Digitally synthesized beat frequency-multiplexed fluorescence lifetime spectroscopy

被引:9
作者
Chan, Jacky C. K. [1 ]
Diebold, Eric D. [1 ,2 ]
Buckley, Brandon W. [1 ]
Mao, Sien [1 ]
Akbari, Najva [1 ]
Jalali, Bahram [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Elect Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2014年 / 5卷 / 12期
关键词
IMAGING MICROSCOPY FLIM; TIME; RESOLUTION; SPEED; DECAY; ACQUISITION; EXCITATION; STANDARDS; SYSTEM; PHASE;
D O I
10.1364/BOE.5.004428
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Frequency domain fluorescence lifetime imaging is a powerful technique that enables the observation of subtle changes in the molecular environment of a fluorescent probe. This technique works by measuring the phase delay between the optical emission and excitation of fluorophores as a function of modulation frequency. However, high-resolution measurements are time consuming, as the excitation modulation frequency must be swept, and faster low-resolution measurements at a single frequency are prone to large errors. Here, we present a low cost optical system for applications in real-time confocal lifetime imaging, which measures the phase vs. frequency spectrum without sweeping. Deemed Lifetime Imaging using Frequency-multiplexed Excitation (LIFE), this technique uses a digitally-synthesized radio frequency comb to drive an acousto-optic deflector, operated in a cat's-eye configuration, to produce a single laser excitation beam modulated at multiple beat frequencies. We demonstrate simultaneous fluorescence lifetime measurements at 10 frequencies over a bandwidth of 48 MHz, enabling high speed frequency domain lifetime analysis of single-and multi-component sample mixtures. (C) 2014 Optical Society of America
引用
收藏
页码:4428 / 4436
页数:9
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