Department of Chemistry, Columbia University, New York, NY 10027, United States of America.
Phys Biol. 2019 Apr 23;16(4):041003. doi: 10.1088/1478-3975/ab0fcd.
Optical microscopy has served biomedical research for decades due to its high temporal and spatial resolutions. Among various optical imaging techniques, fluorescence imaging offers superb sensitivity down to single molecule level but its multiplexing capacity is limited by intrinsically broad bandwidth. To simultaneously capture a vast number of targets, the newly emerging vibrational microscopy technique draws increasing attention as vibration spectroscopy features narrow transition linewidth. Nonetheless, unlike fluorophores that have been studied for centuries, a systematic investigation on vibrational probes is underemphasized. Herein, we reviewed some of the recent developments of vibrational probes for multiplex imaging applications, particularly those serving stimulated Raman scattering (SRS) microscopy, which is one of the most promising vibrational imaging techniques. We wish to summarize the general guidelines for developing bioorthogonal vibrational probes with high sensitivity, chemical specificity and most importantly, tunability to fulfill super-multiplexed optical imaging. Future directions to significantly improve the performance are also discussed.
光学显微镜由于具有高时空分辨率,在生物医学研究中已经使用了几十年。在各种光学成像技术中,荧光成像是最灵敏的,可达到单分子水平,但由于固有带宽较宽,其多重成像是有限的。为了同时捕获大量目标,新出现的振动显微镜技术受到越来越多的关注,因为振动光谱具有较窄的跃迁线宽。然而,与已经研究了几个世纪的荧光团不同,对振动探针的系统研究被低估了。在此,我们综述了用于多重成像应用的振动探针的一些最新进展,特别是用于受激拉曼散射(SRS)显微镜的那些进展,SRS 显微镜是最有前途的振动成像技术之一。我们希望总结出开发具有高灵敏度、化学特异性且最重要的是可调谐性的生物正交振动探针的一般原则,以实现超多重光学成像。还讨论了提高性能的未来方向。