Interpretation of the Spatial Charge Displacements in Bacteriorhodopsin in Terms of Structural Changes during the Photocycle

We have recently introduced a method, made possible by an improved orienting technique using a combination of electric and magnetic fields, that allows the three-dimensional detection of the intramolecular charge displacements during the photocycle of bacteriorhodopsin. This method generates electri...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1999-03, Vol.96 (6), p.2776-2781
Hauptverfasser: Dér, András, Oroszi, László, Kulcsár, Agnes, Zimányi, László, Tóth-Boconádi, Rudolf, Keszthelyi, Lajos, Stoeckenius, Walther, Ormos, Pál
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Sprache:eng
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Zusammenfassung:We have recently introduced a method, made possible by an improved orienting technique using a combination of electric and magnetic fields, that allows the three-dimensional detection of the intramolecular charge displacements during the photocycle of bacteriorhodopsin. This method generates electric asymmetry, a prerequisite for the detection of electric signal on the macroscopic sample, in all three spatial dimensions. Purple membrane fragments containing bacteriorhodopsin were oriented so that their permanent electric dipole moment vectors were perpendicular to the membrane plane and pointed in the same direction. The resulting cylindrical symmetry was broken by photoselection, i. e., by flash excitation with low intensity linearly polarized light. From the measured electric signals, the three-dimensional motion of the electric charge center in the bacteriorhodopsin molecules was calculated for the first 400 μ s. Simultaneous absorption kinetic recording provided the time-dependent concentrations of the intermediates. Combining the two sets of data, we determined the discrete dipole moments of intermediates up to M. When compared with the results of current molecular dynamics calculations, the data provided a decisive experimental test for selecting the optimal theoretical model for the proton transport and should eventually lead to a full description of the mechanism of the bacteriorhodopsin proton pump.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.96.6.2776