Department of Pharmaceutical Sciences, Nesbitt School of Pharmacy, Wilkes University, 84 W. South Street, Wilkes-Barre, PA 18766, USA.
Int J Mol Sci. 2020 Jul 18;21(14):5074. doi: 10.3390/ijms21145074.
Aptamers have gained an increasing role as the molecular recognition element (MRE) in diagnostic assay development, since their first conception thirty years ago. The process to screen for nucleic acid-based binding elements (aptamers) was first described in 1990 by the Gold Laboratory. In the last three decades, many aptamers have been identified for a wide array of targets. In particular, the number of reports on investigating single-stranded DNA (ssDNA) aptamer applications in biosensing and diagnostic platforms have increased significantly in recent years. This review article summarizes the recent (2015 to 2020) progress of ssDNA aptamer research on bacteria, proteins, and lipids of bacterial origins that have implications for human infections. The basic process of aptamer selection, the principles of aptamer-based biosensors, and future perspectives will also be discussed.
三十年前,适体作为分子识别元件(MRE)在诊断分析开发中发挥了越来越重要的作用。核酸结合元件(适体)的筛选过程于 1990 年由 Gold 实验室首次描述。在过去的三十年中,已经鉴定出了许多针对各种靶标的适体。特别是,近年来,关于研究单链 DNA(ssDNA)适体在生物传感和诊断平台中的应用的报告数量显著增加。本文综述了 2015 年至 2020 年期间 ssDNA 适体在与人类感染有关的细菌、蛋白质和细菌来源脂质研究方面的最新进展。还将讨论适体选择的基本过程、基于适体的生物传感器的原理和未来展望。