Time-gated total internal reflection fluorescence microscopy with a supercontinuum excitation source

被引:21
作者
Blandin, Pierre [1 ,2 ]
Leveque-Fort, Sandrine [1 ,2 ]
Lecart, Sandrine [2 ]
Cossec, Jack C. [3 ]
Potier, Mane-Claude [3 ]
Lenkei, Zsolt [3 ]
Druon, Frederic [2 ,4 ]
Georges, Patrick [2 ,4 ]
机构
[1] Univ Paris 11, CNRS, Photophys Mol Lab, F-91405 Orsay, France
[2] Univ Paris 11, Ctr Laser, Ctr Photon Biomed, F-91405 Orsay, France
[3] Ecole Super Phys & Chim Ind Ville Paris, CNRS, Lab Neurobiol & Diversite Cellulaire, F-75013 Paris, France
[4] Univ Paris 11, CNRS, Inst Opt, Lab Charles Fabry, F-91127 Palaiseau, France
关键词
AMYLOID PRECURSOR PROTEIN; LIFETIME; ANISOTROPY; IMPACT;
D O I
10.1364/AO.48.000553
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present the instrumental development of a versatile total internal reflection fluorescence lifetime imaging microscopy setup illuminated by a supercontinuum laser source. It enables performing wide-field fluorescence lifetime. imaging with subwavelength axial resolution for a large range of fluorophores. The short overall acquisition time and the axial resolution are well suited for dynamic neurobiological applications. (C) 2009 Optical Society of America
引用
收藏
页码:553 / 559
页数:7
相关论文
共 27 条
[1]   Stimulated emission depletion microscopy with a supercontinuum source and fluorescence lifetime imaging [J].
Auksorius, Egidijus ;
Boruah, Bosanta R. ;
Dunsby, Christopher ;
Lanigan, Peter M. P. ;
Kennedy, Gordon ;
Neil, Mark A. A. ;
French, Paul M. W. .
OPTICS LETTERS, 2008, 33 (02) :113-115
[2]   CELL-SUBSTRATE CONTACTS ILLUMINATED BY TOTAL INTERNAL-REFLECTION FLUORESCENCE [J].
AXELROD, D .
JOURNAL OF CELL BIOLOGY, 1981, 89 (01) :141-145
[3]   Selective imaging of surface fluorescence with very high aperture microscope objectives [J].
Axelrod, D .
JOURNAL OF BIOMEDICAL OPTICS, 2001, 6 (01) :6-13
[4]   Total internal reflection fluorescence microscopy in cell biology [J].
Axelrod, D .
TRAFFIC, 2001, 2 (11) :764-774
[5]   Fluorescence lifetime imaging by time-correlated single-photon counting [J].
Becker, W ;
Bergmann, A ;
Hink, MA ;
König, K ;
Benndorf, K ;
Biskup, C .
MICROSCOPY RESEARCH AND TECHNIQUE, 2004, 63 (01) :58-66
[6]   Application of total internal reflection fluorescence microscopy to study cell adhesion to biomaterials [J].
Burmeister, JS ;
Olivier, LA ;
Reichert, WM ;
Truskey, GA .
BIOMATERIALS, 1998, 19 (4-5) :307-325
[7]   Characterization of two-photon excitation fluorescence lifetime imaging microscopy for protein localization [J].
Chen, YE ;
Periasamy, A .
MICROSCOPY RESEARCH AND TECHNIQUE, 2004, 63 (01) :72-80
[8]   Time-resolved evanescent wave-induced fluorescence anisotropy for the determination of molecular conformational changes of proteins at an interface [J].
Gee, ML ;
Lensun, L ;
Smith, TA ;
Scholes, CA .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2004, 33 (02) :130-139
[9]  
Herman P., 2003, BIOMED PHOTONICS
[10]   Direct measurement of the evanescent-wave polarization state [J].
Jozefowski, Leszek ;
Fiutowski, Jacek ;
Kawalec, Tomasz ;
Rubahn, Horst-Guenter .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 2007, 24 (03) :624-628