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1型人类免疫缺陷病毒包膜糖蛋白120的酶联免疫测定法。

Enzyme-linked immunoassay for human immunodeficiency virus type 1 envelope glycoprotein 120.

作者信息

Gilbert M, Kirihara J, Mills J

机构信息

Division of Infectious Diseases, San Francisco General Hospital, California 94110-2897.

出版信息

J Clin Microbiol. 1991 Jan;29(1):142-7. doi: 10.1128/jcm.29.1.142-147.1991.

DOI:10.1128/jcm.29.1.142-147.1991
PMID:1993748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC269718/
Abstract

An enzyme-linked immunosorbent assay (ELISA) that can measure picogram quantities of human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein 120 (gp120) in cell culture medium or body fluids has been developed. Recombinant, soluble CD4 immobilized in microtiter trays was used to capture gp120, which was then detected with polyclonal sheep antibody to gp120 followed by biotinylated rabbit anti-sheep immunoglobulin G and an avidin-alkaline phosphatase indicator system. With a reference recombinant gp120, the assay showed a linear relationship between optical density and concentrations ranging from 60 to 6,000 pg/100-microliters well; precision of the assay varied with the concentrations and ranged from +/- 40% with amounts smaller than 200 pg to +/- 10% with amounts larger than 200 pg. In a group of coded samples containing 60 pg (approximately 10(7) molecules) of reference gp120, the assay correctly identified the samples as containing gp120 99% of the time, with no false-positive results recorded for blank samples. Recombinant gp120 prepared in another cell culture system demonstrated a binding coefficient 13-fold lower than that of reference gp120. Mixing standard amounts of reference gp120 with increasing concentrations of human sera reduced assay sensitivity, although the linear relationship between gp120 concentration and optical density remained. With this assay we were able to detect gp120 in HIV-1 suspensions prepared from cultured lymphoblastoid cells and in the sera of HIV-1-infected patients. This ELISA for gp120 should be useful for studying the biological role of gp120 in HIV infection.

摘要

已开发出一种酶联免疫吸附测定法(ELISA),可测量细胞培养基或体液中皮克级量的人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白120(gp120)。固定在微量滴定板中的重组可溶性CD4用于捕获gp120,然后用抗gp120的多克隆羊抗体进行检测,接着使用生物素化的兔抗羊免疫球蛋白G和抗生物素蛋白-碱性磷酸酶指示系统。使用参考重组gp120,该测定法显示光密度与浓度在60至6000 pg/100微升孔之间呈线性关系;该测定法的精密度随浓度变化,量小于200 pg时为±40%,量大于200 pg时为±10%。在一组含有60 pg(约10⁷个分子)参考gp120的编码样品中,该测定法99%的时间能正确鉴定样品含有gp120,空白样品未记录到假阳性结果。在另一种细胞培养系统中制备的重组gp120显示结合系数比参考gp120低13倍。将标准量的参考gp120与浓度不断增加的人血清混合会降低测定法的灵敏度,尽管gp120浓度与光密度之间的线性关系仍然存在。使用该测定法,我们能够检测从培养的淋巴母细胞制备的HIV-1悬浮液以及HIV-1感染患者的血清中的gp120。这种用于gp120的ELISA对于研究gp120在HIV感染中的生物学作用应该是有用的。

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J Clin Microbiol. 1991 Jan;29(1):142-7. doi: 10.1128/jcm.29.1.142-147.1991.
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