Masked illumination scheme for a galvanometer scanning high-speed confocal fluorescence microscope.

High-speed beam scanning and data acquisition in a laser scanning confocal microscope system are normally implemented with a resonant galvanometer scanner and a frame grabber. However, the nonlinear scanning speed of a resonant galvanometer can generate nonuniform photobleaching in a fluorescence sample as well as image distortion near the edges of a galvanometer scanned fluorescence image. Besides, incompatibility of signal format between a frame grabber and a point detector can lead to digitization error during data acquisition. In this article, we introduce a masked illumination scheme which can effectively decrease drawbacks in fluorescence images taken by a laser scanning confocal microscope with a resonant galvanometer and a frame grabber. We have demonstrated that the difference of photobleaching between the center and the edge of a fluorescence image can be reduced from 26 to 5% in our confocal laser scanning microscope with a square illumination mask. Another advantage of our masked illumination scheme is that the zero level or the lowest input level of an analog signal in a frame grabber can be accurately set by the dark area of a mask in our masked illumination scheme. We have experimentally demonstrated the advantages of our masked illumination method in detail.

[1]  R. Vandenbroucke,et al.  Line FRAP with the confocal laser scanning microscope for diffusion measurements in small regions of 3-D samples. , 2007, Biophysical journal.

[2]  L Leybaert,et al.  A simple and practical method to acquire geometrically correct images with resonant scanning‐based line scanning in a custom‐built video‐rate laser scanning microscope , 2005, Journal of microscopy.

[3]  Takeo Tanaami,et al.  High-speed 1-frame/ms scanning confocal microscope with a microlens and Nipkow disks. , 2002, Applied optics.

[4]  W B Amos,et al.  How the Confocal Laser Scanning Microscope entered Biological Research , 2003, Biology of the cell.

[5]  Brian J. Bacskai,et al.  Video-Rate Confocal Microscopy , 1995 .

[6]  I. Parker,et al.  Construction of a confocal microscope for real-time x-y and x-z imaging. , 1999, Cell calcium.

[7]  E. Stelzer The Intermediate Optical System of Laser-Scanning Confocal Microscopes , 2006 .

[8]  Herbert Zettl Video Basics , 1997 .

[9]  C W Balke,et al.  A custom confocal and two-photon digital laser scanning microscope. , 2000, American journal of physiology. Heart and circulatory physiology.

[10]  R A Robb,et al.  Three-dimensional reconstruction of aqueous channels in human trabecular meshwork using light microscopy and confocal microscopy. , 2006, Scanning.

[11]  Francesca Cella,et al.  A New FRAP/FRAPa Method for Three-Dimensional Diffusion Measurements Based on Multiphoton Excitation Microscopy , 2008, Biophysical journal.

[12]  W. Wier,et al.  A high-resolution, confocal laser-scanning microscope and flash photolysis system for physiological studies. , 1997, Cell calcium.

[13]  I. Esteve,et al.  The biomass dynamics of cyanobacteria in an annual cycle determined by confocal laser scanning microscopy. , 2006, Scanning.