Convergence of Surface-Enhanced Raman Scattering with Molecular Diagnostics: A Perspective on Future Directions

被引:16
|
作者
Choi, Namhyun [1 ,2 ,3 ]
Schluecker, Sebastian [1 ,2 ,3 ]
机构
[1] Univ Duisburg Essen UDE, Dept Chem, Phys Chem 1, D-45141 Essen, Germany
[2] Univ Duisburg Essen UDE, Ctr Nanointegrat Duisburg Essen CENIDE, D-45141 Essen, Germany
[3] Univ Duisburg Essen UDE, Ctr Med Biotechnol ZMB, D-45141 Essen, Germany
基金
新加坡国家研究基金会;
关键词
Surface-enhanced Ramanscattering; SERS; Moleculardiagnostics; PCR; CRISPR/Cas; SHERLOCK; DETECTR; NUCLEIC-ACID DETECTION; ENZYMATIC AMPLIFICATION; DEOXYRIBONUCLEIC-ACID; MULTIPLEX DETECTION; PRENATAL-DIAGNOSIS; DNA; SPECTROSCOPY; PCR; ASSAY; MUTATIONS;
D O I
10.1021/acsnano.3c11370
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular diagnostics (MD) is widely employed in multiple scientific disciplines, such as oncology, pathogen detection, forensic investigations, and the pharmaceutical industry. Techniques such as polymerase chain reaction (PCR) revolutionized the rapid and accurate identification of nucleic acids (DNA, RNA). More recently, CRISPR and its CRISPR-associated protein (Cas) have been a ground-breaking discovery that is the latest revolution in molecular biology, including MD. Surface-enhanced Raman scattering (SERS) is a very attractive alternative to fluorescence as the currently most widely used optical readout in MD. In this Perspective, milestones in the development of MD, SERS-PCR, and next-generation approaches to MD, such as Specific High-Sensitivity Enzymatic Reporter UnLOCKing (SHERLOCK) and DNA Endonuclease-Targeted CRISPR Trans Reporter (DETECTR), are briefly summarized. Our perspective on the future convergence of SERS with MD is focused on SERS-based CRISPR/Cas (SERS-CRISPR) since we anticipate many promising applications in this rapidly emerging field. We predict that major future developments will exploit the advantages of real-time monitoring with the superior brightness, photostability, and spectral multiplexing potential of SERS nanotags in an automated workflow for rapid assays under isothermal, amplification-free conditions.
引用
收藏
页码:5998 / 6007
页数:10
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