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Thrombin-linked aptamer assay for detection of platelet derived growth factor BB on magnetic beads in a sandwich format

机译:凝血酶连接的适体测定法以夹心形式检测磁珠上的血小板衍生生长因子BB

摘要

Here we describe a thrombin-linked aptamer assay (TLAA) for protein by using thrombin as an enzyme label, harnessing enzyme activity of thrombin and aptamer affinity binding. TLAA converts detection of specific target proteins to the detection of thrombin by using a DNA sequence that consists of two aptamers with the first aptamer binding to the specific target protein and the second aptamer binding to thrombin. Through the affinity binding, the thrombin enzyme is labeled on the protein target, and thrombin catalyzes the hydrolysis of small peptide substrate into product, generating signals for quantification. As a proof of principle, we show a sandwich TLAA for platelet derived growth factor BB (PDGF-BB) by using anti-PDGF-BB antibody coated on magnetic beads and an oligonucleotide containing the aptamer for PDGF-BB and the aptamer for thrombin. The binding of PDGF-BB to both the antibody and the aptamer results in labeling the complex with thrombin. We achieved detection of PDGF-BB at 16 pM. This TLAA contributes a new application of thrombin and its aptamer in bioanalysis, and shows potentials in assay developments. (C) 2016 Elsevier B.V. All rights reserved.
机译:在这里,我们通过使用凝血酶作为酶标记物,利用凝血酶的酶活性和适体亲和力结合来描述蛋白质的凝血酶连接适体测定法(TLAA)。 TLAA通过使用由两个适体组成的DNA序列将特异性靶蛋白的检测转换为凝血酶的检测,其中第一个适体与特异性靶蛋白结合,第二个适体与凝血酶结合。通过亲和力结合,凝血酶被标记在蛋白质靶标上,凝血酶催化小肽底物水解成产物,产生定量信号。作为原理的证明,我们通过使用包被在磁珠上的抗PDGF-BB抗体和含有PDGF-BB适体和凝血酶适体的寡核苷酸,显示了血小板衍生生长因子BB(PDGF-BB)的三明治TLAA。 PDGF-BB与抗体和适体两者的结合导致用凝血酶标记复合物。我们在16 pM时检测到PDGF-BB。该TLAA促进了凝血酶及其适体在生物分析中的新应用,并显示了测定开发的潜力。 (C)2016 Elsevier B.V.保留所有权利。

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    Guo Limin; Zhao Qiang;

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  • 年度 2016
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