Literatura académica sobre el tema "Interaction supramoléculaire"
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Artículos de revistas sobre el tema "Interaction supramoléculaire"
Sakho, Adama Moussa, Aboubacar Diallo, Kaba Conde, Damany Keita, Mamady Kourouma, Dong Sheng Zhu y Bangaly Dioumessy. "Synthèse, caractérisation et l’activité anti-tumorale d’un complexe organo-étain carboxylique". International Journal of Biological and Chemical Sciences 14, n.º 3 (19 de junio de 2020): 1133–43. http://dx.doi.org/10.4314/ijbcs.v14i3.38.
Texto completoFAVERDIN, P. y C. LEROUX. "Avant-propos". INRAE Productions Animales 26, n.º 2 (16 de abril de 2013): 71–76. http://dx.doi.org/10.20870/productions-animales.2013.26.2.3137.
Texto completoTesis sobre el tema "Interaction supramoléculaire"
Chevalier, Sébastien. "Etude de l'assemblage supramoléculaire des cadhérines, et dynamique d'adhésion". Phd thesis, Université Sciences et Technologies - Bordeaux I, 2009. http://tel.archives-ouvertes.fr/tel-00752404.
Texto completoWilczewski, Marie. "Les interactions multivalentes : leurs rôles dans les processus de reconnaissance biomoléculaire et leur application dans la construction d'assemblage supramoléculaire". Phd thesis, Université Joseph Fourier (Grenoble), 2007. http://tel.archives-ouvertes.fr/tel-00196867.
Texto completoDeux chapitres sont axés sur l'utilisation de plateformes supramoléculaires cyclodécapeptidiques appelées RAFT (Regioselectively Adressable Functionnalized Template) permettant la présentation multiple de ligand saccharidique ou cyclopeptidique. Une étude cinétique et thermodynamique des interactions entre les ligands RAFT-saccharide et une lectine modèle, la concanavaline A, a permis de démontrer que deux mécanismes moléculaires sont à l'origine de la meilleure affinité des RAFT multivalents par rapport à leurs homologues monovalents : d'une part un effet de « proximité-statistique » dû à la concentration locale élevée en motif sucre et d'autre part la capacité des RAFT multivalents à se lier à plusieurs lectines selon un effet « cluster ». Des études préliminaires ont également concerné l'analyse de l'interaction entre RAFT-RGD et des récepteurs cellulaires.
Dans un dernier chapitre, nous avons démontré, pour la première fois, la formation de films multicouches grâce à des interactions de type hôte-invité entre deux biopolymères de chitosane, l'un fonctionnalisés par des cavités Β-cyclodextrine et l'autre par des entités adamantane. Bien que la stabilité de l'assemblage soit assurée par des interactions de complexation multivalentes, la croissance de l'assemblage, quant à elle, dépend de la disponibilité des sites de complexation offerts par chacune des couches. De plus, les deux polymères chargés positivement confèrent à l'assemblage des propriétés de gonflement-dégonflement en réponse à des variations de force ionique et pH.
Wilczewski, Marie. "Les interactions multivalentes : leurs rôles dans les processus de reconnaissance biomoléculaire et leur application dans la construction d'assemblage supramoléculaire". Phd thesis, Grenoble 1, 2007. http://www.theses.fr/2007GRE10253.
Texto completoThis work deals with a quantitative study of several biomolecular recognition systems involving multivalent interactions. Two chapters focuse on the use of supramolecular cyclodecapeptidic platform called RAFT (Regioselectively Addressable Functionnalized Template), which allows the presentation of multiple carbohydrate or cyclopeptidic ligands. Kinetic and thermodynamic studies of the interaction between the ligands RAFT-carbohydrate and a model lectin, concanavalin A, have demonstrated that two molecular mechanisms are responsible for the better affinity of multivalent RAFT molecule compared to their monovalent counterparts: on one hand a "proximity-statistical" effect due to the high local concentration of sugar entities and on the other hand thanks to a "cluster effect" which confers the ability of multivalent RAFT to bind several lectins. Preliminary studies have also involved the analysis of the interaction between RAFT-RGD and integrin cell receptors. In a last chapter, we have demonstrated, for the first time, polymer multilayer formation based on host-guest interaction between two derivatized chitosans biopolymers, one, with -cyclodextrin cavities and the other with adamantyl moieties. While stability of the self-assembly is conferred by multivalent complexation occuring at each step of the construction, the assembly growth is mainly governed by the availability of the complexation sites offered by each layer. Moreover, the two positively charged polymers confer to the assembly swelling/deswelling properties in response to changes in ionic strength and pH
Chevalier, Sébastien. "Etude de l’assemblage supramoléculaire des cadhérines et dynamique d’adhésion". Thesis, Bordeaux 1, 2009. http://www.theses.fr/2009BOR13970/document.
Texto completoCell adhesion receptors of the classical cadherin family are involved in Ca2+-dependent homophilic interactions. In order to dissect the molecular mechanisms of cadherin-based cellcell adhesion, this Ph.D. thesis describes a comparative dynamic study of interactions between cadherins E- & -11, chosen as classical type I and II cadherins prototypes respectively. Modifications of particular residues in the E-cadherin adhesive interface showed that the ?-strand exchange with its Trp2 had a prominent feature; for type II cadherins, a different mechanism was described involving a larger domain swapping. We then developed a new protocol for immobilizing proteins in an orientated and covalent manner on surfaces. These interactions regulate signalization pathways in various biological processes. Studies describing Stat3 activation through direct cadherin engagement are reviewed
Mimassi, Lamia. "Auto-assemblage raisonné de métallo-macrocycles et de polymères de coordination : chiralité, reconnaissance et encapsulation d'ions". Paris 6, 2005. http://www.theses.fr/2005PA066157.
Texto completoJaquillard, Lucie. "Spectrométrie de masse supramoléculaire : caractérisation de l'intéraction non-covalente entre PEBP1/RKIP humaine et des analogues de nucléotides". Phd thesis, Université d'Orléans, 2012. http://tel.archives-ouvertes.fr/tel-00923153.
Texto completoGenest, Aymeric. "Application de la réaction aza-Michael à l'élaboration de matériaux silicones supramoléculaires". Thesis, Lyon, INSA, 2015. http://www.theses.fr/2015ISAL0129.
Texto completoThis PhD thesis was focused on the incorporation of functional groups onto the siloxane polymer backbone such that supramolecular assemblies are formed, in order to prepare new supramolecular silicone materials. First, an in-depth review of the aza-Michael reaction applied to silicon-containing compounds was realized, highlighting the whole potential of this addition reaction. The aza-Michael reaction applied to organic amines was thoroughly analyzed in order to emphasize some open issues such as selectivity or retro-aza-Michael reaction. In order to understand and master the aza-Michael reaction, a model reaction involving a bis-(3-aminopropyl)-terminated PDMS and butylacrylate was then fully investigated. Operating parameters such as protic polar solvents, catalysts or temperature allow promoting the reaction rate. Kinetic data showed that the selectivity towards the main formation of mono- or di-adduct can be controlled by carefully selecting the solvent nature and content. The syntheses of 100% mono- and 100% di-adduct compounds was succesfully achieved. The aza-Michael reaction was then applied to a less reactive Michael acceptor, i.e. acrylic acid. This unsaturated organic acid reacts instantaneously with amines by acid-base reaction leading to the formation of ionic pairs. This acid-base equilibrium is then shifted in the forward direction allowing the synthesis of zwitterionic groups by aza-Michael. The aza-Michael reaction of this peculiar Michael acceptor was thoroughly investigated both with simple organic amines and aminosilicone oligomers and polymers in order to elucidate the structures and to evaluate the rheological properties. Finally, supramolecular silicone materials bearing zwitterionic-like groups were prepared leading to supramolecular materials with properties ranging from visco-elastic liquids to thermoplastic silicone elastomers
Becard, Stéphanie. "Développements méthodologiques en spectrométrie de masse et en mobilité ionique pour l'étude d'assemblages supramoléculaires en biologie". Phd thesis, Université de Strasbourg, 2012. http://tel.archives-ouvertes.fr/tel-00832488.
Texto completoBécard, Stéphanie. "Développements méthodologiques en spectrométrie de masse et en mobilité ionique pour l'étude d'assemblages supramoléculaires en biologie". Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAF036/document.
Texto completoThe aim of this thesis was the development of different supramolecular approaches, like MS and IM-MS, to characterize precisely protein/ligand interaction and to analyze complex mixtures of proteins. Understanding of supramolecular MS instruments and instrumental and methodological optimizations were allowed the development of MS and IM-MS to characterize very high mass supramolecular assembly. Thus, we were able to follow by kinetic the formation of protein/ligand interaction as well as associated conformational modifications, showing the interest of IM-MS coupling in pharmaceutical research. Furthermore, this work deals with the study of high mass complexes and assessment of IM-MS to obtain structural information on these complexes. As a consequence, we have pushed away some limits of MS allowing the use of this technique in structural biology
Trabolsi, Ali. "Etudes des interactions dans des édifices supramoléculaires". Université Louis Pasteur (Strasbourg) (1971-2008), 2006. http://www.theses.fr/2006STR13210.
Texto completoThe research data presented in this PhD dissertation contribute to a better understanding of the ionic and molecular recognition mechanisms, which are involved in the self-assembly of novel photochemical supramolecules. We first have focused our attention on strapped Zn(II) porphyrinic receptors which possess a fine-tuned and appropriate architecture for the strong and selective recognition of imidazole substrates. The flexibility of these receptors associated to a set of strong (Zn-N coordination bond) and weak (hydrogen bond, - and CH- interactions) intramolecular interactions are responsible of the specificity and efficiency of the binding processes. The efficiency of the recognition processes is adjusted and controlled by the nature and bulkiness of the substituents. Our physico-chemical approach thus helped to guide the synthesis toward new imidazole-porphyrin substrates and was an essential stage toward the development of stable photochemical devices for which the photoinduced energy migration processes are very efficient. We also explored the possibility to pair C60 and polyphenylnevinylene oligomers or metalloporphyrins using a supramolecular approach. Axial coordination of nitrogen bases on Zn(II) porphyrins and ionic recognition of ammoniums by 18C6 crown-ethers were chosen as primary interactions. To strengthen these edifices, assembly strategies with polytopic receptors were processed and successfully led to the formation of stable edifices. The photoinduced processes within these new supramolecules were studied. The first strategy relies on positively cooperative association of two substrates, which mainly results from secondary - interactions between two C60 units positioned in a syn conformation. The second strategy uses multivalent supramolecular chemistry and is based on the macrocyclization process of bivalent substrates with ditopic receptors
Libros sobre el tema "Interaction supramoléculaire"
Aseyev, Georgii Georgievich. Electrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Buscar texto completoAseyev, Georgii Georgievich. Electrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Buscar texto completoElectrolytes: Supramolecular Interactions and Non-Equilibrium Phenomena in Concentrated Solutions. Taylor & Francis Group, 2014.
Buscar texto completoCapítulos de libros sobre el tema "Interaction supramoléculaire"
"18. Y a-t-il une interaction de reconnaissance entre les oligosaccharides et l’ADN ?" En Chimie moléculaire et supramoléculaire des sucres, 280–92. EDP Sciences, 1995. http://dx.doi.org/10.1051/978-2-7598-0267-8.c019.
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