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
相关论文
共 50 条
  • [41] Two-photon excitation fluorescence bioassays
    Hanninen, Pekka
    Soukka, Jori
    Soini, Juhani T.
    FLUORESCENCE METHODS AND APPLICATIONS: SPECTROSCOPY, IMAGING, AND PROBES, 2008, 1130 : 320 - 326
  • [42] Fluorescence excitation volume in two-photon microscopy by autocorrelation spectroscopy and photon counting histogram
    Chirico, G
    Olivini, F
    Beretta, S
    APPLIED SPECTROSCOPY, 2000, 54 (07) : 1084 - 1090
  • [43] Two-Photon Fluorescence Imaging
    Feng, Fan
    Mao, Heng
    Wang, Aimin
    Chen, Liangyi
    OPTICAL IMAGING IN HUMAN DISEASE AND BIOLOGICAL RESEARCH, 2021, 1355 : 45 - 61
  • [44] Cell imaging with squaraine dye based on two-photon excitation fluorescence imaging
    Geng, Junxian
    Yi, Rongxing
    Qu, Junle
    Liu, Liwei
    TENTH INTERNATIONAL CONFERENCE ON INFORMATION OPTICS AND PHOTONICS, 2018, 10964
  • [45] Two-photon excitation fluorescence lifetime imaging microscopy: A promising diagnostic tool for digestive tract tumors
    Li, Hui
    Yu, Jia
    Zhang, Rongli
    Li, Xi
    Zheng, Wei
    JOURNAL OF INNOVATIVE OPTICAL HEALTH SCIENCES, 2019, 12 (05)
  • [46] An evaluation of two-photon excitation versus confocal and digital deconvolution fluorescence microscopy imaging in Xenopus morphogenesis
    Periasamy, A
    Skoglund, P
    Noakes, C
    Keller, R
    MICROSCOPY RESEARCH AND TECHNIQUE, 1999, 47 (03) : 172 - 181
  • [47] Improving two-photon excitation microscopy for sharper and faster biological imaging
    Otomo, Kohei
    Ishii, Hirokazu
    Nemoto, Tomomi
    BIOPHYSICS AND PHYSICOBIOLOGY, 2023, 20 (01)
  • [48] Imaging of optically thick specimen using two-photon excitation microscopy
    Gerritsen, HC
    De Grauw, CJ
    MICROSCOPY RESEARCH AND TECHNIQUE, 1999, 47 (03) : 206 - 209
  • [49] Multicolor excitation two-photon microscopy: in vivo imaging of cells and tissues
    Li, Dong
    Zheng, Wei
    Qu, Jianan Y.
    MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES X, 2010, 7569
  • [50] Imaging of optically thick specimen using two-photon excitation microscopy
    Debye Institute, Utrecht University, 3508 TA Utrecht, Netherlands
    不详
    Microsc. Res. Tech., 3 (206-209):