Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy

被引:43
|
作者
Bowman, Adam J. [1 ]
Klopfer, Brannon B. [1 ]
Juffmann, Thomas [2 ,3 ]
Kasevich, Mark A. [1 ]
机构
[1] Stanford Univ, Phys Dept, 382 Via Pueblo Mall, Stanford, CA 94305 USA
[2] Univ Vienna, Fac Phys, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Struct & Computat Biol, Max F Perutz Labs, A-1030 Vienna, Austria
基金
美国国家科学基金会;
关键词
RESOLUTION; SPECTROSCOPY; PHOTOGRAPHY; ACQUISITION; FLIM; CELL;
D O I
10.1038/s41467-019-12535-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imaging. We demonstrate the use of Pockels cells for wide-field image gating with nanosecond temporal resolution and high photon collection efficiency. Two temporal frames are obtained by combining a Pockels cell with a pair of polarizing beam-splitters. We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-molecule lifetime spectroscopy, and fast single-frame FLIM at the camera frame rate with 10(3)-10(5) times higher throughput than single photon counting. Finally, we demonstrate a space-to-time image multiplexer using a re-imaging optical cavity with a tilted mirror to extend the Pockels cell technique to multiple temporal frames. These methods enable nanosecond imaging with standard optical systems and sensors, opening a new temporal dimension for wide-field low-light microscopy.
引用
收藏
页数:8
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