水两相系统使均质免疫测定的多路复用。

Arlyne B Simon, John P Frampton, Nien-Tsu Huang, Katsuo Kurabayashi, Sophie Paczesny, Shuichi Takayama
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引用次数: 19

摘要

蛋白质生物标志物的定量测量对于生物标志物验证和早期疾病检测至关重要。目前的多重免疫测定既耗时又昂贵,而且准确度低。例如,多重elisa需要多个繁琐的洗涤和阻断步骤。此外,它们遭受非特异性抗体交叉反应,导致高背景和假阳性信号。在这里,我们展示了在水两相系统(ATPS)中共定位抗体-头对可以实现敏感,免洗,均质分析的多路复用,同时防止非特异性抗体交叉反应。我们的无交叉反应,多重检测可以同时检测细胞上清中四种蛋白质生物标志物((C-X-C基序)配体10 (CXCL10), CXCL9,白细胞介素(IL)-8和IL-6)的皮摩尔浓度。通过检测88例慢性移植物抗宿主病(GVHD)临床症状发作患者血浆中的诊断性生物标志物(CXCL10和CXCL9),证明了该检测方法的潜在临床实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Aqueous two-phase systems enable multiplexing of homogeneous immunoassays.

Quantitative measurement of protein biomarkers is critical for biomarker validation and early disease detection. Current multiplex immunoassays are time consuming costly and can suffer from low accuracy. For example, multiplex ELISAs require multiple, tedious, washing and blocking steps. Moreover, they suffer from nonspecific antibody cross-reactions, leading to high background and false-positive signals. Here, we show that co-localizing antibody-bead pairs in an aqueous two-phase system (ATPS) enables multiplexing of sensitive, no-wash, homogeneous assays, while preventing nonspecific antibody cross-reactions. Our cross-reaction-free, multiplex assay can simultaneously detect picomolar concentrations of four protein biomarkers ((C-X-C motif) ligand 10 (CXCL10), CXCL9, interleukin (IL)-8 and IL-6) in cell supernatants using a single assay well. The potential clinical utility of the assay is demonstrated by detecting diagnostic biomarkers (CXCL10 and CXCL9) in plasma from 88 patients at the onset of the clinical symptoms of chronic graft-versus-host disease (GVHD).

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TECHNOLOGY
TECHNOLOGY ENGINEERING, MULTIDISCIPLINARY-
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