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利用单克隆抗体Mab 34-23鉴定人嗜T淋巴细胞病毒I型(HTLV-I)的假定细胞受体。

Identification of a putative cellular receptor for HTLV-I by a monoclonal antibody, Mab 34-23.

作者信息

Gavalchin J, Fan N, Lane M J, Papsidero L, Poiesz B J

机构信息

Department of Medicine, SUNY Health Science Center, New York 13210.

出版信息

Virology. 1993 May;194(1):1-9. doi: 10.1006/viro.1993.1228.

Abstract

The ability of HTLV-I to infect cells is presumed to be dependent, in some part, on the attachment of the virus to a target cell via a specific cell surface receptor which is, as yet, unknown. Here we present evidence that a monoclonal antibody, Mab 34-23, inhibits the binding of HTLV-I to IL-2 and phytohemagglutinin-activated peripheral blood mononuclear cells and also inhibits virus entry into these cells. Analysis of a variety of target cells, including a human:mouse somatic hybrid which contains only human chromosome 17q, indicates that the binding of Mab 34-23 correlates with HTLV-I adsorption and entry. SDS-PAGE and Western blot analysis show that Mab 34-23 binds to four major proteins of MW 31, 45, 55, and 70 kDa and this binding can be inhibited by HTLV-I and not HIV proteins. HTLV-I virions bind to proteins of similar molecular weight and virus-binding to these proteins can be inhibited by preincubation with Mab 34-23. These data suggest that Mab 34-23 may identify a specific cell surface receptor(s) for HTLV-I.

摘要

人们推测,人嗜T淋巴细胞病毒I型(HTLV-I)感染细胞的能力在一定程度上取决于该病毒通过一种尚未明确的特定细胞表面受体与靶细胞的结合。在此,我们提供证据表明,单克隆抗体Mab 34-23可抑制HTLV-I与白细胞介素-2(IL-2)及植物血凝素激活的外周血单个核细胞的结合,还能抑制病毒进入这些细胞。对多种靶细胞的分析,包括仅含人类17号染色体q臂的人-鼠体细胞杂种,表明Mab 34-23的结合与HTLV-I的吸附及进入相关。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹分析显示,Mab 34-23与分子量分别为31、45、55和70 kDa的四种主要蛋白质结合,且这种结合可被HTLV-I而非HIV蛋白质抑制。HTLV-I病毒粒子与分子量相似的蛋白质结合,预先用Mab 34-23孵育可抑制病毒与这些蛋白质的结合。这些数据表明,Mab 34-23可能识别出HTLV-I的一种特定细胞表面受体。

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