Imaging with total internal reflection fluorescence microscopy for the cell biologist

被引:248
作者
Mattheyses, Alexa L. [2 ]
Simon, Sanford M. [2 ]
Rappoport, Joshua Z. [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[2] Rockefeller Univ, Lab Cellular Biophys, New York, NY 10065 USA
基金
英国生物技术与生命科学研究理事会;
关键词
Total internal reflection fluorescence microscopy; Evanescent wave microscopy; Evanescent field microscopy; Fluorescence; CLATHRIN-MEDIATED ENDOCYTOSIS; POST-GOLGI VESICLES; PLASMA-MEMBRANE; CORRELATION SPECTROSCOPY; LIVING CELLS; EXOCYTOSIS; ACTIN; DYNAMICS; COMPLEX; LOCALIZATION;
D O I
10.1242/jcs.056218
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Total internal reflection fluorescence (TIRF) microscopy can be used in a wide range of cell biological applications, and is particularly well suited to analysis of the localization and dynamics of molecules and events near the plasma membrane. The TIRF excitation field decreases exponentially with distance from the cover slip on which cells are grown. This means that fluorophores close to the cover slip (e.g. within similar to 100 nm) are selectively illuminated, highlighting events that occur within this region. The advantages of using TIRF include the ability to obtain high-contrast images of fluorophores near the plasma membrane, very low background from the bulk of the cell, reduced cellular photodamage and rapid exposure times. In this Commentary, we discuss the applications of TIRF to the study of cell biology, the physical basis of TIRF, experimental setup and troubleshooting.
引用
收藏
页码:3621 / 3628
页数:8
相关论文
共 53 条
[1]   Motion matters: Secretory granule motion adjacent to the plasma membrane and exocytosis [J].
Allersma, MW ;
Bittner, MA ;
Axelrod, D ;
Holz, RW .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (05) :2424-2438
[2]   Visualization of regulated exocytosis with a granule membrane probe using total internal reflection microscopy [J].
Allersma, MW ;
Wang, L ;
Axelrod, D ;
Holz, RW .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (10) :4658-4668
[3]   Localized topological changes of the plasma membrane upon exocytosis visualized by polarized TIRFM [J].
Anantharam, Arun ;
Onoa, Bibiana ;
Edwards, Robert H. ;
Holz, Ronald W. ;
Axelrod, Daniel .
JOURNAL OF CELL BIOLOGY, 2010, 188 (03) :415-428
[4]  
Axelrod D, 2003, METHOD ENZYMOL, V361, P1
[5]   CELL-SUBSTRATE CONTACTS ILLUMINATED BY TOTAL INTERNAL-REFLECTION FLUORESCENCE [J].
AXELROD, D .
JOURNAL OF CELL BIOLOGY, 1981, 89 (01) :141-145
[6]  
AXELROD D, 1989, METHOD CELL BIOL, V30, P245
[7]   Total Internal Reflection Fluorescence Microscopy [J].
Axelrod, Daniel .
BIOPHYSICAL TOOLS FOR BIOLOGISTS, VOL 2: IN VIVO TECHNIQUES, 2008, 89 :169-221
[8]   Cross-Correlated TIRF/AFM Reveals Asymmetric Distribution of Force-Generating Heads along Self-Assembled, "Synthetic" Myosin Filaments [J].
Brown, Andre E. X. ;
Hategan, Alina ;
Safer, Daniel ;
Goldman, Yale E. ;
Discher, Dennis E. .
BIOPHYSICAL JOURNAL, 2009, 96 (05) :1952-1960
[9]   Actin and α-actinin orchestrate the assembly and maturation of nascent adhesions in a myosin II motor-independent manner [J].
Choi, Colin K. ;
Vicente-Manzanares, Miguel ;
Zareno, Jessica ;
Whitmore, Leanna A. ;
Mogilner, Alex ;
Horwitz, Alan Rick .
NATURE CELL BIOLOGY, 2008, 10 (09) :1039-U36
[10]   Quantitative fluorescent speckle Microscopy of cytoskeleton dynamics [J].
Danuser, Gaudenz ;
Waterman-Storer, Clare M. .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2006, 35 :361-387