Photobleaching in two-photon excitation microscopy

被引:414
|
作者
Patterson, GH [1 ]
Piston, DW [1 ]
机构
[1] Vanderbilt Univ, Dept Physiol & Mol Biophys, Nashville, TN 37232 USA
关键词
D O I
10.1016/S0006-3495(00)76762-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The intensity-squared dependence of two-photon excitation in laser scanning microscopy restricts excitation to the focal plane and leads to decreased photobleaching in thick samples. However, the high photon flux used in these experiments can potentially lead to higher-order photon interactions within the focal volume. The excitation power dependence of the fluorescence intensity and the photobleaching rate of thin fluorescence samples (similar to 1 mu m) were examined under one- and two-photon excitation. As expected, log-log plots of excitation power Versus the fluorescence intensity and photobleaching rate for one-photon excitation of fluorescein increased with a slope of similar to 1.A similar plot of the fluorescence intensity Versus two-photon excitation power increased with a slope of similar to 2. However, the two-photon photobleaching rate increased with a slope greater than or equal to 3, indicating the presence of higher-order photon interactions. Similar experiments on Indo-1, NADH, and aminocoumarin produced similar results and suggest that this higher-order photobleaching is common in two-photon excitation microscopy. As a consequence, the use of multi-photon excitation microscopy to study thin samples may be limited by increased photobleaching.
引用
收藏
页码:2159 / 2162
页数:4
相关论文
共 50 条
  • [31] Two-photon fluorescence excitation and related techniques in biological microscopy
    Diaspro, Alberto
    Chirico, Giuseppe
    Collini, Maddalena
    QUARTERLY REVIEWS OF BIOPHYSICS, 2005, 38 (02) : 97 - 166
  • [32] Two-photon microscopy with wavelength switchable fiber laser excitation
    Unruh, Jay R.
    Price, E. Shane
    Molla, Roque Gagliano
    Stehno-Bittel, Lisa
    Johnson, Carey K.
    Hui, Rongqing
    OPTICS EXPRESS, 2006, 14 (21): : 9825 - 9831
  • [33] Principles of two-photon excitation microscopy and its applications to neuroscience
    Svoboda, Karel
    Yasuda, Ryohei
    NEURON, 2006, 50 (06) : 823 - 839
  • [34] More than double the fun with two-photon excitation microscopy
    Luu, Peter
    Fraser, Scott E.
    Schneider, Falk
    COMMUNICATIONS BIOLOGY, 2024, 7 (01)
  • [35] Two-photon excitation microscopy of tryptophan-containing proteins
    Lippitz, M
    Erker, W
    Decker, H
    van Holde, KE
    Basché, T
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) : 2772 - 2777
  • [36] Optimizing Fluorescence Excitation and Detection for Intravital Two-Photon Microscopy
    Suan, Dan
    Hampton, Henry R.
    Tomura, Michio
    Kanagawa, Osami
    Chtanova, Tatyana
    Tri Giang Phan
    LABORATORY METHODS IN CELL BIOLOGY: IMAGING, 2012, 113 : 311 - 323
  • [37] Nanoshells for in vivo imaging using two-photon excitation microscopy
    Gao, Liang
    Vadakkan, Tegy J.
    Nammalvar, Vengadesan
    NANOTECHNOLOGY, 2011, 22 (36)
  • [38] Soft computing approach to confocal and two-photon excitation microscopy
    Vicidomini, Giuseppe
    Mondal, Partha P.
    Diaspro, Alberto
    THREE-DIMENSIONAL AND MULTIDIMENSIONAL MICROSCOPY: IMAGE ACQUISITION AND PROCESSING XIV, 2007, 6443
  • [39] Assessment of Cerebral Tumors and Metastases by Two-Photon Excitation Microscopy
    Enache, Adrian
    Eftimie, Lucian G.
    Graur, Ana M.
    Glogojeanu, Remus R.
    Geambasu, Adina
    Voinea, Oana C.
    Costache, Daniel O.
    Costache, Raluca S.
    Sajin, Maria
    Stanciu, George A.
    ROMANIAN JOURNAL OF MILITARY MEDICINE, 2023, 126 (04) : 418 - 423
  • [40] Imaging living cells and tissues by two-photon excitation microscopy
    Piston, DW
    TRENDS IN CELL BIOLOGY, 1999, 9 (02) : 66 - 69