Total internal reflection fluorescence microscope

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(Cis-)total internal reflection fluorescence microscope (TIRFM) diagram
  1. Specimen
  2. Evanescent wave range
  3. Cover slip
  4. Immersion oil
  5. Objective
  6. Emission beam (signal)
  7. Excitation beam
(Trans-)total internal reflection fluorescence microscope (TIRFM) diagram
  1. Objective
  2. Emission beam (signal)
  3. Immersion oil
  4. Cover slip
  5. Specimen
  6. Evanescent wave range
  7. Excitation beam
  8. Quartz prism

A total internal reflection fluorescence microscope (TIRFM) is a type of microscope with which a thin region of a specimen, usually less than 200 nm can be observed.

Background[edit]

In cell and molecular biology, a large number of molecular events in cellular surfaces such as cell adhesion, binding of cells by hormones, secretion of neurotransmitters, and membrane dynamics have been studied with conventional fluorescence microscopes. However, fluorophores that are bound to the specimen surface and those in the surrounding medium exist in an equilibrium state. When these molecules are excited and detected with a conventional fluorescence microscope, the resulting fluorescence from those fluorophores bound to the surface is often overwhelmed by the background fluorescence due to the much larger population of non-bound molecules.

Overview[edit]

The idea of using total internal reflection to illuminate cells contacting the surface of glass was first described by E.J. Ambrose in 1956.[1] This idea was then extended by Daniel Axelrod[2] at the University of Michigan, Ann Arbor in the early 1980s as TIRFM. A TIRFM uses an evanescent wave to selectively illuminate and excite fluorophores in a restricted region of the specimen immediately adjacent to the glass-water interface. The evanescent wave is generated only when the incident light is totally internally reflected at the glass-water interface. The evanescent electromagnetic field decays exponentially from the interface, and thus penetrates to a depth of only approximately 100 nm into the sample medium. Thus the TIRFM enables a selective visualization of surface regions such as the basal plasma membrane (which are about 7.5 nm thick) of cells as shown in the figure above. Note, however, that the region visualised is at least a few hundred nanometers wide, so the cytoplasmic zone immediately beneath the plasma membrane is necessarily visualised in addition to the plasma membrane during TIRF microscopy. The selective visualisation of the plasma membrane renders the features and events on the plasma membrane in living cells with high axial resolution.

TIRF can also be used to observe the fluorescence of a single molecule,[3][4] making it an important tool of biophysics and quantitative biology.

References[edit]

  1. ^ Ambrose, EJ (24 Nov 1956). "A surface contact microscope for the study of cell movements.". Nature. 178(4543) (4543): 1194. Bibcode:1956Natur.178.1194A. doi:10.1038/1781194a0. 
  2. ^ Axelrod, D. (1 April 1981). "Cell-substrate contacts illuminated by total internal reflection fluorescence". The Journal of Cell Biology 89 (1): 141–145. doi:10.1083/jcb.89.1.141. PMC 2111781. PMID 7014571. Retrieved 16 January 2012. 
  3. ^ Yanagida, Toshio; Sako, Yasushi, Minoghchi, Shigeru (10 February 2000). "Single-molecule imaging of EGFR signalling on the surface of living cells". Nature Cell Biology 2 (3): 168–172. doi:10.1038/35004044. 
  4. ^ Andre et al. Cross-correlated tirf/afm reveals asymmetric distribution of forcegenerating heads along self-assembled, synthetic myosin filaments. Biophysical Journal, 96:1952–1960, 2009.
  • Axelrod, Daniel (1 November 2001). "Total Internal Reflection Fluorescence Microscopy in Cell Biology". Traffic 2 (11): 764–774. doi:10.1034/j.1600-0854.2001.21104.x. 

External links[edit]