Selective imaging of surface fluorescence with very high aperture microscope objectives

被引:123
作者
Axelrod, D [1 ]
机构
[1] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Div Biophys Res, Ann Arbor, MI 48109 USA
关键词
total internal reflection; evanescent field; near field;
D O I
10.1117/1.1335689
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Three approaches to selective surface fluorescence detection are described. All three of them depend on the use of extremely high numerical aperture (NA) objectives now commercially available (1.45 NA from Zeiss and Olympus and 1.65 NA from Olympus). The first two approaches are elaborations of "prismless" total internal reflection fluorescence (TIRF), one approach with a laser illumination and the second with are lamp illumination. The new higher NA objectives are much more suitable for TIRF work on biological cells in culture than are 1.4 NA objectives previously described for prismless TIRF. The third approach is not TIRF at all. It uses the high aperture objective to selectively gather the emission of fluorophores located close enough to the substrate for their near-field energy to be captured by the substrate. Schematic diagrams, experimental demonstrations, and practical suggestions for all these techniques are provided. (C) 2001 Society of Photo-Optical instrumentation Engineers.
引用
收藏
页码:6 / 13
页数:8
相关论文
共 16 条
[1]  
AXELROD D, 2001, IN PRESS AM PHYSICAL
[2]   Three-dimensional imaging of single molecules solvated in pores of poly(acrylamide) gels [J].
Dickson, RM ;
Norris, DJ ;
Tzeng, YL ;
Moerner, WE .
SCIENCE, 1996, 274 (5289) :966-969
[3]   Simultaneous imaging of individual molecules aligned both parallel and perpendicular to the optic axis [J].
Dickson, RM ;
Norris, DJ ;
Moerner, WE .
PHYSICAL REVIEW LETTERS, 1998, 81 (24) :5322-5325
[4]   Single-molecule fluorescence spectroscopy of enzyme conformational dynamics and cleavage mechanism [J].
Ha, TJ ;
Ting, AY ;
Liang, J ;
Caldwell, WB ;
Deniz, AA ;
Chemla, DS ;
Schultz, PG ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :893-898
[5]   Neuropeptide release by efficient recruitment of diffusing cytoplasmic secretory vesicles [J].
Han, WP ;
Ng, YK ;
Axelrod, D ;
Levitan, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14577-14582
[6]   FLUORESCENCE EMISSION AT DIELECTRIC AND METAL-FILM INTERFACES [J].
HELLEN, EH ;
AXELROD, D .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1987, 4 (03) :337-350
[7]   Ca2+-triggered peptide secretion neurotechnique in single cells imaged with green fluorescent protein and evanescent-wave microscopy [J].
Lang, T ;
Wacker, I ;
Steyer, J ;
Kaether, C ;
Wunderlich, I ;
Soldati, T ;
Gerdes, HH ;
Almers, W .
NEURON, 1997, 18 (06) :857-863
[8]   Super-resolution measurements with evanescent-wave fluorescence excitation using variable beam incidence [J].
Loerke, D ;
Preitz, B ;
Stühmer, W ;
Oheim, M .
JOURNAL OF BIOMEDICAL OPTICS, 2000, 5 (01) :23-30
[9]   The last few milliseconds in the life of a secretory granule -: Docking, dynamics and fusion visualized by total internal reflection fluorescence microscopy (TIRFM) [J].
Oheim, M ;
Loerke, D ;
Stühmer, W ;
Chow, RH .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1998, 27 (02) :83-98
[10]   Multiple stimulation dependent processes regulate the size of the releasable pool of vesicles [J].
Oheim, M ;
Loerke, D ;
Stühmer, W ;
Chow, RH .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1999, 28 (02) :91-101