The orientation of eosin-5-maleimide on human erythrocyte band 3 measured by fluorescence polarization microscopy.

Blackman SM, Cobb CE, Beth AH, Piston DW
Biophys J. 1996 71 (1): 194-208

PMID: 8804603 · PMCID: PMC1233471 · DOI:10.1016/S0006-3495(96)79216-0

The dominant motional mode for membrane proteins is uniaxial rotational diffusion about the membrane normal axis, and investigations of their rotational dynamics can yield insight into both the oligomeric state of the protein and its interactions with other proteins such as the cytoskeleton. However, results from the spectroscopic methods used to study these dynamics are dependent on the orientation of the probe relative to the axis of motion. We have employed polarized fluorescence confocal microscopy to measure the orientation of eosin-5-maleimide covalently reacted with Lys-430 of human erythrocyte band 3. Steady-state polarized fluorescence images showed distinct intensity patterns, which were fit to an orientation distribution of the eosin absorption and emission dipoles relative to the membrane normal axis. This orientation was found to be unchanged by trypsin treatment, which cleaves band 3 between the integral membrane domain and the cytoskeleton-attached domain. this result suggests that phosphorescence anisotropy changes observed after trypsin treatment are due to a rotational constraint change rather than a reorientation of eosin. By coupling time-resolved prompt fluorescence anisotropy with confocal microscopy, we calculated the expected amplitudes of the e-Dt and e-4Dt terms from the uniaxial rotational diffusion model and found that the e-4Dt term should dominate the anisotropy decay. Delayed fluorescence and phosphorescence anisotropy decays of control and trypsin-treated band 3 in ghosts, analyzed as multiple uniaxially rotating populations using the amplitudes predicted by confocal microscopy, were consistent with three motional species with uniaxial correlation times ranging from 7 microseconds to 1.4 ms.

MeSH Terms (16)

Anion Exchange Protein 1, Erythrocyte Biophysical Phenomena Biophysics Diffusion Electron Spin Resonance Spectroscopy Eosine Yellowish-(YS) Erythrocyte Membrane Fluorescence Polarization Fluorescent Dyes Humans Microscopy, Confocal Microscopy, Fluorescence Models, Chemical Rotation Thermodynamics Trypsin

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