Literatura académica sobre el tema "Synthetic Self-assembling Amino Acid"
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Artículos de revistas sobre el tema "Synthetic Self-assembling Amino Acid"
Lesiak, Marta, Aleksandra Augusciak-Duma, Anna Szydlo, Ksymena Pruszczynska y Aleksander L. Sieron. "Specific inhibition of procollagen C-endopeptidase activity by synthetic peptide with conservative sequence found in chordin." Acta Biochimica Polonica 55, n.º 2 (7 de junio de 2008): 297–305. http://dx.doi.org/10.18388/abp.2008_3076.
Texto completoGaynanova, Gulnara, Leysan Vasileva, Ruslan Kashapov, Darya Kuznetsova, Rushana Kushnazarova, Anna Tyryshkina, Elmira Vasilieva, Konstantin Petrov, Lucia Zakharova y Oleg Sinyashin. "Self-Assembling Drug Formulations with Tunable Permeability and Biodegradability". Molecules 26, n.º 22 (10 de noviembre de 2021): 6786. http://dx.doi.org/10.3390/molecules26226786.
Texto completoTinajero-Díaz, E., A. Martínez de Ilarduya, B. Cavanagh, A. Heise y S. Muñoz-Guerra. "Poly(amino acid)-grafted polymacrolactones. Synthesis, self-assembling and ionic coupling properties". Reactive and Functional Polymers 143 (octubre de 2019): 104316. http://dx.doi.org/10.1016/j.reactfunctpolym.2019.104316.
Texto completoLiu, Renjie y Gregory A. Hudalla. "Using Self-Assembling Peptides to Integrate Biomolecules into Functional Supramolecular Biomaterials". Molecules 24, n.º 8 (12 de abril de 2019): 1450. http://dx.doi.org/10.3390/molecules24081450.
Texto completoRosselin, Marie, Grégory Meyer, Pierre Guillet, Thomas Cheviet, Guillaume Walther, Annette Meister, Dimitra Hadjipavlou-Litina y Grégory Durand. "Divalent Amino-Acid-Based Amphiphilic Antioxidants: Synthesis, Self-Assembling Properties, and Biological Evaluation". Bioconjugate Chemistry 27, n.º 3 (22 de febrero de 2016): 772–81. http://dx.doi.org/10.1021/acs.bioconjchem.6b00002.
Texto completoZhang, Shuguang. "Discovery and design of self-assembling peptides". Interface Focus 7, n.º 6 (20 de octubre de 2017): 20170028. http://dx.doi.org/10.1098/rsfs.2017.0028.
Texto completoDutta, Arpita, Suven Das, Purak Das, Suvendu Maity, Prasanta Ghosh y Soumya Shankha Biswas. "Unique supramolecular assembly of a synthetic achiral α, γ-hybrid tripeptide". Zeitschrift für Kristallographie - Crystalline Materials 237, n.º 1-3 (1 de marzo de 2022): 77–81. http://dx.doi.org/10.1515/zkri-2022-0002.
Texto completoMachado, Raul, A. J. Ribeiro, J. Padrão, D. Silva, A. Nobre, J. A. Teixeira, F. J. Arias, António M. Cunha, José C. Rodríguez-Cabello y M. Casal. "Exploiting the Sequence of Naturally Occurring Elastin: Construction, Production and Characterization of a Recombinant Thermoplastic Protein-Based Polymer". Journal of Nano Research 6 (junio de 2009): 133–45. http://dx.doi.org/10.4028/www.scientific.net/jnanor.6.133.
Texto completoDas, Apurba K., Swarup Manna, Michael G. B. Drew, Sudip Malik, Arun K. Nandi y Arindam Banerjee. "Low Molecular Weight Organogelators from Self-assembling Synthetic Tripeptides With Coded Amino Acids: Morphological, Structural, Thermodynamic and Spectroscopic Investigations". Supramolecular Chemistry 18, n.º 8 (1 de diciembre de 2006): 645–55. http://dx.doi.org/10.1080/10610270601035553.
Texto completoVarlas, Spyridon, Georgia L. Maitland y Matthew J. Derry. "Protein-, (Poly)peptide-, and Amino Acid-Based Nanostructures Prepared via Polymerization-Induced Self-Assembly". Polymers 13, n.º 16 (5 de agosto de 2021): 2603. http://dx.doi.org/10.3390/polym13162603.
Texto completoTesis sobre el tema "Synthetic Self-assembling Amino Acid"
LOCARNO, SILVIA ALICE. "UNNATURAL AMINO ACIDS AS SYNTHETIC TOOLS FOR THE PREPARATION OF COMPLEX MOLECULAR ARCHITECTURES". Doctoral thesis, Università degli Studi di Milano, 2019. http://hdl.handle.net/2434/607175.
Texto completoKonstantopoulos, Antonios. "Self-assembling octapeptides : effect of amino acid size and charge distribution". Thesis, University of Manchester, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492888.
Texto completoSmith, Mark T. "Engineering Cell-Free Systems for Vaccine Development, Self-Assembling Nanoparticles and Codon Reassignment Applications". BYU ScholarsArchive, 2014. https://scholarsarchive.byu.edu/etd/4449.
Texto completoSadowski, John Paul. "Design and synthesis of dynamically assembling DNA nanostructures". Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:11272.
Texto completoChemistry and Chemical Biology
Ménard, Nathalie. "Tensioactifs d’origine naturelle pour la solubilisation de principes actifs : synthèse, physico-chimie et toxicité". Thesis, Paris 11, 2011. http://www.theses.fr/2011PA114832/document.
Texto completoThe aim of this thesis was to develop novel surfactants, able to self-assemble into micelles and to solubilize insoluble drugs intented for intravenous injection. Natural-based surfactants were synthesized and their physico-chemical properties were evaluated. In addition, their in vitro and in vivo toxicity were evaluated. Their drug solubilization abitity was also investigated. Three surfactant classes were evaluated. They were composed of a hydrophobic moiety, such as cholesterol, bile salts or lipids, bonded to a hydrophilic moiety, deriving from amino acids, such as lysine, glutamine or glutamic acid, via an amide bond.The influence of surfactant hydrophobic moiety flexibility on drug solubilization ability was evaluated. This study evidenced that solubilization efficiency is related to the surfactant hydrophobic moiety flexibility. The use of surfactants with flexible and saturated lipidic moieties increased drug water solubility with a drug loading of 46 % (w/w). Saturated lipid-based surfactants exhibited a better solubilization efficiency, in comparison with steroid-based surfactants or poly-unsaturated-based surfactants. Toxicity studies evidenced the relation between surfactant chemical structure and their toxicity, in particular with cell membranes. The introduction of double bond in cis configuration in surfactant lipidic moiety decreased their interaction with cell membranes and thus their toxicity. In addition, this chemical modification also decreased their solubilization ability. To develop novel surfactants, it is thus necessary to take into account drug solubilization ability and toxicity of surfactants
Awada, Hawraà. "Synthèse sélective de γ-amino acides cyclobutaniques : préparation de nouveaux organogélateurs peptidiques". Thesis, Paris 11, 2014. http://www.theses.fr/2014PA112365/document.
Texto completoThe γ-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the central nervous system (CNS). In order to obtain new enantiomerically pure cyclobutanic derivative of GABA, the cis-3,4CB-GABA, two efficient synthetic strategies have been established. Both synthetic routes employed a photocycloaddition [2 +2] protocol, which provided the cyclobutanic ring. The first route involved the homolgation of the cis-2-aminocyclobutanecarboxylic acid (cis-ACBC), whereas the second route is a multi-step synthesis using caprolactam as starting material.On the other hand, the (1R,2S)-cis-GABA-2,3CB was synthetized, and a series of N- and C-protected oligomers of di, tri, and tetrapeptides of this amino acid were prepared. These oligomers were characterized by NMR (1D and 2D) techniques, IR, and X-ray. The analyses have shown that there are no non-covalent interactions (hydrogen bonds) between the residues of each oligomers. However, the gelation property of these oligomers in various organic solvents was demonstrated. Solutions and gels formed from these peptides were analyzed by scanning electron microscopy, and the obtained images showed a fibrous organization of the di- and tetrapeptide, while the tripeptide showed no regular intermolecular assembly
Rapisarda, Alessandro. "Novel self-assembled monolayer (SAM) based on calix[n]arenes for application as chemical sensors and optical devices: synthesis, studies and applications". Doctoral thesis, Università di Catania, 2013. http://hdl.handle.net/10761/1281.
Texto completoHu, Xiaobo. "Synthèse, analyses structurales et assemblage de foldamères oligoamide hydrosolubles à base de quinolines". Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0611/document.
Texto completoFoldamer chemistry is a rapidly expanding research field where chemists explore the construction of various artificial architectures that mimic the folded structures of biopolymers found in nature. Quinoline oligoamide foldamers, as an important branch of foldamers, have been shown to possess many desirable features, including stability and predictability of their folded conformations, and are promising candidates to achieve biological applications. Up to now, most investigations of quinoline oligoamide foldamers have been carried out in organic solvents. This thesis is aimed to expand their scope in aqueous medium and presents several methodologies to achieve solubility, folding, side-chain variation, aggregation and crystal growth ability in water.First, a solid phase synthesis method was developed to enable the fast access to α-amino acid/quinoline (X/Q) hybrid oligoamide foldamers. The study of these hybrid foldamers in water showed that contrary to (XQ)n-type foldamers the (XQ2)n-type foldamers could adopt aromatic helical conformations with α-amino acid side chains aligned in space. Then, several short side chains were identified to endow aromatic foldamers with both solubility in, and crystal growth ability from water. Six quinoline oligoamides displaying these side chains were synthesized as a case study. Crystals were obtained from aqueous medium in all cases but one, exceedingly soluble in water. At last, efforts were made to construct self-assembled aromatic helix bundles in water based on hydrophobic effects and electrostatic interactions. NMR and crystallographic studies indicated that hydrophobic effects are weaker than expected and not strongly conducive of aggregation
Rost, Ulrike. "Organisation and Recognition of Artificial Transmembrane Peptides". Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-002B-7CA6-D.
Texto completo"A library of natural alpha-amino acid-based dendrons synthesis, characterization and self-assembling properties". 2003. http://library.cuhk.edu.hk/record=b6073532.
Texto completoThesis (Ph.D.)--Chinese University of Hong Kong, 2003.
Includes bibliographical references (p. 116-126).
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Mode of access: World Wide Web.
Abstracts in English and Chinese.
Capítulos de libros sobre el tema "Synthetic Self-assembling Amino Acid"
Tang, Ben Zhong, Kevin K. L. Cheuk, Fouad Salhi, Bingshi Li, Jacky W. Y. Lam, John A. K. Cha y Xudong Xiao. "Synthesis, Helical Chirality, and Self-Assembling Hierarchical Structures of Amino Acid-Containing Polyacetylenes". En ACS Symposium Series, 133–48. Washington, DC: American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0812.ch010.
Texto completoHaspel, Nurit, Jie Zheng, Carlos Aleman, David Zanuy y Ruth Nussinov. "A Protocol for the Design of Protein and Peptide Nanostructure Self-Assemblies Exploiting Synthetic Amino Acids". En Methods in Molecular Biology, 323–52. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6637-0_17.
Texto completoMeldal, Morten y Robert C. Sheppard. "ESTERS OF FMOC-AMINO ACIDS WITH 3,4,-DIHYDRO-3-HYDROXY-4-OXO-1,2,3-BENZOTRIAZINE. A NEW CLASS OF SELF-INDICATING, ACTIVATED INTERMEDIATES FOR SOLID PHASE SYNTHESIS". En Porto Carras, Chalkidiki, Greece, Aug. 31–Sept. 5, 1986, editado por Dimitrios Theodoropoulos, 131–34. Berlin, Boston: De Gruyter, 1987. http://dx.doi.org/10.1515/9783110864243-027.
Texto completoChhabra, Seema, Smrity Sahu, Keshav Sharma, Maryada Sharma, Lekha Rani, Ranjana Minz y Sunil Dogra. "Th17/IL-17, Immunometabolism and Psoriatic Disease: A Pathological Trifecta". En Psoriasis [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.102633.
Texto completoActas de conferencias sobre el tema "Synthetic Self-assembling Amino Acid"
Han, Sang-Cheol, Kwang-Min Choi y Sang-Eon Park. "Facile Synthesis of Mesoporous Silica Nanotubes With Amide Type Surfactant". En ASME 2008 2nd Multifunctional Nanocomposites and Nanomaterials International Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/mn2008-47070.
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