首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Monoclonal antibody identification of a 100-kDa membrane protein in HeLa cells and human spinal cord involved in poliovirus attachment.
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Monoclonal antibody identification of a 100-kDa membrane protein in HeLa cells and human spinal cord involved in poliovirus attachment.

机译:涉及脊髓灰质炎病毒附着的HeLa细胞和人脊髓中100 kDa膜蛋白的单克隆抗体鉴定。

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摘要

Unique receptor sites for poliovirus are considered to be the primary determinant of the virus' cell and tissue-type specificity. To study the poliovirus-cell interaction, eight monoclonal antibodies that specifically block the cytopathic effects of poliovirus were generated by using HeLa cell preparations as immunogen and a newly developed colorimetric screening assay. Plaque-inhibition assays confirmed the viral specificity of the antibodies, and when one antibody, AF3, was used as a probe in immunoblots of cell membrane preparations, it detected a 100-kDa band in only those cell lines and tissues permissive for poliovirus infection. AF3 also specifically inhibited radiolabeled poliovirus binding to cells. In terms of tissue specificity, AF3 detected the 100-kDa band in membrane preparations from human spinal cord but not in organ homogenates of human kidney or in murine tissue, including the central nervous system. Furthermore, AF3 detected the band in a human-mouse hybrid cell line containing human chromosome 19, which confers permissivity for poliovirus infection, but the antibody did not detect the band in a human chromosome 19-deficient subclone. In an immunohistochemical study of the human brainstem, AF3 stained neurons in the reticular formation and clusters of brainstem neurons, consistent with the known pattern of damage caused by poliovirus infection in the brainstem. Furthermore, AF3 reacted with human peripheral mononuclear cells, consistent with the known replication of poliovirus in Peyer's patches and tonsils. These results strongly suggest that the 100-kDa band detected by antibody AF3 is, or is closely associated with, the poliovirus receptor site.
机译:脊髓灰质炎病毒的独特受体位点被认为是病毒细胞和组织类型特异性的主要决定因素。为了研究脊髓灰质炎病毒与细胞的相互作用,通过使用HeLa细胞制备物作为免疫原和新开发的比色筛选测定法,产生了八种特异性阻断脊髓灰质炎病毒的细胞病变作用的单克隆抗体。噬菌斑抑制测定法证实了抗体的病毒特异性,当一种抗体AF3作为细胞膜制剂免疫印迹的探针时,它仅在允许脊髓灰质炎病毒感染的那些细胞系和组织中检测到100 kDa的条带。 AF3还特异性抑制放射性标记的脊髓灰质炎病毒与细胞结合。就组织特异性而言,AF3在人脊髓膜制剂中检测到100 kDa条带,但在人肾器官匀浆或鼠组织(包括中枢神经系统)中未检测到。此外,AF3在含有人染色体19的人鼠杂交细胞系中检测到该条带,从而赋予了脊髓灰质炎病毒感染的许可性,但该抗体未在人染色体19缺陷型亚克隆中检测到该条带。在对人脑干的免疫组织化学研究中,AF3对网状结构和脑干神经元簇中的神经元进行了染色,这与脑干中脊髓灰质炎病毒感染引起的已知损伤方式一致。此外,AF3与人外周单核细胞反应,这与脊髓灰质炎病毒在派伊尔氏淋巴结和扁桃体中的已知复制相一致。这些结果有力地表明,由抗体AF3检测到的100-kDa带是脊髓灰质炎病毒受体位点,或与其紧密相关。

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