Resonant Electro-Optic Imaging for Microscopy at Nanosecond Resolution

被引:11
|
作者
Bowman, Adam J. [1 ]
Kasevich, Mark A. [1 ]
机构
[1] Stanford Univ, Phys Dept, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
FLIM; single-molecule; super-resolution; nanosecond imaging; electro-optic; Pockels cell; wide-field; RESOLVED FLUORESCENCE ANISOTROPY; SINGLE-MOLECULE SPECTROSCOPY; PHOTON ECONOMY; IN-VIVO; LIFETIME; ACQUISITION; SENSITIVITY; DYNAMICS; FRET; EXCITATION;
D O I
10.1021/acsnano.1c04470
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate an electro-optic wide-field method to enable fluorescence lifetime microscopy (FLIM) with high throughput and single-molecule sensitivity. Resonantly driven Pockels cells are used to efficiently gate images at 39 MHz, allowing fluorescence lifetime to be captured on standard camera sensors. Lifetime imaging of single molecules is enabled in wide field with exposure times of less than 100 ms. This capability allows combination of wide-field FLIM with single-molecule super-resolution localization microscopy. Fast single-molecule dynamics such as FRET and molecular binding events are captured from wide-field images without prior spatial knowledge. A lifetime sensitivity of 1.9 times the photon shot-noise limit is achieved, and high throughput is shown by acquiring wide-field FLIM images with millisecond exposure and >10(8) photons per frame. Resonant electro-optic FLIM allows lifetime contrast in any wide-field microscopy method.
引用
收藏
页码:16043 / 16054
页数:12
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