A custom confocal and two-photon digital laser scanning microscope

被引:23
作者
Wier, WG
Balke, CW
Michael, JA
Mauban, JRH
机构
[1] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 278卷 / 06期
关键词
cardiac muscle; fluorescence; excitation-contraction coupling; microscopy;
D O I
10.1152/ajpheart.2000.278.6.H2150
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We describe a custom one-photon (confocal) and two-photon all-digital (photon counting) laser scanning microscope. The confocal component uses two avalanche photodiodes (APDs) as the fluorescence detector to achieve high sensitivity and to overcome the limited photon counting rate of a single APD (similar to 5 MHz). The confocal component is approximately nine times more efficient than our commercial confocal microscope (fluorophore fluo 4). Switching from one-photon to two-photon excitation mode (Ti: sapphire laser) is accomplished by moving a single mirror beneath the objective lens. The pulse from the Ti: sapphire laser is 109 fs in duration at the specimen plane, and average power is similar to 5 mW. Two-photon excited fluorescence is detected by a fast photomultiplier tube. With a x63 1.4 NA oil-immersion objective, the resolution of the confocal system is 0.25 mu m laterally and 0.52 mu m axially. For the two-photon system, the corresponding values are 0.28 and 0.82 mu m. The system is advantageous when excitation intensity must be limited, when fluorescence is low, or when thick, scattering specimens are being studied (with two-photon excitation).
引用
收藏
页码:H2150 / H2156
页数:7
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