Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI, USA.
Methods Mol Biol. 2024;2829:277-286. doi: 10.1007/978-1-0716-3961-0_22.
Quantitative immunoassays, such as the traditional enzyme-linked immunosorbent assay (ELISA), are used to determine concentrations of an antigen in a matrix of unknown antigen concentration. Magnetic immunoassays, such as the Luminex xMAP technology, allow for the simultaneous detection of multiple analytes and offer heightened sensitivity, specificity, low sample volume requirements, and high-throughput capabilities. Here, we describe a quantitative immunoassay using the Luminex MAGPIX® System to determine the antigen concentration from liquid samples with unknown concentrations. In detail, we describe a newly developed assay for determining production yields of Drosophila S2-produced Marburg virus (MARV) glycoprotein in insect-cell-culture-derived supernatant. The potential applications of this assay could extend to the quantification of viral antigens in fluids derived from both in vitro and in vivo models infected with live MARV, thereby providing additional applications for virological research.
定量免疫分析,如传统的酶联免疫吸附测定(ELISA),用于测定未知抗原浓度基质中抗原的浓度。磁性免疫分析,如 Luminex xMAP 技术,允许同时检测多个分析物,并提供更高的灵敏度、特异性、低样品体积要求和高通量能力。在这里,我们描述了一种使用 Luminex MAGPIX®系统的定量免疫分析方法,用于确定具有未知浓度的液体样品中的抗原浓度。具体来说,我们描述了一种新开发的测定方法,用于测定昆虫细胞培养上清液中由 Drosophila S2 产生的马尔堡病毒(MARV)糖蛋白的产生产量。该测定方法的潜在应用可以扩展到定量来自感染活 MARV 的体外和体内模型的液体中的病毒抗原,从而为病毒学研究提供更多的应用。