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The orientation of transition moments of dye molecules used in fluorescence studies of muscle systems

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Abstract

Fluorescence and phosphorescence depolarization techniques can provide information on orientational order and rotational motion of crossbridges in muscle fibres. However the depolarization experiment monitors the orientation and motion of the crossbridges indirectly. The changes in depolarization arise from a change in the orientation of the transition dipoles of the dye attached to the crossbridge. In order to extract the physiologically relevant orientations from the data it is therefore necessary to characterize the orientation of the dye molecule relative to the crossbridge and the orientation of the transition moments in the frame of the dyes. The dyes 1,5-1-AEDANS and eosin-5-maleimide are commonly used for labelling the crossbridge in muscle fibres. The orientations of the absorption and fluorescence emission dipoles of these two dyes in the molecular frame were determined. Angle resolved fluorescence depolarization experiments on the dyes, macroscopically aligned in a stretched polymer matrix of poly vinyl alcohol, were carried out. The data were analyzed in terms of an orientational distribution of the dye molecules in the film and the orientations of the absorption and emission dipoles in the frame of the dye molecule. Experimental data, obtained from a given sample at different excitation wavelengths, were analyzed simultaneously in a global target approach. This leads to a reduction in the number of independent parameters optimized by the non-linear least squares procedure.

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Abbreviations

1,5-I-AEDANS:

5-iodoacetamido-ethyl-aminonaphthalene-a-sulfonic acid

IATR:

iodoacetamido-tetra-methylrhodamine

E5M:

Eosin-5-Maleimide

ATP:

adenosine tri phosphate

ɛ-ATP:

1:N6-ethano-ATP

ɛ-2-aza-ATP:

1:N6-etheno-2-aza-ATP

ant-ATP:

anthraniloyl-ATP

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van der Heide, U.A., Orbons, B., Gerritsen, H.C. et al. The orientation of transition moments of dye molecules used in fluorescence studies of muscle systems. Eur Biophys J 21, 263–272 (1992). https://doi.org/10.1007/BF00185121

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  • DOI: https://doi.org/10.1007/BF00185121

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