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Título

Liquid-crystalline, liquid-ordered, rippled and gel lipid bilayer phases as observed with nile red fluorescence

AutorSot, Jesús CSIC ORCID; Gartzia-Rivero, Leire; Bañuelos, Jorge; Goñi, Félix M. CSIC ORCID; Alonso, Alicia CSIC ORCID
Palabras claveLipid bilayer phases
Nile red
Phospholipid rippled phases
FLIM
Fluorescence
Fecha de publicación1-oct-2022
EditorElsevier BV
CitaciónJournal of Molecular Liquids 363: 119874 (2022)
ResumenThe basic matrix of cellular membranes consists of a double layer (bilayer) of phospholipids. Semisynthetic lipid bilayers are commonly used in biophysical studies of membranes. According to temperature and composition, lipid bilayers can exist in liquid-crystalline (or liquid-disordered), liquid-ordered, rippled, and gel phases. In the present study, the hydrophobic, solvatochromic molecule Nile red has been used as a fluorescent probe to examine the physical state of bilayers of different compositions in the 15–60 °C range. Phospholipids with saturated or unsaturated acyl chains, in the presence or absence of cholesterol have been studied. Nile red shows absorption maxima at 520–550 nm and emission maxima at 580–640 nm, single photon excitation not being damaging to the system. A red/orange intensity ratio (ROIR) index has been used to normalize the results. ROIR varies clearly and reproducibly with the lipid phase, increasing in the order: liquid-ordered < gel < rippled < liquid-crystalline. It increases with temperature and decreases with cholesterol contents in the bilayers. Nile red allows an unusually clear observation of the rippled-to-liquid crystalline phase transition in saturated phospholipids. FLIM studies with Nile red also show differences between lamellar phases. Rotational relaxation times have been determined for Nile red in liquid-disordered (0.72 ± 0.010 ns), gel (1.16 ± 0.070 ns), and liquid-ordered (1.79 ± 0.14 ns) phases, the large value of the liquid-ordered phase being an indication of the sterol hindering probe tumbling in the hydrophobic matrix.
Versión del editorhttps://doi.org/10.1016/j.molliq.2022.119874
URIhttp://hdl.handle.net/10261/296429
DOI10.1016/j.molliq.2022.119874
ISSN0167-7322
E-ISSN1873-3166
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