Highly specific label-free molecular imaging with spectrally tailored excitation-stimulated Raman scattering (STE-SRS) microscopy

被引:131
作者
Freudiger, Christian W. [1 ,2 ]
Min, Wei [1 ]
Holtom, Gary R. [1 ]
Xu, Bingwei [3 ]
Dantus, Marcos [4 ,5 ]
Xie, X. Sunney [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[3] Biophoton Solut Inc, E Lansing, MI 48823 USA
[4] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[5] Michigan State Univ, Dept Phys, E Lansing, MI 48824 USA
基金
美国国家卫生研究院;
关键词
CARS SPECTROSCOPY; IN-VIVO; COHERENT; FLUORESCENCE; SENSITIVITY; PHOTODAMAGE; TISSUE; PHASE;
D O I
10.1038/NPHOTON.2010.294
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Label-free microscopy that has chemical contrast and high acquisition speeds up to video rates has recently been made possible using stimulated Raman scattering (SRS) microscopy. SRS imaging offers high sensitivity, but the spectral specificity of the original narrowband implementation is limited, making it difficult to distinguish chemical species with overlapping Raman bands. Here, we present a highly specific imaging method that allows mapping of a particular chemical species in the presence of interfering species, based on tailored multiplex excitation of its vibrational spectrum. This is implemented by spectral modulation of a broadband pump beam at a high frequency (>1 MHz), allowing detection of the SRS signal of the narrowband Stokes beam with high sensitivity. Using the scheme, we demonstrate quantification of cholesterol in the presence of lipids, and real-time three-dimensional spectral imaging of protein, stearic acid and oleic acid in live Caenorhabditis elegans.
引用
收藏
页码:103 / 109
页数:7
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