Raman spectroscopy and microscopy of individual cells and cellular components

被引:116
作者
Chan, James [1 ,2 ]
Fore, Samantha [1 ]
Wachsman-Hogiu, Sebastian [1 ]
Huser, Thomas [1 ,3 ]
机构
[1] Univ Calif Davis, NSF Ctr Biophoton Sci & Technol, Sacramento, CA 95817 USA
[2] Lawrence Livermore Natl Lab, Phys Sci Directorate, Livermore, CA 94550 USA
[3] Univ Calif Davis, Dept Internal Med, Sacramento, CA 95817 USA
关键词
Raman spectroscopy; laser tweezers; coherent anti-Stokes Raman scattering; CARS microscopy; surface-enhanced Raman spectroscopy; SERS; nanoparticles; time-correlated single-photon counting; single-cell microscopy;
D O I
10.1002/lpor.200810012
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Raman spectroscopy provides the unique opportunity to nondestructively analyze chemical concentrations in individual cells on the submicrometer length scale without the need for optical labels. This enables the rapid assessment of cellular biochemistry inside living cells, and it allows for their continued analysis. Here, we review recent developments in the analysis of single cells, subcellular compartments, and chemical imaging based on Raman spectroscopy. Spontaneous Raman spectroscopy provides for the full spectral assessment of cellular biochemistry, while coherent Raman techniques, such as coherent anti-Stokes Raman scattering is primarily used as an imaging tool comparable to confocal fluorescence microscopy. These techniques are complemented by surface-enhanced Raman spectroscopy, which provides higher sensitivity and local specificity, and also extends the techniques to chemical indicators, i.e. pH sensing. We review the strengths and weaknesses of each technique, demonstrate some of their applications and discuss their potential for future research in cell biology and biomedicine.
引用
收藏
页码:325 / 349
页数:25
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