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能区分多瘤病毒中T抗原对pp60c-src或蛋白磷酸酶2A结合情况的新型单克隆抗体。

Novel monoclonal antibodies that differentiate between the binding of pp60c-src or protein phosphatase 2A by polyomavirus middle T antigen.

作者信息

Dilworth S M, Horner V P

机构信息

Department of Chemical Pathology, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.

出版信息

J Virol. 1993 Apr;67(4):2235-44. doi: 10.1128/JVI.67.4.2235-2244.1993.

Abstract

Fourteen pGEX plasmids that express defined regions of polyomavirus middle T antigen in bacteria have been constructed. These polypeptides have been used to generate 18 new monoclonal antibodies directed against the unique portion of middle T and to map the approximate position of the antibody recognition sites onto the protein sequence. All of the antibodies effectively immunoprecipitate middle T and the associated 60- and 35-kDa components of protein phosphatase 2A. Four of the antibodies, however, do not react with middle T when it is bound to pp60c-src. These four probably bind to amino acids 203 to 218 of the middle T protein sequence, which are encoded by the mRNA immediately 3' to the splice junction that creates the C-terminal unique region. This suggests that additional middle T sequences are required for middle T's interaction with pp60c-src than are needed for its binding to protein phosphatase 2A. The antibodies localize this extra region and provide a means of distinguishing between these two associations.

摘要

已构建了14种在细菌中表达多瘤病毒中T抗原特定区域的pGEX质粒。这些多肽已用于产生18种针对中T独特部分的新单克隆抗体,并将抗体识别位点的大致位置定位到蛋白质序列上。所有抗体均能有效免疫沉淀中T以及蛋白磷酸酶2A的相关60 kDa和35 kDa成分。然而,其中四种抗体在中T与pp60c-src结合时不与之反应。这四种抗体可能与中T蛋白序列的第203至218位氨基酸结合,这些氨基酸由紧接在产生C末端独特区域的剪接连接处3'端的mRNA编码。这表明中T与pp60c-src相互作用所需的中T序列比其与蛋白磷酸酶2A结合所需的序列更多。这些抗体定位了这个额外区域,并提供了区分这两种结合的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b58/240352/c2652db19f81/jvirol00025-0505-a.jpg

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