Literature DB >> 23208218

Measuring incidence angle for through-the-objective total internal reflection fluorescence microscopy.

Thomas P Burghardt1.   

Abstract

Total internal reflection fluorescence (TIRF) microscopy has the exciting laser beam incident beyond critical angle from the glass side of a glass/aqueous interface formed by the coverslip and aqueous sample. The aqueous side evanescent field decays exponentially with distance from the interface with penetration depth depending on incidence angle. Through-the-objective TIRF has the exciting laser focused at the back focal plane (BFP) creating a refracted parallel beam approaching the interface in the small gap between objective and coverslip, making incidence angle challenging to measure. Objective axial scanning does not affect incidence angle but translates beam and interface intersection detected by the fluorescence center of mass from fluorescent spheres attached to the aqueous side of the interface. Center of mass translation divided by the axial translation is the tangent of the incidence angle that is sampled repeatedly over objective trajectory to obtain a best estimate. Incidence angle is measured for progressively larger radial positions of the focused beam on the BFP. A through-the-objective TIRF microscope, utilizing a micrometer and relay lenses to position the focused beam at the BFP, is calibrated for incidence angle. Calibration depends on microscope characteristics and TIRF objective and is applicable to any interface or sample.

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Year:  2012        PMID: 23208218      PMCID: PMC3512109          DOI: 10.1117/1.JBO.17.12.126007

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  8 in total

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Authors:  D Axelrod
Journal:  Traffic       Date:  2001-11       Impact factor: 6.215

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Authors:  Atom Sarkar; Ragan B Robertson; Julio M Fernandez
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-23       Impact factor: 11.205

3.  Evanescent field excitation of fluorescence by epi-illumination microscopy.

Authors:  A L Stout; D Axelrod
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4.  Spatially and temporally synchronized atomic force and total internal reflection fluorescence microscopy for imaging and manipulating cells and biomolecules.

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Journal:  Biophys J       Date:  2006-07-21       Impact factor: 4.033

Review 5.  Combinatorial microscopy.

Authors:  Daniel Axelrod; Geneva M Omann
Journal:  Nat Rev Mol Cell Biol       Date:  2006-12       Impact factor: 94.444

6.  Direct measurement of the evanescent field profile produced by objective-based total internal reflection fluorescence.

Authors:  Alexa L Mattheyses; Daniel Axelrod
Journal:  J Biomed Opt       Date:  2006 Jan-Feb       Impact factor: 3.170

7.  Around-the-objective total internal reflection fluorescence microscopy.

Authors:  Thomas P Burghardt; Andrew D Hipp; Katalin Ajtai
Journal:  Appl Opt       Date:  2009-11-10       Impact factor: 1.980

8.  Cell-substrate contacts illuminated by total internal reflection fluorescence.

Authors:  D Axelrod
Journal:  J Cell Biol       Date:  1981-04       Impact factor: 10.539

  8 in total
  4 in total

Review 1.  Calibrating Evanescent-Wave Penetration Depths for Biological TIRF Microscopy.

Authors:  Martin Oheim; Adi Salomon; Adam Weissman; Maia Brunstein; Ute Becherer
Journal:  Biophys J       Date:  2019-08-05       Impact factor: 4.033

2.  DNA-Endonuclease Complex Dynamics by Simultaneous FRET and Fluorophore Intensity in Evanescent Field.

Authors:  Marijonas Tutkus; Tomas Marciulionis; Giedrius Sasnauskas; Danielis Rutkauskas
Journal:  Biophys J       Date:  2017-03-14       Impact factor: 4.033

3.  Combined Magnetic Tweezers and Micro-mirror Total Internal Reflection Fluorescence Microscope for Single-Molecule Manipulation and Visualization.

Authors:  Yeonee Seol; Keir C Neuman
Journal:  Methods Mol Biol       Date:  2018

Review 4.  Total internal reflection fluorescence quantification of receptor pharmacology.

Authors:  Ye Fang
Journal:  Biosensors (Basel)       Date:  2015-04-27
  4 in total

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