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发夹探针点击聚合用于人 T 淋巴细胞病毒 II 型的无标记电化学检测

Hairpin probes based click polymerization for label-free electrochemical detection of human T-lymphotropic virus types II.

机构信息

Pharmacy College, Henan University of Chinese Medicine, Zhengzhou, 450008, PR China.

Pharmacy College, Henan University of Chinese Medicine, Zhengzhou, 450008, PR China.

出版信息

Anal Chim Acta. 2019 Jun 20;1059:86-93. doi: 10.1016/j.aca.2019.01.027. Epub 2019 Jan 25.

Abstract

A novel, simple, and label-free amplification electrochemical impedance method for quantitative detection of Human T-lymphotropic virus types II(HTLV-II) via click chemistry-mediated of hairpin DNA probes (hairpins) with polymers was developed. The hairpins were firstly attached to the gold electrode surface by an S-Au bond, the azido terminals of hairpins were close to the electrode surface, which make it difficult to be approached. After hybridizing with HTLV-II, the hairpins were unfolded and experienced a big configuration change, which made the azido terminals of the hairpins available to conjugate with alkynyl-containing polymer, called P(DEB-DSDA), formed by 1,4-diacetylenebenzene (DEB) and 4,4'-Diazido-2,2'-stilbenedisulfonic acid disodium salt tetrahydrate (DSDA) via Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC). With amount of P(DEB-DSDA) conjugated with the hairpin probes via click polymerization, its electrochemical signal can have a great amplification. Under optimized experimental conditions, this new probe showed a low detection limit of 0.171 pM with a good liner in the range of 1 pM-1 nM. Meanwhile, the biosensor also exhibited good selectivity and reliability in detection of real serum samples, indicating that it has great application potential in clinical DNA diagnosis and detection.

摘要

一种新颖、简单且无需标记的扩增电化学阻抗法,通过点击化学介导的发夹 DNA 探针(发夹)与聚合物,用于定量检测人类 T 淋巴细胞白血病病毒 II 型(HTLV-II)。发夹首先通过 S-Au 键附着在金电极表面,发夹的叠氮末端靠近电极表面,这使得它们难以接近。与 HTLV-II 杂交后,发夹展开并经历了很大的构象变化,使发夹的叠氮末端能够与炔基聚合物结合,该聚合物称为 P(DEB-DSDA),由 1,4-二乙炔基苯(DEB)和 4,4'-二叠氮基-2,2'-联苯二磺酸二钠盐四水合物(DSDA)通过 Cu(I)-催化的叠氮-炔环加成(CuAAC)形成。通过点击聚合与发夹探针结合的 P(DEB-DSDA)的数量,可以实现电化学信号的极大放大。在优化的实验条件下,该新探针的检测下限低至 0.171 pM,在 1 pM-1 nM 的范围内具有良好的线性关系。同时,该生物传感器在检测实际血清样本时也表现出良好的选择性和可靠性,表明其在临床 DNA 诊断和检测中具有很大的应用潜力。

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