Principles of two-photon excitation fluorescence microscopy and other nonlinear imaging approaches

被引:174
|
作者
Oheim, Martin
Michael, Darren J.
Geisbauer, Matthias
Madsen, Dorte
Chow, Robert H.
机构
[1] INSERM, U603, Lab Neurophysiol & New Microscopies, F-75006 Paris, France
[2] Univ So Calif, Keck Med Sch, Zilkha Neurogenet Inst, Los Angeles, CA 90089 USA
[3] Univ So Calif, Keck Med Sch, Dept Physiol & Biophys, Los Angeles, CA 90089 USA
关键词
two-photon excitation fluorescence (2PEF) microscopy; coherent anti-Stokes Raman scattering; planar 2PEF microscopy;
D O I
10.1016/j.addr.2006.07.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this article is to review the basic principles of two-photon excitation fluorescence (2PEF) microscopy and to compare the advantages and disadvantages of 2PEF imaging to other microscopy methodologies. 2PEF imaging is a nonlinear approach that generates images, of optical sections and that is particularly well suited for deep-tissue and in vivo imaging of live animals. The nonlinear excitation used for 2PEF offers the advantage, too, of being able to generate contrast from second or third harmonic generation as well as coherent anti-Stokes Raman scattering. We also review the recent use of nonlinear excitation to provide image resolution beyond the diffraction limit and discuss the progress in non-scanning (planar) 2PEF microscopy, an approach that holds great potential for large-scale quantitative imaging and plate reading, e.g., in screening applications. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:788 / 808
页数:21
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