Total Internal Reflection Fluorescence Microscopy

被引:134
作者
Axelrod, Daniel [1 ,2 ]
机构
[1] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biophys, Ann Arbor, MI 48109 USA
来源
BIOPHYSICAL TOOLS FOR BIOLOGISTS, VOL 2: IN VIVO TECHNIQUES | 2008年 / 89卷
关键词
D O I
10.1016/S0091-679X(08)00607-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Total internal reflection fluorescence microscopy (TIRFM), also known as evanescent wave microscopy, is used in a wide range of applications, particularly to view single molecules attached to planar surfaces and to study the position and dynamics of molecules and organelles in living culture cells near the contact regions with the glass coverslip. TIRFM selectively illuminates fluorophores only in a very thin (less than 100 nm deep) layer near the substrate., thereby avoiding excitation of fluorophores outside this subresolution optical section. This chapter reviews the history, Current applications in cell biology and biochemistry, basic optical theory, combinations with numerous other optical and spectroscopic approaches, and a range of setup methods, both commercial and custom.
引用
收藏
页码:169 / 221
页数:53
相关论文
共 184 条
[81]   Real-time measurements of actin filament polymerization by total internal reflection fluorescence microscopy [J].
Kuhn, JR ;
Pollard, TD .
BIOPHYSICAL JOURNAL, 2005, 88 (02) :1387-1402
[82]   Rebinding of IgE Fabs at haptenated planar membranes: Measurement by total internal reflection with fluorescence photobleaching recovery [J].
Lagerholm, BC ;
Starr, TE ;
Volovyk, ZN ;
Thompson, NL .
BIOCHEMISTRY, 2000, 39 (08) :2042-2051
[83]  
Lagerholm BC, 2003, METHOD ENZYMOL, V361, P175
[84]   Radiative decay engineering 5: metal-enhanced fluorescence and plasmon emission [J].
Lakowicz, JR .
ANALYTICAL BIOCHEMISTRY, 2005, 337 (02) :171-194
[85]   Role of actin cortex in the subplasmalemmal transport of secretory granules in PC-12 cells [J].
Lang, T ;
Wacker, I ;
Wunderlich, I ;
Rohrbach, A ;
Giese, G ;
Soldati, T ;
Almers, W .
BIOPHYSICAL JOURNAL, 2000, 78 (06) :2863-2877
[86]   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
[87]   SNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosis [J].
Lang, T ;
Bruns, D ;
Wenzel, D ;
Riedel, D ;
Holroyd, P ;
Thiele, C ;
Jahn, R .
EMBO JOURNAL, 2001, 20 (09) :2202-2213
[88]   Single-molecule orientations determined by direct emission pattern imaging [J].
Lieb, MA ;
Zavislan, JM ;
Novotny, L .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 2004, 21 (06) :1210-1215
[89]   Quantifying axial secretory-granule motion with variable-angle evanescent-field excitation [J].
Loerke, D ;
Stühmer, W ;
Oheim, M .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 119 (01) :65-73
[90]   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