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针对呼吸道合胞病毒蛋白的单克隆抗体:融合蛋白的鉴定

Monoclonal antibodies to respiratory syncytial virus proteins: identification of the fusion protein.

作者信息

Walsh E E, Hruska J

出版信息

J Virol. 1983 Jul;47(1):171-7. doi: 10.1128/JVI.47.1.171-177.1983.

Abstract

Six monoclonal antibodies directed against respiratory syncytial virus proteins were produced. Each was characterized by immunoprecipitation and indirect immunofluorescence. One was directed against the nucleocapsid protein. NP 44, two were directed against a 37,000-dalton protein, two were directed against the major envelope glycoprotein, GP 90, and one was directed against the 70,000-dalton envelope protein, VP 70. Indirect immunofluorescence stain patterns of infected HEp-2 cells defined GP 90 and VP 70 as viral proteins expressed on the cell surface, whereas NP 44 and the 37,000-dalton protein were detected as intracytoplasmic inclusions. One of the anti-GP 90 antibodies neutralized virus only in the presence of complement but did not inhibit cell-cell fusion. The anti-VP 70 antibody neutralized virus without complement and inhibited cell-cell fusion of previously infected HEp-2 cells, thus identifying VP 70 as the fusion protein.

摘要

制备了六种针对呼吸道合胞病毒蛋白的单克隆抗体。每种抗体都通过免疫沉淀和间接免疫荧光进行了表征。一种针对核衣壳蛋白NP 44,两种针对一种37000道尔顿的蛋白,两种针对主要包膜糖蛋白GP 90,一种针对70000道尔顿的包膜蛋白VP 70。感染的HEp-2细胞的间接免疫荧光染色模式将GP 90和VP 70定义为在细胞表面表达的病毒蛋白,而NP 44和37000道尔顿的蛋白则被检测为胞质内包涵体。其中一种抗GP 90抗体仅在补体存在的情况下中和病毒,但不抑制细胞间融合。抗VP 70抗体在没有补体的情况下中和病毒,并抑制先前感染的HEp-2细胞的细胞间融合,从而将VP 70鉴定为融合蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d104/255221/dfdc8f18a4f3/jvirol00142-0181-a.jpg

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