Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.
Chem Soc Rev. 2013 Apr 21;42(8):3427-40. doi: 10.1039/c2cs35472a.
Breakthrough advances in chemistry and biology over the last two decades have vastly expanded the repertoire of nucleic acid structure and function with potential application in multiple areas of science and technology, including sensing and analytical applications. DNA oligonucleotides represent popular tools for the development of sensing platforms due to their low cost, rich structural polymorphism, and their ability to bind to cognate ligands with sensitivity and specificity rivaling those for protein enzymes and antibodies. In this review, we give an overview of the "label-free" approach that has been a particular focus of our group and others for the construction of luminescent DNA-based sensing platforms. The label-free strategy aims to overcome some of the drawbacks associated with the use of covalently-labeled oligonucleotides prevalent in electrochemical and optical platforms. Label-free DNA-based probes harness the selective interaction between luminescent dyes and functional oligonucleotides that exhibit a "structure-switching" response upon binding to analytes. Based on the numerous examples of label-free luminescent DNA-based probes reported recently, we envisage that this field would continue to thrive and mature in the years to come.
过去二十年中,化学和生物学的突破性进展极大地扩展了核酸结构和功能的范围,在包括传感和分析应用在内的多个科学和技术领域具有潜在的应用。由于其低成本、丰富的结构多态性以及与同源配体结合的敏感性和特异性可与蛋白质酶和抗体相媲美,因此 DNA 寡核苷酸是开发传感平台的常用工具。在这篇综述中,我们概述了“无标记”方法,这是我们小组和其他小组特别关注的一个方法,用于构建基于 DNA 的发光传感平台。无标记策略旨在克服与电化学和光学平台中普遍使用的共价标记寡核苷酸相关的一些缺点。无标记的 DNA 探针利用发光染料与功能性寡核苷酸之间的选择性相互作用,这些寡核苷酸在与分析物结合时表现出“结构转变”反应。根据最近报道的众多无标记发光 DNA 探针的例子,我们预计该领域在未来几年将继续蓬勃发展并成熟。