期刊
BIOMEDICAL OPTICS EXPRESS
卷 2, 期 4, 页码 927-936出版社
OPTICAL SOC AMER
DOI: 10.1364/BOE.2.000927
关键词
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资金
- Japan Science and Technology (JST) organization via a CREST
- RIKEN
- Grants-in-Aid for Scientific Research [21226003] Funding Source: KAKEN
We employed deep UV (DUV) Raman spectroscopy for characterization of molecular photodamage in cells. 244 nm light excitation Raman spectra were measured for HeLa cells exposed to the excitation light for different durations. In the spectra obtained with the shortest exposure duration (0.25 sec at 16 mu W/mu m(2) irradiation), characteristic resonant Raman bands of adenine and guanine at 1483 cm(-1) and tryptophan and tyrosine at 1618 cm(-1) were clearly visible. With increasing exposure duration (up to 12.5 sec), these biomolecular Raman bands diminished, while a photoproduct Raman band at 1611 cm(-1) grew. By exponential function fitting analyses, intensities of these characteristic three bands were correlated with sample exposure duration at different intensities of excitation light. We then suggest practical excitation conditions effective for DUV Raman observation of cells without photodamage-related spectral distortion. (C) 2011 Optical Society of America
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