Literature DB >> 6518253

Effect of planar dielectric interfaces on fluorescence emission and detection. Evanescent excitation with high-aperture collection.

T P Burghardt, N L Thompson.   

Abstract

We consider the effect of planar dielectric interfaces (e.g., solid/liquid) on the fluorescence emission of nearby probes. First, we derive an integral expression for the electric field radiated by an oscillating electric dipole when it is close to a dielectric interface. The electric field depends on the refractive indices of the interface, the orientation of the dipole, the distance from the dipole to the interface, and the position of observation. We numerically calculate the electric field intensity for a dipole on an interface, as a function of observation position. These results are applicable to fluorescent molecules excited by the evanescent field of a totally internally reflected laser beam and thus very close to a solid/liquid interface. Next, we derive an integral expression for the electric field radiated when a second dielectric interface is also close to the fluorescent molecule. We numerically calculate this intensity as observed through the second interface. These results are useful when the fluorescence is collected by a high-aperture microscope objective. Finally, we define and calculate a "dichroic factor," which describes the efficiency of collection, in the two-interface system, of polarized fluorescence. The limit when the first interface is removed is applicable for any high-aperture collection of polarized or unpolarized fluorescence. The limit when the second interface is removed has application in the collection of fluorescence with any aperture from molecules close to a dielectric interface. The results of this paper are required for the interpretation of order parameter measurements on fluorescent probes in supported phospholipid monolayers (Thompson, N.L., H. M. McConnell, and T. P. Burghardt, 1984, Biophys. J., 46:739-747).

Entities:  

Mesh:

Year:  1984        PMID: 6518253      PMCID: PMC1435110          DOI: 10.1016/S0006-3495(84)84071-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  6 in total

1.  Order in supported phospholipid monolayers detected by the dichroism of fluorescence excited with polarized evanescent illumination.

Authors:  N L Thompson; H M McConnell; T P Burhardt
Journal:  Biophys J       Date:  1984-12       Impact factor: 4.033

Review 2.  Total internal reflection fluorescence.

Authors:  D Axelrod; T P Burghardt; N L Thompson
Journal:  Annu Rev Biophys Bioeng       Date:  1984

3.  Cross-bridge orientation in skeletal muscle measured by linear dichroism of an extrinsic chromophore.

Authors:  J Borejdo; O Assulin; T Ando; S Putnam
Journal:  J Mol Biol       Date:  1982-07-05       Impact factor: 5.469

4.  Evidence for cross-bridge order in contraction of glycerinated skeletal muscle.

Authors:  T P Burghardt; T Ando; J Borejdo
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

5.  Immunoglobulin surface-binding kinetics studied by total internal reflection with fluorescence correlation spectroscopy.

Authors:  N L Thompson; D Axelrod
Journal:  Biophys J       Date:  1983-07       Impact factor: 4.033

6.  Carbocyanine dye orientation in red cell membrane studied by microscopic fluorescence polarization.

Authors:  D Axelrod
Journal:  Biophys J       Date:  1979-06       Impact factor: 4.033

  6 in total
  25 in total

1.  Observing secretory granules with a multiangle evanescent wave microscope.

Authors:  A Rohrbach
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

Review 2.  Evanescent-wave microscopy: a new tool to gain insight into the control of transmitter release.

Authors:  M Oheim; D Loerke; R H Chow; W Stühmer
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

3.  Time-resolved evanescent wave-induced fluorescence anisotropy for the determination of molecular conformational changes of proteins at an interface.

Authors:  Michelle L Gee; Levie Lensun; Trevor A Smith; Colin A Scholes
Journal:  Eur Biophys J       Date:  2003-10-28       Impact factor: 1.733

4.  Slow rotational mobilities of antibodies and lipids associated with substrate-supported phospholipid monolayers as measured by polarized fluorescence photobleaching recovery.

Authors:  M M Timbs; N L Thompson
Journal:  Biophys J       Date:  1990-08       Impact factor: 4.033

5.  Linear dichroism of acrylodan-labeled tropomyosin and myosin subfragment 1 bound to actin in myofibrils.

Authors:  D Szczesna; S S Lehrer
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

6.  Application of surface plasmon coupled emission to study of muscle.

Authors:  J Borejdo; Z Gryczynski; N Calander; P Muthu; I Gryczynski
Journal:  Biophys J       Date:  2006-07-14       Impact factor: 4.033

7.  Decreasing photobleaching by silver island films: application to muscle.

Authors:  P Muthu; I Gryczynski; Z Gryczynski; J Talent; I Akopova; K Jain; J Borejdo
Journal:  Anal Biochem       Date:  2007-04-12       Impact factor: 3.365

8.  Probing membrane order and topography in supported lipid bilayers by combined polarized total internal reflection fluorescence-atomic force microscopy.

Authors:  John Oreopoulos; Christopher M Yip
Journal:  Biophys J       Date:  2009-03-04       Impact factor: 4.033

9.  Mapping microscope object polarized emission to the back focal plane pattern.

Authors:  Thomas P Burghardt; Katalin Ajtai
Journal:  J Biomed Opt       Date:  2009 May-Jun       Impact factor: 3.170

10.  Determination of the orientation distribution of adsorbed fluorophores using TIRF. II. Measurements on porphyrin and cytochrome c.

Authors:  M A Bos; J M Kleijn
Journal:  Biophys J       Date:  1995-06       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.