Literature DB >> 34214540

Light scattering in TIRF microscopy: A theoretical study of the limits to surface selectivity.

Jeremy J Axelrod1, Daniel Axelrod2.   

Abstract

In TIRF microscopy, the sample resides near a surface in an evanescent optical field that, ideally, decreases in intensity with distance from the surface in a pure exponential fashion. In practice, multiple surfaces and imperfections in the optical system and refractive index (RI) inhomogeneities in the sample (often living cells) produce propagating scattered light that degrades the exponential purity. RI inhomogeneities cannot easily be avoided. How severe is the consequent optical degradation? Starting from Maxwell's equations, we derive a first-order perturbative approximation of the electric field strength of light scattered by sample RI inhomogeneities of several types under coherent evanescent field illumination. The approximation provides an expression for the scattering field of any arbitrary RI inhomogeneity pattern. The scattering is not all propagating; some is evanescent and remains near the scattering centers. The results presented here are only a first-order approximation, and they ignore multiple scattering and reflections off the total internal reflection (TIR) surface. For simplicity, we assume that the RI variations in the z direction are insignificant within the depth of the evanescent field and consider only scattering of excitation light, not fluorescence emission light. The general conclusion of most significance from this study is that TIR scattering from a sample with RI variations typical of those on a cell culture alters the effective thickness of the illumination to only ∼50% greater than it would be without scattering. The qualitative surface selectivity of TIR fluorescence is largely retained even in the presence of scattering. Quantitatively, however, scattering will cause a deviation from the incident exponential decay at shorter distances, adding a slower decaying background. Calculations that assume a pure exponential decay will be approximations, and scattering should be taken into account. TIR scattering is only slightly dependent on polarization but is strongly reduced for the highest accessible incidence angles.
Copyright © 2021 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2021        PMID: 34214540      PMCID: PMC8391032          DOI: 10.1016/j.bpj.2021.06.025

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   3.699


  25 in total

1.  A surface contact microscope for the study of cell movements.

Authors:  E J AMBROSE
Journal:  Nature       Date:  1956-11-24       Impact factor: 49.962

2.  Effective elimination of laser interference fringing in fluorescence microscopy by spinning azimuthal incidence angle.

Authors:  Alexa L Mattheyses; Keith Shaw; Daniel Axelrod
Journal:  Microsc Res Tech       Date:  2006-08       Impact factor: 2.769

3.  Coherent total internal reflection dark-field microscopy: label-free imaging beyond the diffraction limit.

Authors:  Philipp von Olshausen; Alexander Rohrbach
Journal:  Opt Lett       Date:  2013-10-15       Impact factor: 3.776

4.  Visualizing Intracellular Organelle and Cytoskeletal Interactions at Nanoscale Resolution on Millisecond Timescales.

Authors:  Yuting Guo; Di Li; Siwei Zhang; Yanrui Yang; Jia-Jia Liu; Xinyu Wang; Chong Liu; Daniel E Milkie; Regan P Moore; U Serdar Tulu; Daniel P Kiehart; Junjie Hu; Jennifer Lippincott-Schwartz; Eric Betzig; Dong Li
Journal:  Cell       Date:  2018-10-25       Impact factor: 41.582

5.  Full-field near-field optical microscope for cell imaging.

Authors:  Thomas Barroca; Karla Balaa; Sandrine Lévêque-Fort; Emmanuel Fort
Journal:  Phys Rev Lett       Date:  2012-05-22       Impact factor: 9.161

Review 6.  Evanescent excitation and emission in fluorescence microscopy.

Authors:  Daniel Axelrod
Journal:  Biophys J       Date:  2013-04-02       Impact factor: 4.033

7.  Eliminating unwanted far-field excitation in objective-type TIRF. Part II. combined evanescent-wave excitation and supercritical-angle fluorescence detection improves optical sectioning.

Authors:  Maia Brunstein; Karine Hérault; Martin Oheim
Journal:  Biophys J       Date:  2014-03-04       Impact factor: 4.033

8.  Eliminating unwanted far-field excitation in objective-type TIRF. Part I. identifying sources of nonevanescent excitation light.

Authors:  Maia Brunstein; Maxime Teremetz; Karine Hérault; Christophe Tourain; Martin Oheim
Journal:  Biophys J       Date:  2014-03-04       Impact factor: 4.033

9.  Refractive Index Imaging of Cells with Variable-Angle Near-Total Internal Reflection (TIR) Microscopy.

Authors:  Kevin P Bohannon; Ronald W Holz; Daniel Axelrod
Journal:  Microsc Microanal       Date:  2017-09-18       Impact factor: 4.127

10.  Measuring surface dynamics of biomolecules by total internal reflection fluorescence with photobleaching recovery or correlation spectroscopy.

Authors:  N L Thompson; T P Burghardt; D Axelrod
Journal:  Biophys J       Date:  1981-03       Impact factor: 4.033

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  2 in total

1.  Optometry for a short-sighted microscope.

Authors:  Carine Julien; Martin Oheim
Journal:  Biophys J       Date:  2021-09-10       Impact factor: 3.699

2.  VAMP2 and synaptotagmin mobility in chromaffin granule membranes: implications for regulated exocytosis.

Authors:  Prabhodh S Abbineni; Joseph S Briguglio; Edwin R Chapman; Ronald W Holz; Daniel Axelrod
Journal:  Mol Biol Cell       Date:  2021-12-01       Impact factor: 3.612

  2 in total

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