Transient absorption imaging of hemes with 2-color, independently tunable visible-wavelength ultrafast source

被引:17
|
作者
Domingue, Scott R. [1 ,4 ]
Bartels, Randy A. [1 ,3 ]
Chicco, Adam J. [2 ,3 ]
Wilson, Jesse W. [1 ,3 ]
机构
[1] Colorado State Univ, Dept Elect & Comp Engn, Ft Collins, CO 80523 USA
[2] Colorado State Univ, Dept Biomed Sci, Ft Collins, CO 80523 USA
[3] Colorado State Univ, Sch Biomed Engn, Ft Collins, CO 80523 USA
[4] KMLabs, Boulder, CO USA
来源
BIOMEDICAL OPTICS EXPRESS | 2017年 / 8卷 / 06期
关键词
ALL-NORMAL-DISPERSION; SUPERCONTINUUM GENERATION; WAVE-BREAKING; IN-VIVO; FLUORESCENCE; MICROSCOPY; SPECTROSCOPY; PULSES; CHROMOPHORES; COMPRESSION;
D O I
10.1364/BOE.8.002807
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pump probe microscopy is a time-resolved multiphoton imaging technique capable of generating contrast between non-fluorescent pigments based on differences in excited-state lifetimes. Here we describe a fiber-based ultrafast system designed for imaging heme proteins with an independently-tunable pulse pair in the visible-wavelength regime. Starting with a 1060 nm fiber amplifier (1.3Wat 63MHz, 140 fs pulses), visible pulses were produced in the vicinity of 488 nm and 532 nm by doubling the output of a short photonic crystal fiber with a pair of periodically-poled lithium niobate crystals, providing 5-20 mW power in each beam. This was sufficient for acquiring transient absorption images from unstained cryosectioned tissue. (C) 2017 Optical Society of America
引用
收藏
页码:2807 / 2821
页数:15
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