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1.
Eur Biophys J ; 39(8): 1277-80, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19937014

RESUMEN

Proteo-giant liposomes were electroformed from a mixture of lecithin vesicles and inside-out vesicles from erythrocytes. After addition of Mg-ATP in the vicinity of the proteo-giant liposomes, small buds appeared on the liposome surfaces, which--via an increase in lipids in the outer monolayer--demonstrated the active transport of lipids from the inner to the outer monolayer, indicating flippase activity.


Asunto(s)
Eritrocitos/enzimología , Eritrocitos/metabolismo , Lecitinas/metabolismo , Liposomas Unilamelares/metabolismo , Adenosina Trifosfato/metabolismo , Fluorescencia , Magnesio/metabolismo , Microscopía Fluorescente , Sodio/metabolismo , Estrés Mecánico , Tensión Superficial
2.
Biophys J ; 91(4): 1357-67, 2006 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-16731559

RESUMEN

Most studies reported until now on the magnetically alignable system formed by the binary mixtures of long- and short-chain lipids were based on the mixture of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (D14PC) and 1,2-dihexanoyl-sn-glycero-3-phosphocholine (D6PC) lipids. We have recently shown that a large part of the phase diagrams of this lipid mixture could be understood by taking into account the partial miscibility between the long-chain lipids and the short-chain lipids when the sample was heated above the melting transition temperature (Tm) of the long-chain lipids. In this work, we show by modifying the chain length of either one of the two lipids that it is possible to control their miscibility and thus the intervals of temperature and composition where spontaneous alignment is observed in a magnetic field. By using 31P NMR, we demonstrate that the very special properties of such binary lipid mixtures are correlated with the propensity for short-chain lipids to diffuse into the bilayer regions. We also show that lipid mixtures with comparable properties can be formed with unsaturated lipids such as 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC).


Asunto(s)
Coloides/química , Grasas Insaturadas/química , Membrana Dobles de Lípidos/química , Fosfatidilcolinas/química , Coloides/análisis , Grasas Insaturadas/análisis , Membrana Dobles de Lípidos/análisis , Espectroscopía de Resonancia Magnética , Micelas , Peso Molecular , Transición de Fase , Fosfatidilcolinas/análisis , Fósforo , Solubilidad , Relación Estructura-Actividad , Temperatura
3.
Biophys J ; 88(3): 1887-901, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15626702

RESUMEN

Mixtures of dimyristoyl-phosphatidylcholine (DMPC) and dihexanoyl-phosphatidylcholine (DHPC) in water form disks also called bicelles and different bilayer organizations when the mol ratio of the two lipids and the temperature are varied. The spontaneous alignment in a magnetic field of these bilayers above the transition temperature T(m) of DMPC is an attractive property that was successfully used to investigate protein structure by NMR. In this article, we have attempted to give an overview of all structural transformations of DMPC/DHPC mixtures that can be inferred from broad band (31)P-NMR spectroscopy between 5 and 60 degrees C. We show that above a critical temperature, T(v), perforated vesicles progressively replace alignable structures. The holes in these vesicles disappear above a new temperature threshold, T(h). The driving force for these temperature-dependent transformations that has been overlooked in previous studies is the increase of DHPC miscibility in the bilayer domain above T(m). Accordingly, we propose a new model (the "mixed bicelle" model) that emphasizes the consequence of the mixing. This investigation shows that the various structures of DMPC in the presence of increasing mol ratios of the short-chain DHPC is reminiscent of the observation put forward by several laboratories investigating solubilization and reconstitution of biological membranes.


Asunto(s)
Dimiristoilfosfatidilcolina/química , Membrana Dobles de Lípidos/química , Liposomas/química , Espectroscopía de Resonancia Magnética/métodos , Fluidez de la Membrana , Modelos Químicos , Éteres Fosfolípidos/química , Coloides/análisis , Coloides/química , Simulación por Computador , Dimiristoilfosfatidilcolina/análisis , Membrana Dobles de Lípidos/análisis , Liposomas/análisis , Micelas , Conformación Molecular , Transición de Fase , Éteres Fosfolípidos/análisis , Fósforo , Solubilidad , Temperatura , Agua/química
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