Literature DB >> 10233058

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

G Y Fan1, H Fujisaki, A Miyawaki, R K Tsay, R Y Tsien, M H Ellisman.   

Abstract

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 -3.1nu are also presented.

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Year:  1999        PMID: 10233058      PMCID: PMC1300213          DOI: 10.1016/S0006-3495(99)77396-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  15 in total

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  53 in total

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Review 9.  Technologies for imaging neural activity in large volumes.

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10.  Mechanism of the spatio-temporal regulation of Ras and Rap1.

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