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抗结核分枝杆菌 Ag85A 的 DNA 适体的筛选及其在基于氧化石墨烯的荧光测定法中的应用。

Selection of DNA aptamers against Mycobacterium tuberculosis Ag85A, and its application in a graphene oxide-based fluorometric assay.

机构信息

Department of Microbiology and Virology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, 91778-99191, Iran.

Antimicrobial Resistance Research Center, Buali Research Institute, Department of Microbiology and Virology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, 91778-99191, Iran.

出版信息

Mikrochim Acta. 2017 Dec 5;185(1):21. doi: 10.1007/s00604-017-2550-3.

Abstract

The Mycobacterium Ag85 complex is the major secretory protein of M. tuberculosis. It is a potential marker for early diagnosis of tuberculosis (TB). The authors have identified specific aptamers for Ag85A (FbpA) via protein SELEX using magnetic beads. After twelve rounds of selection, two aptamers (Apt8 and Apt22) were chosen from different groups, and their binding constants were determined by flow cytometry. Apt22 (labeled with Atto 647N) binds to FbpA with high affinity (K = 63 nM) and specificity. A rapid, sensitive, and low-cost fluorescent assay was designed based on the use of Apt22 and graphene oxide, with a limit of detection of 1.5 nM and an analytical range from 5 to 200 nM of FbpA. Graphical abstract Schematic illustration of graphene oxide-based aptasensor for fluorometric determination of FbpA.

摘要

结核分枝杆菌 Ag85 复合物是结核分枝杆菌主要的分泌性蛋白,它是一种用于早期诊断结核病(TB)的潜在标志物。作者通过使用磁性珠的蛋白质 SELEX 方法鉴定了 Ag85A(FbpA)的特异性适体。经过十二轮筛选,从不同的组中选择了两个适体(Apt8 和 Apt22),并通过流式细胞术确定了它们的结合常数。Apt22(用 Atto 647N 标记)与 FbpA 具有高亲和力(K=63 nM)和特异性结合。基于 Apt22 和氧化石墨烯的使用,设计了一种快速、灵敏且低成本的荧光测定法,其检测限为 1.5 nM,分析范围为 5 至 200 nM 的 FbpA。

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