Multi-photon excitation microscopy

被引:122
作者
Diaspro, Alberto
Bianchini, Paolo
Vicidomini, Giuseppe
Faretta, Mario
Ramoino, Paola
Usai, Cesare
机构
[1] Univ Genoa, Dept Phys, LAMBS MicroScoBio Res Ctr, I-16146 Genoa, Italy
[2] IFOM, FIRC Inst Mol Oncol Fdn, I-20139 Milan, Italy
[3] European Inst Oncol, IFOM IEO Consortium Oncogenom, I-20141 Milan, Italy
[4] Univ Genoa, DIPTERIS Dept Study Terr & Resources, I-16132 Genoa, Italy
[5] CNR, Inst Biophys, I-16149 Genoa, Italy
关键词
D O I
10.1186/1475-925X-5-36
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Multi-photon excitation (MPE) microscopy plays a growing role among microscopical techniques utilized for studying biological matter. In conjunction with confocal microscopy it can be considered the imaging workhorse of life science laboratories. Its roots can be found in a fundamental work written by Maria Goeppert Mayer more than 70 years ago. Nowadays, 2PE and MPE microscopes are expected to increase their impact in areas such biotechnology, neurobiology, embryology, tissue engineering, materials science where imaging can be coupled to the possibility of using the microscopes in an active way, too. As well, 2PE implementations in noninvasive optical bioscopy or laser-based treatments point out to the relevance in clinical applications. Here we report about some basic aspects related to the phenomenon, implications in three-dimensional imaging microscopy, practical aspects related to design and realization of MPE microscopes, and we only give a list of potential applications and variations on the theme in order to offer a starting point for advancing new applications and developments.
引用
收藏
页数:14
相关论文
共 59 条
  • [1] Dimethyl-pepep: a DNA probe in two-photon excitation cellular imaging
    Abbotto, A
    Baldini, G
    Beverina, L
    Chirico, G
    Collini, M
    D'Alfonso, L
    Diaspro, A
    Magrassi, R
    Nardo, L
    Pagani, GA
    [J]. BIOPHYSICAL CHEMISTRY, 2005, 114 (01) : 35 - 41
  • [2] Lessons from the history of light microscopy
    Amos, B
    [J]. NATURE CELL BIOLOGY, 2000, 2 (08) : E151 - E152
  • [3] How the Confocal Laser Scanning Microscope entered Biological Research
    Amos, WB
    White, JG
    [J]. BIOLOGY OF THE CELL, 2003, 95 (06) : 335 - 342
  • [4] FLUORESCENCE DIGITAL IMAGING MICROSCOPY IN CELL BIOLOGY
    ARNDTJOVIN, DJ
    ROBERTNICOUD, M
    KAUFMAN, SJ
    JOVIN, TM
    [J]. SCIENCE, 1985, 230 (4723) : 247 - 256
  • [5] Metal-enhanced fluorescence: an emerging tool in biotechnology
    Aslan, K
    Gryczynski, I
    Malicka, J
    Matveeva, E
    Lakowicz, JR
    Geddes, CD
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 2005, 16 (01) : 55 - 62
  • [6] Light microscopy on the move - Introduction
    Bastiaens, PIH
    Hell, SW
    [J]. JOURNAL OF STRUCTURAL BIOLOGY, 2004, 147 (01) : 1 - 2
  • [7] Properties of crosslinked protein matrices for tissue engineering applications synthesized by multiphoton excitation
    Basu, S
    Campagnola, PJ
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 71A (02) : 359 - 368
  • [8] BELTRAME F, 1985, NATO ASI SER, V97, P483
  • [9] POSSIBLE 2-PHOTON EFFECT INVITRO USING A FOCUSED LASER-BEAM
    BERNS, MW
    [J]. BIOPHYSICAL JOURNAL, 1976, 16 (08) : 973 - 977
  • [10] Bhawalkar J D, 1997, J Clin Laser Med Surg, V15, P201