Single-laser-based simultaneous four-wavelength excitation source for femtosecond two-photon fluorescence microscopy

被引:6
|
作者
Hsiao, Yang-Ting [1 ]
Huang, Yu-Fan [2 ]
Borah, Bhaskar Jyoti [1 ]
Chen, Shih-Kuo [2 ]
Sun, Chi-Kuang [1 ]
机构
[1] Natl Taiwan Univ, Dept Elect Engn, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Dept Life Sci, Taipei 10617, Taiwan
来源
BIOMEDICAL OPTICS EXPRESS | 2021年 / 12卷 / 08期
关键词
SELF-PHASE-MODULATION; CHERENKOV RADIATION; HIGHLY EFFICIENT; VISIBLE WAVELENGTH; NEURONAL-ACTIVITY; DISPERSIVE WAVE; GENERATION; PROTEINS; PLATFORM; SOLITONS;
D O I
10.1364/BOE.428771
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multicolor labeling of biological samples with large volume is required for omic-level of study such as the construction of nervous system connectome. Among the various imaging method, two photon microscope has multiple advantages over traditional single photon microscope for higher resolution and could image large 3D volumes of tissue samples with superior imaging depth. However, the growing number of fluorophores for labeling underlines the urgent need for an ultrafast laser source with the capability of providing simultaneous plural excitation wavelengths for multiple fluorophores. Here, we propose and demonstrate a single-laser-based four-wavelength excitation source for two-photon fluorescence microscopy. Using a sub-100 fs 1,070-nm Yb:fiber laser to pump an ultrashort nonlinear photonic crystal fiber in the low negative dispersion region, we introduced efficient self-phase modulation and acquired a blue-shifted spectrum dual-peaked at 812 and 960 nm with 28.5% wavelength conversion efficiency. By compressing the blue-shift near-IR spectrum to 33 fs to ensure the temporal overlap of the 812 and 960 nm peaks, the so-called sum frequency effect created the third virtual excitation wavelength effectively at 886 nm. Combined with the 1,070 nm laser source as the fourth excitation wavelength, the all-fiber-format four-wavelength excitation source enabled simultaneous four-color two-photon imaging in Brainbow AAV-labeled (TagBFP, mTFP, EYFP, and mCherry) brain samples. With an increased number of excitation wavelengths and improved excitation efficiency than typical commercial femtosecond lasers, our compact four-wavelength excitation approach can provide a versatile, efficient, and easily accessible solution for multiple-color two-photon fluorescence imaging in the field of neuroscience, biomolecular probing, and clinical applications with at least four spectrally-distinct fluorophores. (c) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:4661 / 4679
页数:19
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