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一种新型抗WIP单克隆抗体可检测到缺乏WASP结合结构域的WIP异构体。

A novel anti-WIP monoclonal antibody detects an isoform of WIP that lacks the WASP binding domain.

作者信息

Koduru Suresh, Massaad Michel, Wilbur Christopher, Kumar Lalit, Geha Raif, Ramesh Narayanaswamy

机构信息

Division of Immunology, Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Biochem Biophys Res Commun. 2007 Feb 23;353(4):875-81. doi: 10.1016/j.bbrc.2006.12.079. Epub 2006 Dec 20.

Abstract

The majority of Wiskott-Aldrich syndrome protein (WASP) in T cells is in a complex with WASP interacting protein (WIP), a 503 a.a. long proline rich protein. Here we demonstrate that a novel anti-WIP mAb, 3D10, recognizes an epitope in the N-terminal domain of the WIP protein, within the sequence 13PTFALA18. mAb 3D10 competes with actin, but not with WASP or Nck, for WIP binding. Analysis of 3D10 immunoprecipitates failed to demonstrate dissociation of the WASP-WIP complex after TCR ligation that we previously reported using a polyclonal anti-WIP anti-serum raised against a C-terminal peptide (a.a. 459-503) that spanned the WASP binding site. 3D10 mAb allowed the detection of a novel isoform of WIP consisting of a truncated 403 a.a. long protein that includes the 377 a.a. encoded by the first 4 exons of WIP followed by a 26 a.a. sequence encoded by intron 4.

摘要

T细胞中大多数威斯科特-奥尔德里奇综合征蛋白(WASP)与WASP相互作用蛋白(WIP)形成复合物,WIP是一种富含脯氨酸的503个氨基酸长的蛋白质。在此我们证明,一种新型抗WIP单克隆抗体3D10识别WIP蛋白N端结构域中13PTFALA18序列内的一个表位。单克隆抗体3D10与肌动蛋白竞争WIP的结合,但不与WASP或Nck竞争。对3D10免疫沉淀产物的分析未能证明在TCR连接后WASP-WIP复合物发生解离,而我们之前使用针对跨越WASP结合位点的C端肽(氨基酸459 - 503)产生的多克隆抗WIP抗血清报道过这种解离现象。3D10单克隆抗体能够检测到一种新型WIP异构体,其为截短的403个氨基酸长的蛋白质,包括由WIP前4个外显子编码的377个氨基酸,接着是由内含子4编码的26个氨基酸序列。

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