Enhanced weak-signal sensitivity in two-photon microscopy by adaptive illumination

被引:30
作者
Chu, Kengyeh K. [1 ]
Lim, Daryl [1 ]
Mertz, Jerome [1 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
关键词
D O I
10.1364/OL.32.002846
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We describe a technique to enhance both the weak-signal relative sensitivity and the dynamic range of a laser scanning optical microscope. The technique is based on maintaining a fixed detection power by fast feedback control of the illumination power, thereby transferring high measurement resolution to weak signals while virtually eliminating the possibility of image saturation. We analyze and demonstrate the benefits of adaptive illumination in two-photon fluorescence microscopy. (c) 2007 Optical Society of America.
引用
收藏
页码:2846 / 2848
页数:3
相关论文
共 5 条
[1]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[2]   Controlled light-exposure microscopy reduces photobleaching and phototoxicity in fluorescence live-cell imaging [J].
Hoebe, R. A. ;
Van Oven, C. H. ;
Gadella, T. W. J., Jr. ;
Dhonukshe, P. B. ;
Van Noorden, C. J. F. ;
Manders, E. M. M. .
NATURE BIOTECHNOLOGY, 2007, 25 (02) :249-253
[3]  
Meyer E., 2003, Scanning Probe Microscopy
[4]   Photobleaching in two-photon excitation microscopy [J].
Patterson, GH ;
Piston, DW .
BIOPHYSICAL JOURNAL, 2000, 78 (04) :2159-2162
[5]  
Pawley J.B., 2006, HDB BIOL CONFOCAL MI