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基于核酸适体的无标记电化学检测前列腺特异性抗原。

Label-free electrochemical detection of prostate-specific antigen based on nucleic acid aptamer.

机构信息

Univ. Paris Diderot, Sorbonne Paris Cité, ITODYS, UMR 7086 CNRS, 15 rue J-A de Baïf, 75205 Paris Cedex 13, France.

Univ. Paris Diderot, Sorbonne Paris Cité, ITODYS, UMR 7086 CNRS, 15 rue J-A de Baïf, 75205 Paris Cedex 13, France.

出版信息

Biosens Bioelectron. 2015 Jun 15;68:49-54. doi: 10.1016/j.bios.2014.12.033. Epub 2014 Dec 16.

DOI:10.1016/j.bios.2014.12.033
PMID:25569871
Abstract

We report a label-free aptasensor to make direct detection of prostate specific antigen (PSA, a biomarker of prostate cancer) using a quinone-containing conducting copolymer acting as redox transducer and grafting matrix for immobilization of the short aptamer strands. It is shown that capture of PSA generates a current decrease (signal-off) measured by Square Wave Voltammetry. This current decrease is specific for PSA above a limit of quantification in the ng mL(-1) range. The change in current is used to determine the PSA-aptamer dissociation constant K(D), of ca. 2.6 nM. To consolidate the proof of concept, a heterogeneous competitive exchange with a complementary DNA strand which breaks PSA-aptamer interactions is studied. This double-check followed by a current increase provides full assurance of a perfectly specific recognition.

摘要

我们报道了一种无标记适体传感器,使用含有醌的导电共聚物作为氧化还原转导体,并作为固定短适体链的接枝基质,直接检测前列腺特异性抗原 (PSA,前列腺癌的生物标志物)。结果表明,通过方波伏安法测量到 PSA 的捕获会产生电流下降(信号关闭)。这种电流下降是 PSA 在 ng mL(-1) 范围内定量限以上的特异性。电流的变化用于确定 PSA-适体解离常数 K(D),约为 2.6 nM。为了巩固概念验证,研究了与互补 DNA 链的非均相竞争交换,该链会破坏 PSA-适体相互作用。这种双检查后电流增加,完全保证了完全特异性识别。

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