S. Milles, T. Meyer, H.A. Scheidt, R. Schwarzer, L. Thomas, M. Marek, L. Szente, R. Bittman, A. Herrmann, T. Günther Pomorski, D. Huster, and P. Müller (2013).
Organization of fluorescent cholesterol analogs in lipid bilayers – Lessons from cyclodextrin extraction.
Biochimica et Biophysica Acta – Biomembranes 1828(8): 1822–1828.
doi: 10.1016/j.bbamem.2013.04.002
To characterize the structure and dynamics of cholesterol in membranes, fluorescent analogs of the native molecule have widely been employed. The cholesterol content in membranes is in general manipulated by using water-soluble cyclodextrins. Since the interactions between cyclodextrins and fluorescent-labeled cholesterol have not been investigated in detail so far, we have compared the cyclodextrin-mediated membrane extraction of three different fluorescent cholesterol analogs (one bearing a NBD and two bearing BODIPY moieties). Extraction of these analogs was followed by measuring the Förster resonance energy transfer between a rhodamine moiety linked to phosphatidylethanolamine and the labeled cholesterol. The extraction kinetics revealed that the analogs are differently extracted from membranes. We examined the orientation of the analogs within the membrane and their influence on lipid condensation using NMR and EPR spectroscopies. Our data indicate that the extraction of fluorescent sterols from membranes is determined by several parameters, including their impact on lipid order, their hydrophobicity, their intermolecular interactions with surrounding lipids, their orientation within the bilayer, and their affinity with the exogenous acceptor.