Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Angew Chem Int Ed Engl ; 57(45): 14932-14936, 2018 11 05.
Artículo en Inglés | MEDLINE | ID: mdl-30129689

RESUMEN

Membrane fusion is an essential process in nature and is often accomplished by the specific interaction of SNARE proteins. SNARE model systems, in which SNARE domains are replaced by small artificial units, represent valuable tools to study membrane fusion in vitro. The synthesis and analysis is presented of SNARE model peptides that exhibit a recognition motif composed of two different types of peptide nucleic acid (PNA) sequences. This novel recognition unit is designed to mimic the SNARE zippering mechanism that initiates SNARE-mediated fusion. It contains N-(2-aminoethyl)glycine-PNA (aeg-PNA) and alanyl-PNA, which both recognize the respective complementary strand but differ in duplex topology and duplex formation kinetics. The duplex formation of PNA hybrid oligomers as well as the fusogenicity of the model peptides in lipid-mixing assays were characterized and the peptides were found to induce liposome fusion. As an unexpected discovery, peptides with a recognition unit containing only five aeg-PNA nucleo amino acids were sufficient and most efficient to induce liposome fusion.


Asunto(s)
Liposomas/química , Ácidos Nucleicos de Péptidos/química , Péptidos/química , Proteínas SNARE/química , Dicroismo Circular , Liposomas/metabolismo , Fusión de Membrana , Modelos Moleculares , Ácidos Nucleicos de Péptidos/metabolismo , Péptidos/metabolismo , Proteínas SNARE/metabolismo
2.
FEBS Lett ; 592(6): 939-948, 2018 03.
Artículo en Inglés | MEDLINE | ID: mdl-29453892

RESUMEN

The HIV-1 envelope gp120/gp41 trimer mediates viral membrane fusion. After cluster of differentiation-4 recognition, gp120 detaches from the virus, exposing gp41 which triggers fusion. During the fusion process, gp41 may not remain trimeric, which could have functional importance. Here, we probe the reversible association of full length gp41 (minus the cytoplasmic domain) in detergent micelles (with probes attached to transmembrane domain) by fluorescence resonance energy transfer (FRET) with a µm dissociation constant. This is compared with other methods. A gp41-targeted fusion inhibitor must interfere with this transition, and monomeric, partially monomeric or trimeric states all present potential binding epitopes. The gp41 self-association is a valid drug target model and FRET, a potential high-throughput assay system, could be used to screen drug libraries.


Asunto(s)
Proteína gp41 de Envoltorio del VIH/química , VIH-1/química , Multimerización de Proteína , Transferencia Resonante de Energía de Fluorescencia , Proteína gp41 de Envoltorio del VIH/genética , Proteína gp41 de Envoltorio del VIH/metabolismo , VIH-1/genética , VIH-1/metabolismo , Micelas
4.
PLoS One ; 10(5): e0128241, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26020927

RESUMEN

Two-photon fluorescence correlation spectroscopy (2P-FCS) within single dendritic spines of living hippocampal pyramidal neurons was used to resolve various subpopulations of mobile F-actin during activity-dependent structural changes such as potentiation induced spine head growth. Two major classes of mobile F-actin were discovered: very dynamic and about a hundred times less dynamic F-actin. Spine head enlargement upon application of Tetraethylammonium (TEA), a protocol previously used for the chemical induction of long-term potentiation (cLTP) strictly correlated to changes in the dynamics and filament numbers in the different actin filament fractions. Our observations suggest that spine enlargement is governed by a mechanism in which longer filaments are first cut into smaller filaments that cooperate with the second, increasingly dynamic shorter actin filament population to quickly reorganize and expand the actin cytoskeleton within the spine head. This process would allow a fast and efficient spine head enlargement using a major fraction of the actin filament population that was already present before spine head growth.


Asunto(s)
Citoesqueleto de Actina/ultraestructura , Actinas/química , Región CA3 Hipocampal/ultraestructura , Espinas Dendríticas/ultraestructura , Citoesqueleto de Actina/genética , Citoesqueleto de Actina/metabolismo , Actinas/clasificación , Actinas/genética , Actinas/metabolismo , Animales , Animales Recién Nacidos , Región CA3 Hipocampal/efectos de los fármacos , Región CA3 Hipocampal/metabolismo , Espinas Dendríticas/efectos de los fármacos , Espinas Dendríticas/genética , Espinas Dendríticas/metabolismo , Expresión Génica , Potenciación a Largo Plazo/fisiología , Ratones , Ratones Endogámicos C57BL , Cultivo Primario de Células , Espectrometría de Fluorescencia/métodos , Tetraetilamonio/farmacología
5.
Nat Methods ; 11(5): 579-84, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24705472

RESUMEN

When excited with rotating linear polarized light, differently oriented fluorescent dyes emit periodic signals peaking at different times. We show that measurement of the average orientation of fluorescent dyes attached to rigid sample structures mapped to regularly defined (50 nm)(2) image nanoareas can provide subdiffraction resolution (super resolution by polarization demodulation, SPoD). Because the polarization angle range for effective excitation of an oriented molecule is rather broad and unspecific, we narrowed this range by simultaneous irradiation with a second, de-excitation, beam possessing a polarization perpendicular to the excitation beam (excitation polarization angle narrowing, ExPAN). This shortened the periodic emission flashes, allowing better discrimination between molecules or nanoareas. Our method requires neither the generation of nanometric interference structures nor the use of switchable or blinking fluorescent probes. We applied the method to standard wide-field microscopy with camera detection and to two-photon scanning microscopy, imaging the fine structural details of neuronal spines.


Asunto(s)
Polarización de Fluorescencia/métodos , Microscopía Fluorescente/métodos , Nanotecnología/métodos , Algoritmos , Animales , Células Cultivadas , Simulación por Computador , Células Epiteliales/metabolismo , Diseño de Equipo , Colorantes Fluorescentes/química , Proteínas Fluorescentes Verdes/metabolismo , Microtúbulos/ultraestructura , Modelos Teóricos , Nanosferas/química , Distribución Normal , Fotones , Potoroidae , Programas Informáticos
6.
Proc Natl Acad Sci U S A ; 110(14): 5452-6, 2013 Apr 02.
Artículo en Inglés | MEDLINE | ID: mdl-23509270

RESUMEN

The photosystem II (PSII) subunit S (PsbS) plays a key role in nonphotochemical quenching, a photoprotective mechanism for dissipation of excess excitation energy in plants. The precise function of PsbS in nonphotochemical quenching is unknown. By reconstituting PsbS together with the major light-harvesting complex of PSII (LHC-II) and the xanthophyll zeaxanthin (Zea) into proteoliposomes, we have tested the individual contributions of PSII complexes and Zea to chlorophyll (Chl) fluorescence quenching in a membrane environment. We demonstrate that PsbS is stable in the absence of pigments in vitro. Significant Chl fluorescence quenching of reconstituted LHC-II was observed in the presence of PsbS and Zea, although neither Zea nor PsbS alone was sufficient to induce the same quenching. Coreconstitution with PsbS resulted in the formation of LHC-II/PsbS heterodimers, indicating their direct interaction in the lipid bilayer. Two-photon excitation measurements on liposomes containing LHC-II, PsbS, and Zea showed an increase of electronic interactions between carotenoid S1 and Chl states, Φ(Coupling)(CarS1-Chl), that correlated directly with Chl fluorescence quenching. These findings are in agreement with a carotenoid-dependent Chl fluorescence quenching by direct interactions of LHCs of PSII with PsbS monomers.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Clorofila/metabolismo , Complejos de Proteína Captadores de Luz/metabolismo , Complejo de Proteína del Fotosistema II/metabolismo , Proteínas Recombinantes/metabolismo , Xantófilas/metabolismo , Arabidopsis , Western Blotting , Cromatografía Líquida de Alta Presión , Dicroismo Circular , Clonación Molecular , Electroforesis en Gel de Poliacrilamida , Liposomas/metabolismo , Pisum sativum , Pliegue de Proteína , Espectrometría de Fluorescencia , Zeaxantinas
7.
Proc Natl Acad Sci U S A ; 109(27): 11037-42, 2012 Jul 03.
Artículo en Inglés | MEDLINE | ID: mdl-22711810

RESUMEN

In neurotransmission synaptotagmin-1 tethers synaptic vesicles to the presynaptic plasma membrane by binding to acidic membrane lipids and SNAREs and promotes rapid SNARE-mediated fusion upon Ca(2+) triggering. However, recent studies suggested that upon membrane contact synaptotagmin may not only bind in trans to the target membrane but also in cis to its own membrane. Using a sensitive membrane tethering assay we have now dissected the structural requirements and concentration ranges for Ca(2+)-dependent and -independent cis-binding and trans-tethering in the presence and absence of acidic phospholipids and SNAREs. Using variants of membrane-anchored synaptotagmin in which the Ca(2+)-binding sites in the C2 domains and a basic cluster involved in membrane binding were disrupted we show that Ca(2+)-dependent cis-binding prevents trans-interactions if the cis-membrane contains 12-20% anionic phospholipids. Similarly, no trans-interactions were observable using soluble C2AB-domain fragments at comparable concentrations. At saturating concentrations, however, tethering was observed with soluble C2AB domains, probably due to crowding on the vesicle surface and competition for binding sites. We conclude that trans-interactions of synaptotagmin considered to be essential for its function are controlled by a delicate balance between cis- and trans-binding, which may play an important modulatory role in synaptic transmission.


Asunto(s)
Terminales Presinápticos/metabolismo , Transmisión Sináptica/fisiología , Vesículas Sinápticas/metabolismo , Sinaptotagmina I/química , Sinaptotagmina I/metabolismo , Animales , Sitios de Unión/fisiología , Calcio/metabolismo , Membrana Celular/metabolismo , Liposomas/metabolismo , Unión Proteica/fisiología , Estructura Terciaria de Proteína/fisiología , Ratas , Proteínas SNARE/metabolismo , Espectrometría de Fluorescencia , Sinaptotagmina I/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA