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1.
Biophys J ; 104(7): 1456-64, 2013 Apr 02.
Artículo en Inglés | MEDLINE | ID: mdl-23561522

RESUMEN

We propose a novel, to our knowledge, method for the determination of tie lines in a phase diagram of ternary lipid mixtures. The method was applied to a system consisting of dioleoylphosphatidylcholine (DOPC), egg sphingomyelin (eSM), and cholesterol (Chol). The approach is based on electrofusion of single- or two-component homogeneous giant vesicles in the fluid phase and analyses of the domain areas of the fused vesicle. The electrofusion approach enables us to create three-component vesicles with precisely controlled composition, in contrast to conventional methods for giant vesicle formation. The tie lines determined in the two-liquid-phase coexistence region are found to be not parallel, suggesting that the dominant mechanism of lipid phase separation in this region changes with the membrane composition. We provide a phase diagram of the DOPC/eSM/Chol mixture and predict the location of the critical point. Finally, we evaluate the Gibbs free energy of transfer of individual lipid components from one phase to the other.


Asunto(s)
Colesterol/química , Óvulo/química , Fosfatidilcolinas/química , Esfingomielinas/química , Animales , Membrana Celular/química , Termodinámica
2.
Phys Rev Lett ; 108(12): 126102, 2012 Mar 23.
Artículo en Inglés | MEDLINE | ID: mdl-22540599

RESUMEN

Motivated by unexpected morphologies of the emerging liquid phase (channels, bulges, droplets) at the edge of thin, melting alkane terraces, we propose a new heterogeneous nucleation pathway. The competition between bulk and interfacial energies and the boundary conditions determine the growth and shape of the liquid phase at the edge of the solid alkane terraces. Calculations and experiments reveal a "precritical" shape transition (channel-to-bulges) of the liquid before reaching its critical volume along a putative shape-conserving path. Bulk liquid emerges from the new shape, and, depending on the degree of supersaturation, the new pathway may have two, one, or zero energy barriers. The findings are broadly relevant for many heterogeneous nucleation processes because the novel pathway is induced by common, widespread surface topologies (scratches, steps, etc.).

3.
Phys Rev E Stat Nonlin Soft Matter Phys ; 79(1 Pt 1): 011917, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19257079

RESUMEN

The velocity and the adenosine triphosphate (ATP) hydrolysis rate of the molecular motor kinesin are studied using a general network representation for the motor, which incorporates both the energetics of ATP hydrolysis and the experimentally observed separation of time scales between chemical and mechanical transitions. Both the motor velocity and its hydrolysis rate can be expressed as superpositions of excess fluxes for the directed cycles (or dicycles) of the network. The sign of these dicycle excess fluxes depends only on two thermodynamic control parameters as provided by the load force F and the chemical energy Deltamicro released during the hydrolysis of a single ATP molecule. In contrast, both the motor velocity and its hydrolysis rate depend, in general, on the load force F as well as on the three concentrations of ATP, adenosine diphosphate (ADP), and inorganic phosphate (P), separately. Thus, in order to represent the different operation modes of the motor in the (F,Deltamicro) plane, one has to specify two concentrations such as the product concentrations [ADP] and [P]. As a result, we find four different operation modes corresponding to the four possible combinations of ATP hydrolysis or synthesis with forward or backward mechanical steps. Our operation diagram implies in particular that backward steps are coupled to ATP hydrolysis for sufficiently large ATP concentrations, but to ATP synthesis for sufficiently large ADP and/or P concentrations.


Asunto(s)
Cinesinas/metabolismo , Adenosina Difosfato/metabolismo , Adenosina Trifosfato/metabolismo , Fenómenos Biomecánicos , Hidrólisis , Cinesinas/química , Cinética , Fosfatos/metabolismo , Probabilidad
4.
Curr Opin Struct Biol ; 5(4): 531-40, 1995 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-8528770

RESUMEN

Current research into the morphology of lipid membranes focuses on three areas: first, the transformations and fluctuations of the shape of freely suspended vesicles; second, the morphology of membranes that experience mutual interactions or external forces arising, for example, from a macroscopic surface or from optical tweezers; and third, the behavior of heterogeneous membranes with respect to bilayer asymmetry; intramembrane domains and anchored polymers. Our understanding of the morphology of lipid membranes has progressed substantially through the development of experimental techniques and theories.


Asunto(s)
Lípidos de la Membrana/química , Membrana Celular/química
5.
Soc Sci Med ; 34(6): 625-37, 1992 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-1574730

RESUMEN

A household interview survey combined with a serological survey on the incidence of malaria attacks and prevalence of antibodies has been carried out in rural and urban areas of the pacific coast of Colombia. Additional information on people's knowledge, attitudes and behaviour towards malaria was collected by means of participant observation and informal interviews. The results show that people incorporate modern and traditional elements into their concepts of the disease and treatment strategies. The deficiencies of the official control programmes are shown from the people's point of view. Some human factors which influence malaria transmission are discussed and an estimate of the accuracy of self-diagnosis presented.


Asunto(s)
Control de Enfermedades Transmisibles/métodos , Conocimientos, Actitudes y Práctica en Salud , Malaria/prevención & control , Autocuidado/métodos , Colombia/epidemiología , Humanos , Incidencia , Malaria/epidemiología , Malaria/inmunología , Prevalencia , Población Rural , Autocuidado/psicología , Estudios Seroepidemiológicos , Encuestas y Cuestionarios , Población Urbana
6.
Phys Rev E Stat Nonlin Soft Matter Phys ; 64(1 Pt 1): 011903, 2001 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-11461284

RESUMEN

Biomimetic membranes that contain several molecular components are studied theoretically. In contact with another surface, such as a solid substrate or another membrane, some of these intramembrane components are attracted by the second surface and, thus, act as local stickers. The cooperative behavior of these systems is characterized by the interplay of (i) attractive binding energies, (ii) entropic contributions arising from the shape fluctuations of the membranes, and (iii) the entropy of mixing of the stickers. A systematic study of this interplay, which starts from the corresponding partition functions, reveals that there are several distinct mechanisms for adhesion-induced phase separation within the membranes. The first of these mechanisms is effective for flexible stickers with attractive cis interactions (within the same membrane) and arises from the renormalization of these interactions by the confined membrane fluctuations. A second, purely entropic mechanism is found for rigid stickers without attractive cis interactions and arises from a fluctuation-induced line tension. Finally, a third mechanism is present if the membrane contains both stickers and repellers, i.e., nonadhesive molecules that protrude from the membrane surface. This third mechanism is based on an effective potential barrier and becomes less effective if the shape fluctuations of the membrane become more pronounced.


Asunto(s)
Biofisica/métodos , Adhesión Celular , Membrana Celular/química , Membranas Artificiales , Entropía , Membrana Dobles de Lípidos/química , Modelos Estadísticos , Método de Montecarlo , Temperatura
7.
Phys Rev Lett ; 57(22): 2876, 1986 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-10033895
8.
Phys Rev Lett ; 77(8): 1652-1655, 1996 Aug 19.
Artículo en Inglés | MEDLINE | ID: mdl-10063132
9.
Phys Rev Lett ; 55(16): 1699, 1985 Oct 14.
Artículo en Inglés | MEDLINE | ID: mdl-10031897
10.
Phys Rev Lett ; 62(7): 704-707, 1989 Feb 13.
Artículo en Inglés | MEDLINE | ID: mdl-10040311
11.
Phys Rev Lett ; 58(17): 1796, 1987 Apr 27.
Artículo en Inglés | MEDLINE | ID: mdl-10034538
12.
Phys Rev Lett ; 59(15): 1679-1682, 1987 Oct 12.
Artículo en Inglés | MEDLINE | ID: mdl-10035301
13.
Phys Rev Lett ; 60(23): 2394-2397, 1988 Jun 06.
Artículo en Inglés | MEDLINE | ID: mdl-10038340
14.
Phys Rev Lett ; 60(3): 242, 1988 Jan 18.
Artículo en Inglés | MEDLINE | ID: mdl-10038490
15.
Phys Rev Lett ; 61(21): 2508, 1988 Nov 21.
Artículo en Inglés | MEDLINE | ID: mdl-10039142
16.
Phys Rev Lett ; 56(23): 2541-2544, 1986 Jun 09.
Artículo en Inglés | MEDLINE | ID: mdl-10033019
17.
Phys Rev Lett ; 56(5): 472-475, 1986 Feb 03.
Artículo en Inglés | MEDLINE | ID: mdl-10033201
18.
Phys Rev Lett ; 57(19): 2411-2414, 1986 Nov 10.
Artículo en Inglés | MEDLINE | ID: mdl-10033718
19.
Phys Rev Lett ; 57(3): 353-356, 1986 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-10034038
20.
Phys Rev Lett ; 65(23): 2893-2896, 1990 Dec 03.
Artículo en Inglés | MEDLINE | ID: mdl-10042725
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