McDonald Jacqueline U, Ekeruche-Makinde Julia, Ho Mei M, Tregoning John S, Ashiru Omodele
Mucosal Infection & Immunity Group, Section of Virology, Imperial College London, St Mary's Campus, London W2 1PG, United Kingdom.
Mucosal Infection & Immunity Group, Section of Virology, Imperial College London, St Mary's Campus, London W2 1PG, United Kingdom.
J Immunol Methods. 2016 Jun;433:6-16. doi: 10.1016/j.jim.2016.02.018. Epub 2016 Feb 24.
Multiplex bead-based assays have many advantages over ELISA, particularly for the analyses of large quantities of samples and/or precious samples of limited volume. Although many commercial arrays covering multitudes of biologically significant analytes are available, occasionally the development of custom arrays is necessary. Here, the development of a custom pentaplex sandwich immunoassay using Protein G-coupled beads, for analysis using the Luminex® xMAP® platform, is described. This array was required for the measurement of candidate biomarkers of vaccine safety in small volumes of mouse sera. Optimisation of this assay required a stepwise approach: testing cross-reactivity of the antibody pairs, the development of an in-house serum diluent buffer as well as heat-inactivation of serum samples to prevent interference from matrix effects. We then demonstrate the use of this array to analyse inflammatory mediators in mouse serum after immunisation. The work described here exemplifies how Protein G-coupled beads offer a flexible and robust approach to develop custom multiplex immunoassays, which can be applied to a range of analytes from multiple species.
基于微珠的多重检测法相对于酶联免疫吸附测定(ELISA)具有许多优势,特别是在分析大量样本和/或少量珍贵样本时。尽管有许多涵盖多种具有生物学意义分析物的商业阵列可供使用,但有时仍需要开发定制阵列。在此,描述了一种使用与蛋白G偶联的微珠开发的定制五重夹心免疫测定法,用于使用Luminex® xMAP®平台进行分析。该阵列用于测量少量小鼠血清中疫苗安全性的候选生物标志物。该检测法的优化需要逐步进行:测试抗体对的交叉反应性,开发内部血清稀释缓冲液以及对血清样本进行热灭活以防止基质效应的干扰。然后,我们展示了该阵列在分析免疫后小鼠血清中的炎症介质方面的应用。此处描述的工作例证了与蛋白G偶联的微珠如何提供一种灵活且强大的方法来开发定制的多重免疫测定法,该方法可应用于来自多个物种的一系列分析物。