| Literature DB >> 26972111 |
Richard Börner1, Nicky Ehrlich2, Johannes Hohlbein3,4, Christian G Hübner5.
Abstract
Interactions between single molecules profoundly depend on their mutual three-dimensional orientation. Recently, we demonstrated a technique that allows for orientation determination of single dipole emitters using a polarization-resolved distribution of fluorescence into several detection channels. As the method is based on the detection of single photons, it additionally allows for performing fluorescence correlation spectroscopy (FCS) as well as dynamical anisotropy measurements thereby providing access to fast orientational dynamics down to the nanosecond time scale. The 3D orientation is particularly interesting in non-isotropic environments such as lipid membranes, which are of great importance in biology. We used giant unilamellar vesicles (GUVs) labeled with fluorescent dyes down to a single molecule concentration as a model system for both, assessing the robustness of the orientation determination at different timescales and quantifying the associated errors. The vesicles provide a well-defined spherical surface, such that the use of fluorescent lipid dyes (DiO) allows to establish a a wide range of dipole orientations experimentally. To complement our experimental data, we performed Monte Carlo simulations of the rotational dynamics of dipoles incorporated into lipid membranes. Our study offers a comprehensive view on the dye orientation behavior in a lipid membrane with high spatiotemporal resolution representing a six-dimensional fluorescence detection approach.Entities:
Keywords: 3D dipole orientation; Anisotropy; Confocal microscopy; FCS; Fluorescence microscopy; GUV; Single molecule
Year: 2016 PMID: 26972111 DOI: 10.1007/s10895-016-1784-5
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217