HIV-1 Tat peptide detection by using RNA aptamer on MWCNT modified electrode

M. S. Radhi, A. R. Ruslinda, M. F. Fatin, S. S. B. Hashwan, M. Arshad, U. Hashim
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引用次数: 2

Abstract

An electrode has been fabricated for detection of HIV-1 Tat protein. Functionalized carboxylated multiwalled carbon nanotube (COOH-MWCNT) has been deposited by spray technique on the electrode to act as amplification layer and immobilization site for aptamer. Aptamer has been proved that it is highly specific for the detection of its target molecule. In this paper, we demonstrated the immobilization of split aptamer on MWCNT-modified electrode by interaction of carboxyl functional group from MWCNT and amine functional group from aptamer. The implementation of split RNA aptamer as a recognition element is promising for detecting HIV-1 Tat peptide. Detection has been conducted in control sample and HIV-1 Tat protein sample. The intercalation of aptamer and protein has given changes to the electrical signal and quantified by picoammeter showing decrease in current value of 3.74nA compared to control which different only 1.64nA.
MWCNT修饰电极上RNA适体检测HIV-1 Tat肽
制备了一种检测HIV-1 Tat蛋白的电极。采用喷雾法制备羧基化功能化多壁碳纳米管(COOH-MWCNT)作为适配体的扩增层和固定位点。适体已被证明对其靶分子的检测具有高度的特异性。本文利用纳米碳纳米管的羧基官能团和胺基官能团的相互作用,证明了分裂适体在纳米碳纳米管修饰电极上的固定化。分裂RNA适体作为识别元件的实现有望用于检测HIV-1 Tat肽。对对照样品和HIV-1 Tat蛋白样品进行了检测。适配体和蛋白质的插入使电信号发生变化,并通过皮安计进行了量化,结果显示电流值比对照组减少了3.74nA,仅相差1.64nA。
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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