Kaptein W A, Korf J, Cheng S, Yang M, Glatz J F, Renneberg R
Department of Chemistry, Hong Kong University of Science and Technology, Kowloon, China.
J Immunol Methods. 1998 Aug 1;217(1-2):103-11. doi: 10.1016/s0022-1759(98)00106-9.
In standard displacement flow immunoassays the analyte in the sample creates an active dissociation of labelled antigens (or antigen homologues) from an antigen binding site of an immobilized antibody, after which the labelled substance is measured downstream. Such systems have been described for molecules up to 1 kDa. In this study, we demonstrate displacement in a flow system for the detection of a small protein, cytoplasmic heart-type fatty acid-binding protein (15 kDa), a plasma marker for myocardial injury. The displacement system uses an inverse set-up: enzyme labelled monoclonal antibodies are associated to immobilized antigen, and are displaced by analyte in the sample. The system permits detection of both physiological (2-12 microg l(-1)) and pathological concentrations (12-2000 microg l(-1)) of fatty acid-binding protein in an on-line flow system.
在标准的置换流动免疫分析中,样品中的分析物会使标记抗原(或抗原类似物)从固定化抗体的抗原结合位点发生活性解离,之后在下游测量标记物质。这种系统已被描述用于检测分子量高达1 kDa的分子。在本研究中,我们展示了一种流动系统中的置换方法,用于检测一种小蛋白,即细胞质心脏型脂肪酸结合蛋白(15 kDa),它是心肌损伤的一种血浆标志物。该置换系统采用了一种反向设置:酶标记的单克隆抗体与固定化抗原结合,并被样品中的分析物置换。该系统能够在在线流动系统中检测脂肪酸结合蛋白的生理浓度(2 - 12 μg l⁻¹)和病理浓度(12 - 2000 μg l⁻¹)。