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用于活细胞动态分子成像的拉曼显微镜。

Raman microscopy for dynamic molecular imaging of living cells.

作者信息

Hamada Keisaku, Fujita Katsumasa, Smith Nicholas Isaac, Kobayashi Minoru, Inouye Yasushi, Kawata Satoshi

机构信息

Osaka University, Department of Frontier Biosciences, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

J Biomed Opt. 2008 Jul-Aug;13(4):044027. doi: 10.1117/1.2952192.

Abstract

We demonstrate dynamic imaging of molecular distribution in unstained living cells using Raman scattering. By combining slit-scanning detection and optimizing the excitation wavelength, we imaged the dynamic molecular distributions of cytochrome c, protein beta sheets, and lipids in unstained HeLa cells with a temporal resolution of 3 minutes. We found that 532-nm excitation can be used to generate strong Raman scattering signals and to suppress autofluorescence that typically obscures Raman signals. With this technique, we reveal time-resolved distributions of cytochrome c and other biomolecules in living cells in the process of cytokinesis without the need for fluorescent labels or markers.

摘要

我们展示了利用拉曼散射对未染色活细胞中的分子分布进行动态成像。通过结合狭缝扫描检测并优化激发波长,我们以3分钟的时间分辨率对未染色的HeLa细胞中细胞色素c、蛋白质β折叠和脂质的动态分子分布进行了成像。我们发现532纳米激发可用于产生强烈的拉曼散射信号,并抑制通常会掩盖拉曼信号的自发荧光。通过这项技术,我们揭示了在细胞分裂过程中活细胞中细胞色素c和其他生物分子的时间分辨分布,而无需荧光标记或标志物。

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