Abstract
The use of light polarization properties in the analysis of fluorescence images has driven a large amount of research toward the measurement of orientational behavior of molecules in cells, in particular in their membranes. This field has been recently revisited to enlarge the possibilities of polarization-resolved fluorescence microscopy. We show that this technique allows retrieving a wealth of information on the constraints that hinder rotational mobility of lipid probes and proteins in membranes, bringing thus new insights on inter-proteins and lipid-protein interactions, on membrane morphology at the sub-diffraction length scale and on local membrane physical properties such as viscosity.
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Acknowledgements
The authors thank H. Rigneault, P. Réfrégier, and J. Duboisset (Institut Fresnel, Marseille, France), as well as D. Marguet, H.T. He, and T. Trombik (Centre d’Immunologie de Marseille Luminy, Marseille, France), for helpful discussions and advices. The Institut Fresnel work mentioned in this chapter was supported by CNRS, Agence Nationale de la Recherche, the region Provence Alpes Côte d’Azur.
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Brasselet, S., Ferrand, P., Kress, A., Wang, X., Ranchon, H., Gasecka, A. (2012). Imaging Molecular Order in Cell Membranes by Polarization-Resolved Fluorescence Microscopy. In: Mély, Y., Duportail, G. (eds) Fluorescent Methods to Study Biological Membranes. Springer Series on Fluorescence, vol 13. Springer, Berlin, Heidelberg. https://doi.org/10.1007/4243_2012_51
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DOI: https://doi.org/10.1007/4243_2012_51
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