Resonance Raman Probes for Organelle-Specific Labeling in Live Cells

被引:42
|
作者
Kuzmin, Andrey N. [1 ]
Pliss, Artem [1 ]
Lim, Chang-Keun [1 ,2 ]
Heo, Jeongyun [1 ]
Kim, Sehoon [1 ,2 ]
Rzhevskii, Alexander [3 ]
Gu, Bobo [1 ,4 ]
Yong, Ken-Tye [5 ]
Wen, Shangchun [4 ]
Prasad, Paras N. [1 ]
机构
[1] Univ Buffalo, State Univ New York, Inst Lasers Photon & Biophoton, Buffalo, NY 14260 USA
[2] Korea Inst Sci & Technol, Ctr Theragnosis, Seoul 136791, South Korea
[3] Thermo Fisher Sci, Waltham, MA 02451 USA
[4] Hunan Univ, Sch Phys & Elect, Minist Educ, Key Lab Micro Nanooptoelect Devices, Changsha 410082, Hunan, Peoples R China
[5] Nanyang Technol Univ, Sch Elect & Elect Engn, Singapore 639798, Singapore
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
SPECTROSCOPY; SERS; DNA; TRANSFORMATIONS; MICROSCOPY;
D O I
10.1038/srep28483
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Raman microspectroscopy provides for high-resolution non-invasive molecular analysis of biological samples and has a breakthrough potential for dissection of cellular molecular composition at a single organelle level. However, the potential of Raman microspectroscopy can be fully realized only when novel types of molecular probes distinguishable in the Raman spectroscopy modality are developed for labeling of specific cellular domains to guide spectrochemical spatial imaging. Here we report on the design of a next generation Raman probe, based on BlackBerry Quencher 650 compound, which provides unprecedentedly high signal intensity through the Resonance Raman (RR) enhancement mechanism. Remarkably, RR enhancement occurs with low-toxic red light, which is close to maximum transparency in the biological optical window. The utility of proposed RR probes was validated for targeting lysosomes in live cultured cells, which enabled identification and subsequent monitoring of dynamic changes in this organelle by Raman imaging.
引用
收藏
页数:8
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