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基于适配体吸附磁性纳米颗粒的MPT64抗体比色法检测用于结核病诊断

Colorimetric Detection of MPT64 Antibody Based on an Aptamer Adsorbed Magnetic Nanoparticles for Diagnosis of Tuberculosis.

作者信息

Cheon Hong Jae, Lee Sang Min, Kim Seong-Rok, Shin Ho Yun, Seo Yiel Hea, Cho Yong Kyun, Lee Sang Pyo, Kim Moon Il

机构信息

Department of BioNano Technology, Gachon University, Seongnam, Gyeonggi 13120, Republic of Korea.

Division of Pulmonology and Allergy, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon 21565, Republic of Korea.

出版信息

J Nanosci Nanotechnol. 2019 Feb 1;19(2):622-626. doi: 10.1166/jnn.2019.15905.

Abstract

We have developed a colorimetric biosensing system for the detection of antibody against MPT64, a protein secreted by , using aptamer DNA adsorbed Fe₃O₄ magnetic nanoparticles (MNPs) for diagnosis of tuberculosis (TB). In this system, MNPs were first incubated with single stranded (ss) DNA-type aptamer having a high affinity toward target antibody against MPT64 (anti-MPT64), resulting in quick inhibition of the peroxidase-like activity of MNPs via the adsorption of aptamer on the surface of MNPs. By the addition of sample solutions containing anti-MPT64, aptamer bound on the surface of MNPs would strongly interact with free anti-MPT64 and be detached from the MNPs, thereby increasing the available surface area of the MNPs and consequently yielding enhanced peroxidase activity. Using this strategy, target anti-MPT64 was successfully detected by displaying increased colorimetric intensities from the higher oxidation of employed peroxidase substrate, 2,2'-azino-bis(3-ethylbenzo-thiazoline-6-sulfonic acid) (ABTS). Based on these results, we anticipate that aptamer adsorbed MNPs can serve as a potent probe system for the detection of clinically important target molecules.

摘要

我们开发了一种比色生物传感系统,用于检测针对MPT64的抗体。MPT64是由[具体细菌名称未给出]分泌的一种蛋白质,该系统利用吸附有适体DNA的Fe₃O₄磁性纳米颗粒(MNPs)来诊断结核病(TB)。在这个系统中,首先将MNPs与对针对MPT64的靶抗体(抗MPT64)具有高亲和力的单链(ss)DNA型适体一起孵育,由于适体吸附在MNPs表面,导致MNPs的过氧化物酶样活性迅速受到抑制。通过加入含有抗MPT64的样品溶液,结合在MNPs表面的适体将与游离的抗MPT64强烈相互作用并从MNPs上脱离,从而增加MNPs的可用表面积,进而产生增强的过氧化物酶活性。使用这种策略,通过显示所使用的过氧化物酶底物2,2'-联氮-双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)更高氧化程度下比色强度的增加,成功检测到了靶抗MPT64。基于这些结果,我们预计吸附有适体的MNPs可以作为检测临床重要靶分子的有效探针系统。

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