help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Biophysical Journal 53: 575-591 (1988)
© 1988 the Biophysical Society

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Velez, M
Right arrow Articles by Axelrod, D
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Velez, M
Right arrow Articles by Axelrod, D

Polarized fluorescence photobleaching recovery for measuring rotational diffusion in solutions and membranes.

M Velez and D Axelrod

Biophysics Research Division, University of Michigan, Ann Arbor 48109.

ABSTRACT

A variation of fluorescence photobleaching recovery (FPR) suitable for measuring the rate of rotational molecular diffusion in solution and cell membranes is presented in theory and experimental practice for epi-illumination microscopy. In this technique, a brief flash of polarized laser light creates an anisotropic distribution of unbleached fluorophores which relaxes by rotational diffusion, leading to a time-dependent postbleach fluorescence. Polarized FPR (PFPR) is applicable to any time scales from seconds to microseconds. However, at fast (microsecond) time scales, a partial recovery independent of molecular orientation tends to obscure rotational effects. The theory here presents a method for overcoming this reversible photobleaching, and includes explicit results for practical geometries, fast wobble of fluorophores, and arbitrary bleaching depth. This variation of a polarized luminescence "pump-and-probe" technique is compared with prior ones and with "pump-only" time-resolved luminescence anisotropy decay methods. The technique is experimentally verified on small latex beads with a variety of diameters, common fluorophore labels, and solvent viscosities. Preliminary measurements on a protein (acetylcholine receptor) in the membrane of nondeoxygenated cells in live culture (rat myotubes) show a difference in rotational diffusion between clustered and nonclustered receptors. In most experiments, signal averaging, high laser power, and automated sample translation must be employed to achieve adequate statistical accuracy.




This article has been cited by other articles:


Home page
Biophys. JHome page
J. V. Rocheleau, M. Edidin, and D. W. Piston
Intrasequence GFP in Class I MHC Molecules, a Rigid Probe for Fluorescence Anisotropy Measurements of the Membrane Environment
Biophys. J., June 1, 2003; 84(6): 4078 - 4086.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
J. R. Abney, B. Cutler, M. L. Fillbach, D. Axelrod, and B. A. Scalettar
Chromatin Dynamics in Interphase Nuclei and Its Implications for Nuclear Structure
J. Cell Biol., June 30, 1997; 137(7): 1459 - 1468.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 by the Biophysical Society.