Literature DB >> 24108641

Time-resolved fluorescence anisotropy imaging.

Klaus Suhling1, James Levitt, Pei-Hua Chung.   

Abstract

Fluorescence can be characterized by its intensity, position, wavelength, lifetime, and polarization. The more of these features are acquired in a single measurement, the more can be learned about the sample, i.e., the microenvironment of the fluorescence probe. Polarization-resolved fluorescence lifetime imaging-time-resolved fluorescence anisotropy imaging, TR-FAIM-allows mapping of viscosity or binding or of homo-FRET which can indicate dimerization or generally oligomerization.

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Year:  2014        PMID: 24108641     DOI: 10.1007/978-1-62703-649-8_22

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Physical properties of the cytoplasm modulate the rates of microtubule polymerization and depolymerization.

Authors:  Arthur T Molines; Joël Lemière; Morgan Gazzola; Ida Emilie Steinmark; Claire H Edrington; Chieh-Ting Hsu; Paula Real-Calderon; Klaus Suhling; Gohta Goshima; Liam J Holt; Manuel Thery; Gary J Brouhard; Fred Chang
Journal:  Dev Cell       Date:  2022-02-28       Impact factor: 13.417

2.  Total internal reflection fluorescence anisotropy imaging microscopy: setup, calibration, and data processing for protein polymerization measurements in living cells.

Authors:  Florian Ströhl; Hovy H W Wong; Christine E Holt; Clemens F Kaminski
Journal:  Methods Appl Fluoresc       Date:  2017-12-19       Impact factor: 3.009

3.  Hydrodynamic Radii of Ranibizumab, Aflibercept and Bevacizumab Measured by Time-Resolved Phosphorescence Anisotropy.

Authors:  Liisa M Hirvonen; Gilbert O Fruhwirth; Nishanthan Srikantha; Matthew J Barber; James E Neffendorf; Klaus Suhling; Timothy L Jackson
Journal:  Pharm Res       Date:  2016-05-25       Impact factor: 4.200

  3 in total

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