Two-color two-photon 4Pi fluorescence microscopy

被引:20
作者
Chen, JF
Midorikawa, K
机构
[1] RIKEN, Laser Technol Lab, Wako, Saitama 3510198, Japan
[2] Saitama Univ, Saitama City, Saitama 3388570, Japan
关键词
D O I
10.1364/OL.29.001354
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
In 4Pi fluorescence microscopy the point-spread function is composed of a strong central lobe accompanied by interference sidelobes that produce artifacts in the image. We propose to combine two-color two-photon fluorescence microscopy and 4Pi fluorescence microscopy to overcome this sidelobe problem. Simulation results show that a single sharp fluorescence spot can be produced by use of two excitation wavelengths of 400 and 800 nm and detected at 350-nm emission wavelength. (C) 2004 Optical Society of America.
引用
收藏
页码:1354 / 1356
页数:3
相关论文
共 12 条
[1]   Advantages of two-color excitation fluorescence microscopy with two confocal excitation beams [J].
Cambaliza, MO ;
Saloma, C .
OPTICS COMMUNICATIONS, 2000, 184 (1-4) :25-35
[2]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[3]   Focal spots of size λ/23 open up far-field florescence microscopy at 33 nm axial resolution -: art. no. 163901 [J].
Dyba, M ;
Hell, SW .
PHYSICAL REVIEW LETTERS, 2002, 88 (16) :4-163901
[4]   Focusing of light through a stratified medium:: a practical approach for computing microscope point spread functions.: Part I:: Conventional microscopy [J].
Haeberlé, O .
OPTICS COMMUNICATIONS, 2003, 216 (1-3) :55-63
[5]   PROPERTIES OF A 4PI CONFOCAL FLUORESCENCE MICROSCOPE [J].
HELL, S ;
STELZER, EHK .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1992, 9 (12) :2159-2166
[6]   FUNDAMENTAL IMPROVEMENT OF RESOLUTION WITH A 4PI-CONFOCAL FLUORESCENCE MICROSCOPE USING 2-PHOTON EXCITATION [J].
HELL, S ;
STELZER, EHK .
OPTICS COMMUNICATIONS, 1992, 93 (5-6) :277-282
[7]  
LACOWICZ JR, 1996, PHOTOCHEM PHOTOBIOL, V64, P632
[8]  
LACOWICZ JR, 1996, J PHYS CHEM-US, V100, P19406
[9]   MEMOIR ON INVENTING THE CONFOCAL SCANNING MICROSCOPE [J].
MINSKY, M .
SCANNING, 1988, 10 (04) :128-138
[10]   Coherent use of opposing lenses for axial resolution increase in fluorescence microscopy. I. Comparative study of concepts [J].
Nagorni, M ;
Hell, SW .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 2001, 18 (01) :36-48