Video-rate scanning two-photon excitation fluorescence microscopy and ratio imaging with cameleons

被引:186
作者
Fan, GY [1 ]
Fujisaki, H
Miyawaki, A
Tsay, RK
Tsien, RY
Ellisman, MH
机构
[1] Univ Calif San Diego, Natl Ctr Microscopy & Imaging Res, Dept Neurosci, Sch Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[4] Nikon Inc, Tsukuba Res Labs, Ibaraki, Osaka 3002635, Japan
关键词
D O I
10.1016/S0006-3495(99)77396-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A video-rate (30 frames/s) scanning two-photon excitation microscope has been successfully tested. The microscope, based on a Nikon RCM 8000, incorporates a femtosecond pulsed laser with wavelength tunable from 690 to 1050 nm, prechirper optics for laser pulse-width compression, resonant galvanometer for video-rate point scanning, and a pair of nonconfocal detectors for fast emission ratioing. An increase in fluorescent emission of 1.75-fold is consistently obtained with the use of the prechirper optics. The nonconfocal detectors provide another 2.25-fold increase in detection efficiency. Ratio imaging and optical sectioning can therefore be performed more efficiently without confocal optics. Faster frame rates, at 60, 120, and 240 frames/s, can be achieved with proportionally reduced scan lines per frame. Useful two-photon images can be acquired at video rate with a laser power as low as 2.7 mW at specimen with the genetically modified green fluorescent proteins. Preliminary results obtained using this system confirm that the yellow "cameleons" exhibit similar optical properties as under one-photon excitation conditions. Dynamic two-photon images of cardiac myocytes and ratio images of yellow cameleon-2.1, -3.1, and -3.lnu are also presented.
引用
收藏
页码:2412 / 2420
页数:9
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