the C-terminal region of T antigen, and PAb 1700, which is directed against an internal region of T, reacted with both formaldehyde-fixed and living cells. Antibodies PAb 402 (C terminus) and 419 (N terminus) reacted only with living cells, their determinants being destroyed upon formaldehyde fixation. Antibodies PAb 405 (C terminus) and 100 (internal) fail to react on either fixed or living cells. Similar results were obtained on the simian virus 40-transformed human line SV80 and the fixed hamster line CHLwt23, although all antibodies failed to react with living CHLwt23 cells. The data suggest that T antigen is inserted into the plasma membrane of transformed cells in a specific, nonrandom manner, with the C and N termini exposed on the cell surface and the midportion either buried in the lipid bilayer, hidden by the tertiary structure of T antigen, or masked by a post-translational modification such as fatty acid acylation.
机译:猿猴病毒40大T抗原可转化几种物种的细胞。最近的研究表明它存在于细胞表面。像在其他肿瘤病毒系统中一样,这对于转化可能很重要。我们已经使用放射免疫分析法在活体和甲醛固定的转化细胞上绘制了抗原决定簇,其中有六种不同的针对T抗原的单克隆抗体。相同亚类的非相关单克隆抗体用作对照。使用转化的小鼠品系SVT2,与T抗原的C端区域反应的抗体PAb 101和针对T的内部区域的PAb 1700与固定甲醛的细胞和活细胞反应。抗体PAb 402(C端)和419(N端)仅与活细胞反应,其决定簇在甲醛固定后被破坏。抗体PAb 405(C末端)和100(内部)无法在固定细胞或活细胞上反应。尽管所有抗体都无法与活的CHLwt23细胞反应,但在猿猴病毒40转化的人SV80系和固定仓鼠系CHLwt23上也获得了相似的结果。数据表明,T抗原以特定的,非随机的方式插入转化细胞的质膜中,C和N末端暴露在细胞表面,中部埋在脂质双层中,被T的三级结构隐藏抗原,或被翻译后修饰(例如脂肪酸酰化)掩盖。

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