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抗体 - 胸苷激酶1复合物的微芯片免疫亲和电泳

Microchip immunoaffinity electrophoresis of antibody-thymidine kinase 1 complex.

作者信息

Pagaduan Jayson V, Ramsden Madison, O'Neill Kim, Woolley Adam T

机构信息

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA.

出版信息

Electrophoresis. 2015 Mar;36(5):813-7. doi: 10.1002/elps.201400436. Epub 2015 Feb 3.

Abstract

Thymidine kinase 1 (TK1) is an important cancer biomarker whose serum levels are elevated in early cancer development. We developed a microchip electrophoresis immunoaffinity assay to measure recombinant purified TK1 (pTK1) using an antibody (Ab) that binds to human TK1. We fabricated PMMA microfluidic devices to test the feasibility of detecting Ab-pTK1 immune complexes as a step toward TK1 analysis in clinical serum samples. We were able to separate immune complexes from unbound Abs using 0.5× PBS (pH 7.4) containing 0.01% Tween-20, with 1% w/v methylcellulose that acts as a dynamic surface coating and sieving matrix. Separation of the Ab and Ab-pTK1 complex was observed within a 5 mm effective separation length. This method of detecting pTK1 is easy to perform, requires only a 10 μL sample volume, and takes just 1 min for separation.

摘要

胸苷激酶1(TK1)是一种重要的癌症生物标志物,其血清水平在癌症早期发展阶段会升高。我们开发了一种微芯片电泳免疫亲和测定法,使用与人TK1结合的抗体(Ab)来测量重组纯化的TK1(pTK1)。我们制造了聚甲基丙烯酸甲酯(PMMA)微流控装置,以测试检测Ab-pTK1免疫复合物作为临床血清样本中TK1分析第一步的可行性。我们能够使用含有0.01%吐温-20的0.5×磷酸盐缓冲盐水(PBS,pH 7.4)以及用作动态表面涂层和筛分基质的1%(w/v)甲基纤维素,从未结合的抗体中分离出免疫复合物。在5毫米的有效分离长度内观察到了抗体与Ab-pTK1复合物的分离。这种检测pTK1的方法易于操作,仅需10微升样品体积,分离仅需1分钟。

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