Haisch Christoph
Technische Universität München, Marchioninistrasse 17, 81377, Munich, Germany.
Anal Bioanal Chem. 2016 Jul;408(17):4535-45. doi: 10.1007/s00216-016-9444-9. Epub 2016 Mar 14.
For a quarter of a century, microarrays have been part of the routine analytical toolbox. Label-based fluorescence detection is still the commonest optical readout strategy. Since the 1990s, a continuously increasing number of label-based as well as label-free experiments on Raman-based microarray readout concepts have been reported. This review summarizes the possible concepts and methods and their advantages and challenges. A common label-based strategy is based on the binding of selective receptors as well as Raman reporter molecules to plasmonic nanoparticles in a sandwich immunoassay, which results in surface-enhanced Raman scattering signals of the reporter molecule. Alternatively, capture of the analytes can be performed by receptors on a microarray surface. Addition of plasmonic nanoparticles again leads to a surface-enhanced Raman scattering signal, not of a label but directly of the analyte. This approach is mostly proposed for bacteria and cell detection. However, although many promising readout strategies have been discussed in numerous publications, rarely have any of them made the step from proof of concept to a practical application, let alone routine use. Graphical Abstract Possible realization of a SERS (Surface-Enhanced Raman Scattering) system for microarray readout.
在四分之一个世纪里,微阵列一直是常规分析工具箱的一部分。基于标记的荧光检测仍然是最常见的光学读出策略。自20世纪90年代以来,基于拉曼的微阵列读出概念的基于标记以及无标记的实验报道数量一直在不断增加。本综述总结了可能的概念和方法及其优点和挑战。一种常见的基于标记的策略是在夹心免疫分析中,选择性受体以及拉曼报告分子与等离子体纳米颗粒结合,这会导致报告分子的表面增强拉曼散射信号。或者,可以通过微阵列表面的受体捕获分析物。再次添加等离子体纳米颗粒会导致表面增强拉曼散射信号,不是标记的信号,而是直接来自分析物的信号。这种方法主要用于细菌和细胞检测。然而,尽管众多出版物中讨论了许多有前景的读出策略,但它们很少有从概念验证迈向实际应用的,更不用说常规使用了。图形摘要微阵列读出的表面增强拉曼散射(SERS)系统的可能实现方式。