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[一种新型蛋白质,类CAR可溶性蛋白(CLSP)在腺病毒感染中的作用]

[Role of a novel protein, CAR-like soluble protein (CLSP), in adenovirus infection].

作者信息

Kawabata Kenji

机构信息

Laboratory of Gene Transfer and Regulation, National Institute of Biomedical Innovation, Osaka, Japan.

出版信息

Yakugaku Zasshi. 2007 Jul;127(7):1091-6. doi: 10.1248/yakushi.127.1091.

Abstract

Coxsackievirus and adenovirus receptor (CAR) is a member of the immunoglobulin superfamily and a component of epithelial tight junction. CAR also functions as a primary receptor for coxsackievirus B and adenovirus (Ad) infection. Recently, we have identified a novel protein, CAR-like soluble protein (CLSP), which is closely related to CAR. Mouse CLSP (mCLSP) was composed of 390 amino acids, including three Ig domains, and showed strong homology to the IgV domain of CAR. Interestingly, mCLSP lacks a transmembrane domain, indicating that this is a soluble protein. When mCLSP cDNA was introduced into CAR-positive cells, the infection with Ad vector was severely inhibited. On the other hand, mCLSP promoted the infection with Ad vector in CAR-negative cells. Furthermore, recombinant CLSP directly bound to Ad and inhibited the Ad vector-mediated transduction in CAR-positive cells. Computational analysis for a genome database showed that the CLSP gene is rodent-specific, and that human and bovine lack this gene. Here, I discuss the function of CLSP for Ad infection.

摘要

柯萨奇病毒和腺病毒受体(CAR)是免疫球蛋白超家族的成员,也是上皮紧密连接的一个组成部分。CAR还是柯萨奇病毒B和腺病毒(Ad)感染的主要受体。最近,我们鉴定出一种新型蛋白质,即CAR样可溶性蛋白(CLSP),它与CAR密切相关。小鼠CLSP(mCLSP)由390个氨基酸组成,包括三个免疫球蛋白结构域,并且与CAR的免疫球蛋白V结构域具有高度同源性。有趣的是,mCLSP缺乏跨膜结构域,这表明它是一种可溶性蛋白。当将mCLSP cDNA导入CAR阳性细胞时,腺病毒载体的感染受到严重抑制。另一方面,mCLSP促进了腺病毒载体在CAR阴性细胞中的感染。此外,重组CLSP直接与腺病毒结合,并抑制腺病毒载体介导的CAR阳性细胞转导。对基因组数据库的计算分析表明,CLSP基因是啮齿动物特有的,人和牛没有该基因。在此,我将讨论CLSP在腺病毒感染中的作用。

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