Multifarious control of two-photon excitation of multiple fluorophores achieved by phase modulation of ultra-broadband laser pulses

被引:31
作者
Isobe, Keisuke [1 ]
Suda, Akira [1 ]
Tanaka, Masahiro [2 ]
Kannari, Fumihiko [2 ]
Kawano, Hiroyuki [3 ]
Mizuno, Hideaki [3 ]
Miyawaki, Atsushi [3 ]
Midorikawa, Katsumi [1 ]
机构
[1] RIKEN, Adv Sci Inst, Laser Technol Lab, Wako, Saitama 3510198, Japan
[2] Keio Univ, Dept Elect & Elect Engn, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
[3] RIKEN, Brain Sci Inst, Lab Cell Funct Dynam, Wako, Saitama 3510198, Japan
关键词
MULTIPHOTON INTRAPULSE INTERFERENCE; FLUORESCENCE MICROSCOPY; INDICATORS; PROTEINS; CA2+;
D O I
10.1364/OE.17.013737
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We propose two-photon excited fluorescence (TPEF) microscopy employing a novel phase modulation technique of ultra-broadband laser pulses, which allows the relative excitation of an individual fluorophore with respect to other fluorophores. This technique is based on the generation of multi-wavelength pulse train, which independently interacts with each fluorophore. Our technique is applied to dual-color imaging of cells expressing two types of fluorescent proteins. We achieve the selective excitation of one over the other and vice versa. The product of the maximum contrast ratios exceeds 100. We also demonstrate yielded equal excitation rates in the simultaneous excitation. By the selective excitation of a donor fluorescent protein, fluorescence resonance energy transfer imaging is also achieved. (C) 2009 Optical Society of America
引用
收藏
页码:13737 / 13746
页数:10
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