Department of Chemistry, The University of Texas at Austin, 105 East 24th Street A5300, Austin, Texas 78712-1224, USA.
Chem Soc Rev. 2021 Jan 7;50(1):9-38. doi: 10.1039/c9cs00538b. Epub 2020 Nov 10.
Indicator displacement assays (IDAs) offer a unique and innovative approach to molecular sensing. IDAs can facilitate the detection of a range of biologically/environmentally important species, provide a method for the detection of complex analytes or for the determination and discrimination of unknown sample mixtures. These attributes often cannot be achieved by traditional molecular sensors i.e. reaction-based sensors/chemosensors. The IDA pioneers Inouye, Shinkai, and Anslyn inspired researchers worldwide to develop various extensions of this idea. Since their early work, the field of indicator displacement assays has expanded to include: enantioselective indicator displacement assays (eIDAs), fluorescent indicator displacement assays (FIDAs), reaction-based indicator displacement assays (RIAs), DimerDye disassembly assays (DDAs), intramolecular indicator displacement assays (IIDAs), allosteric indicator displacement assay (AIDAs), mechanically controlled indicator displacement assays (MC-IDAs), and quencher displacement assays (QDAs). The simplicity of these IDAs, coupled with low cost, high sensitivity, and ability to carry out high-throughput automation analysis (i.e., sensing arrays) has led to their ubiquitous use in molecular sensing, alongside the other common approaches such as reaction-based sensors and chemosensors. In this review, we highlight the various design strategies that have been used to develop an IDA, including the design strategies for the newly reported extensions to these systems. To achieve this, we have divided this review into sections based on the target analyte, the importance of each analyte and then the reported IDA system is discussed. In addition, each section includes details on the benefit of the IDAs and perceived limitations for each system. We conclude this Tutorial Review by highlighting the current challenges associated with the development of new IDAs and suggest potential future avenues of research.
显色位移分析(IDA)为分子传感提供了一种独特而创新的方法。IDA 可以促进对一系列生物/环境重要物种的检测,为复杂分析物的检测或未知样品混合物的确定和区分提供一种方法。这些属性通常无法通过传统的分子传感器(即基于反应的传感器/化学传感器)来实现。IDA 的先驱者 Inouye、Shinkai 和 Anslyn 激励了全球研究人员开发了这一想法的各种扩展。自他们早期的工作以来,显色位移分析领域已经扩展到包括:对映选择性显色位移分析(eIDA)、荧光显色位移分析(FIDA)、基于反应的显色位移分析(RIA)、DimerDye 解体分析(DDA)、分子内显色位移分析(IIDA)、变构显色位移分析(AIDA)、机械控制显色位移分析(MC-IDA)和淬灭剂置换分析(QDA)。这些 IDA 的简单性,加上低成本、高灵敏度以及进行高通量自动化分析(即传感阵列)的能力,使得它们与基于反应的传感器和化学传感器等其他常见方法一起在分子传感中得到广泛应用。在这篇综述中,我们强调了已被用于开发 IDA 的各种设计策略,包括对这些系统新报告的扩展的设计策略。为了实现这一点,我们根据目标分析物将这篇综述分为几节,然后根据每个分析物的重要性讨论报告的 IDA 系统。此外,每个部分都包含有关 IDA 优势的详细信息以及每个系统的感知局限性。我们通过强调与新 IDA 开发相关的当前挑战并提出潜在的未来研究方向来结束本教程综述。