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夹心免疫分析法在血浆分泌组学中的系统开发

Systematic Development of Sandwich Immunoassays for the Plasma Secretome.

机构信息

Division of Affinity Proteomics, Science for Life Laboratory, KTH - Royal Institute of Technology, Box 1031, 171 21, Solna, Sweden.

Division of Cellular and Clinical Proteomics, Science for Life Laboratory, KTH - Royal Institute of Technology, Box 1031, 171 21, Solna, Sweden.

出版信息

Proteomics. 2019 Aug;19(15):e1900008. doi: 10.1002/pmic.201900008. Epub 2019 Jul 22.

Abstract

The plasma proteome offers a clinically useful window into human health. Recent advances from highly multiplexed assays now call for appropriate pipelines to validate individual candidates. Here, a workflow is developed to build dual binder sandwich immunoassays (SIA) and for proteins predicted to be secreted into plasma. Utilizing suspension bead arrays, ≈1800 unique antibody pairs are first screened against 209 proteins with recombinant proteins as well as EDTA plasma. Employing 624 unique antibodies, dilution-dependent curves in plasma and concentration-dependent curves of full-length proteins for 102 (49%) of the targets are obtained. For 22 protein assays, the longitudinal, interindividual, and technical performance is determined in a set of plasma samples collected from 18 healthy subjects every third month over 1 year. Finally, 14 of these assays are compared with with SIAs composed of other binders, proximity extension assays, and affinity-free targeted mass spectrometry. The workflow provides a multiplexed approach to screen for SIA pairs that suggests using at least three antibodies per target. This design is applicable for a wider range of targets of the plasma proteome, and the assays can be applied for discovery but also to validate emerging candidates derived from other platforms.

摘要

血浆蛋白质组为了解人类健康提供了一个具有临床应用价值的窗口。目前,高通量检测技术的发展要求建立适当的流程来验证单个候选物。在这里,开发了一种工作流程来构建双结合物夹心免疫分析(SIA)和预测分泌到血浆中的蛋白质。利用悬浮珠阵列,首先用重组蛋白和 EDTA 血浆筛选了约 1800 对独特的抗体对 209 种蛋白质。使用 624 对独特的抗体,获得了 102 个(49%)目标物的血浆中稀释依赖性曲线和全长蛋白质浓度依赖性曲线。对于 22 个蛋白质检测,在从 18 名健康受试者收集的一组血浆样本中,每三个月收集一次,共收集一年,确定了这些检测的纵向、个体间和技术性能。最后,将其中 14 种检测与由其他结合物、邻近延伸检测和无亲和力靶向质谱法组成的 SIA 进行了比较。该工作流程提供了一种用于筛选 SIA 对的高通量方法,建议每个靶标使用至少三种抗体。这种设计适用于更广泛的血浆蛋白质组靶标,并且可以用于发现,也可以用于验证来自其他平台的新兴候选物。

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