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Статті в журналах з теми "Membrance domains"
Dale, B., E. Tosti, and M. Iaccarino. "Is the plasma membrane of the human oocyte reorganised following fertilisation and early cleavage?" Zygote 3, no. 1 (February 1995): 31–36. http://dx.doi.org/10.1017/s0967199400002355.
Повний текст джерелаSnead, Wilton T., Wade F. Zeno, Grace Kago, Ryan W. Perkins, J. Blair Richter, Chi Zhao, Eileen M. Lafer, and Jeanne C. Stachowiak. "BAR scaffolds drive membrane fission by crowding disordered domains." Journal of Cell Biology 218, no. 2 (November 30, 2018): 664–82. http://dx.doi.org/10.1083/jcb.201807119.
Повний текст джерелаGallop, Jennifer L., and Harvey T. McMahon. "BAR domains and membrane curvature: bringing your curves to the BAR." Biochemical Society Symposia 72 (January 1, 2005): 223–31. http://dx.doi.org/10.1042/bss0720223.
Повний текст джерелаGolantsova, Nina E., Elena E. Gorbunova, and Erich R. Mackow. "Discrete Domains within the Rotavirus VP5* Direct Peripheral Membrane Association and Membrane Permeability." Journal of Virology 78, no. 4 (February 15, 2004): 2037–44. http://dx.doi.org/10.1128/jvi.78.4.2037-2044.2004.
Повний текст джерелаChowdary, Tirumala Kumar, and Ekaterina E. Heldwein. "Syncytial Phenotype of C-Terminally Truncated Herpes Simplex Virus Type 1 gB Is Associated with Diminished Membrane Interactions." Journal of Virology 84, no. 10 (March 3, 2010): 4923–35. http://dx.doi.org/10.1128/jvi.00206-10.
Повний текст джерелаYamamoto, Eiji, Jan Domański, Fiona B. Naughton, Robert B. Best, Antreas C. Kalli, Phillip J. Stansfeld, and Mark S. P. Sansom. "Multiple lipid binding sites determine the affinity of PH domains for phosphoinositide-containing membranes." Science Advances 6, no. 8 (February 2020): eaay5736. http://dx.doi.org/10.1126/sciadv.aay5736.
Повний текст джерелаKarotki, Lena, Juha T. Huiskonen, Christopher J. Stefan, Natasza E. Ziółkowska, Robyn Roth, Michal A. Surma, Nevan J. Krogan, et al. "Eisosome proteins assemble into a membrane scaffold." Journal of Cell Biology 195, no. 5 (November 28, 2011): 889–902. http://dx.doi.org/10.1083/jcb.201104040.
Повний текст джерелаPennington, Edward Ross, E. Madison Sullivan, Amy Fix, Sahil Dadoo, Tonya N. Zeczycki, Anita DeSantis, Uwe Schlattner, et al. "Proteolipid domains form in biomimetic and cardiac mitochondrial vesicles and are regulated by cardiolipin concentration but not monolyso-cardiolipin." Journal of Biological Chemistry 293, no. 41 (August 29, 2018): 15933–46. http://dx.doi.org/10.1074/jbc.ra118.004948.
Повний текст джерелаMa, Alice D., Lawrence F. Brass, and Charles S. Abrams. "Pleckstrin Associates with Plasma Membranes and Induces the Formation of Membrane Projections: Requirements for Phosphorylation and the NH2-terminal PH Domain." Journal of Cell Biology 136, no. 5 (March 10, 1997): 1071–79. http://dx.doi.org/10.1083/jcb.136.5.1071.
Повний текст джерелаGILLOOLY, David J., Anne SIMONSEN, and Harald STENMARK. "Cellular functions of phosphatidylinositol 3-phosphate and FYVE domain proteins." Biochemical Journal 355, no. 2 (April 6, 2001): 249–58. http://dx.doi.org/10.1042/bj3550249.
Повний текст джерелаДисертації з теми "Membrance domains"
Gutlederer, Erwin Johann. "On the morphology of vesicles. - [überarb. Diss.]." Universität Potsdam, 2007. http://opus.kobv.de/ubp/volltexte/2007/1506/.
Повний текст джерелаDie vorliegende Arbeit enthält theoretische Untersuchungen zur Morphologie und statistischen Mechanik von Vesikeln. Es wird die Gestalt homogener fluider Vesikel und inhomogener Vesikel mit fluiden und festen Membrandomänen berechnet. Der Einfluss thermischer Fluktuationen wird untersucht. Die erzielten Ergebnisse beziehen sich auf mesoskopische Längenskalen und basieren auf einem geometrischen Membranmodell, in welchem die Vesikelmembran als statische, beziehungsweise thermisch fluktuierende Fläche beschrieben wird. Die Arbeit besteht aus drei Teilen. Im ersten Teil werden homogene fluide Vesikel betrachtet. Das Interesse gilt dem thermisch induzierten Morphologieübergang zwischen prolaten und oblaten Vesikelformen. Mit Hilfe von Monte-Carlo-Simulationen wird ein freies Energieprofil für diese Vesikel ermittelt. Es kann gezeigt werden, dass die Formumwandlung zwischen prolaten und oblaten Formen kontinuierlich verläuft und mit keiner freien Energiebarriere verbunden ist. Der zweite und dritte Teil beschäftigt sich mit inhomogenen Vesikeln, die intramembrane Domänen enthalten. Ausgangspunkt und Motivation der Berechnungen sind experimentelle Studien über Domänbildung in ein- oder mehrkomponentigen Vesikelmembranen, bei denen Phasentrennung stattfindet und unterschiedliche Membranphasen koexistieren. Die dabei auftretenden Domänen unterscheiden sich hinsichtlich ihrer Membranstruktur (fest, fluid). Diese beeinflusst die Form der Domäne und des gesamten Vesikels auf entscheidende Weise. Im zweiten Teil werden Vesikel untersucht, bei denen feste und fluide Membrandomänen koexistieren, Teil drei widmet sich Vesikeln mit zwei koexistierenden fluiden Membranphasen. In Abhängigkeit von Materialparametern werden durch Minimierung der Membranenergie die Grundzustandsformen von Vesikeln mit einfachen und komplexen Domänenformen bestimmt. Die Ergebnisse werden in Morphologiediagrammen zusammengefasst. Dabei werden bisher unbekannte Morphologieübergänge zwischen Vesikeln mit unterschiedlichen Domänformen beobachtet. Die Auswirkungen thermischer Fluktuationen auf die Vesikel und die Form ihrer Domänen werden mittels Monte-Carlo-Simulationen untersucht.
Oldham, Alexis Jean. "Modulation of lipid domain formation in mixed model systems by proteins and peptides." View electronic thesis, 2008. http://dl.uncw.edu/etd/2008-1/r1/oldhama/alexisoldham.pdf.
Повний текст джерелаWilkinson, Debbie Isabelle. "Visualisation of osteoclast membrane domains." Thesis, University of Aberdeen, 2010. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=158808.
Повний текст джерелаDaste, Frédéric. "Function and regulation of coiled‐coil domains in intracellular membrane fusion." Thesis, Sorbonne Paris Cité, 2015. http://www.theses.fr/2015PA05T001.
Повний текст джерелаThe molecular mechanisms involved in membrane fusion have been extensively studied for the past thirty years. Our current understanding of this phenomenon is mainly based on results obtained by (i) the development of physical models describing the fusion of membranes, (ii) structural and mechanistic investigations on fusion proteins of enveloped viruses and (iii) studies of SNARE protein-mediated intracellular fusion events of eukaryotic cells. Discovery of the SNARE complex was the outcome of interdisciplinary works which involved a wide range of techniques including yeast genetics, electrophysiology, molecular biology, cell-free biochemistry, adhesion/fusion biophysics and imaging. Taking advantage of the paradigms and biophysical techniques that emerged from these studies, we investigated the function and regulation of coiled-coil domains in intracellular fusion processes involving Longin-SNAREs or Mitofusins, two fusion protein machineries whose exact mode of action still remains unclear. A comprehensive understanding of the molecular mechanisms of membrane fusion requires the in vitro reconstitution of fusion proteins into a wide variety of membrane environments with defined and tunable biophysical properties. Ideally, these membrane systems should allow the experimentalists to control the lipid and protein composition as well as the membrane topology, to account for the variability observed across cellular fusing compartments. Reconstitution into liposomes offers amazing flexibility with the capacity to vary most of these relevant parameters, and to create a minimal environment in which membrane and/or soluble factors can be added, one at a time or in combination, to reveal their role with clarity. We have set up the in vitro reconstitution of proteins into various artificial membrane platforms for both systems (the Longin-SNAREs TI-VAMP and Sec22b and the coiled-coil domains of Mitofusins) and performed biochemical assays to gain insight into how these proteins execute their functions. The long-term goal of this project is to compare the molecular mechanisms of SNARE and Mitofusin fusion machineries and thus reveal structural and functional similitudes between (i) their core fusion proteins, and (ii) their regulatory factors
Jean-François, Frantz. "Vers un nouveau mode d’action de peptides antimicrobiens structurés en feuillets ß : formation de domaines membranaires par la cateslytine." Thesis, Bordeaux 1, 2008. http://www.theses.fr/2008BOR13638/document.
Повний текст джерелаThe antimicrobial peptide Cateslytin (bCGA RSMRLSFRARGYGFR ) is a five positively charged arginin rich peptide known to inhibit the release of catecholamine in chromaffin granules. Although biological data showed that it is able to inhibit the growth of several microorganisms such as bacteria, yeast and Plasmodium falciparum parasite involved in malaria, the mechanism of action has not been yet studied. In order to better understand both targeting and selectivity of this peptide towards microorganisms, model membranes of variable compositions have been chosen to respectively mimic microorganisms or mammalian membranes. Structural studies have been performed using polarised ATR-FTIR, circular dichroïsm and high resolution NMR Membrane dynamics has been followed using deuterium labelled lipids and solid state NMR Patch clamp experiments were also performed on lipid vesicles to measure channe conductivity. All-atom molecular dynamics on hydrated peptide-lipid membrane systems was also used to assess the interaction from the atomic level. Main results from this interdisciplinary approach are three-fold. i) Electric current passages through membranes demonstrate permeation akin to pore formation. ii) Peptide-induced formation of rigid domains mainly made of negatively charged lipids is found. iii) Peptide antiparallel ß-sheets are observed preferentially with negatively charged lipids mimicking microorganism membranes. The general picture leads to the proposal that membrane destabilization/permeation is promoted by rigid domains stabilised by peptide ß-sheets
Goulding, Rebecca Ellen. "Membrane localization of RasGRPs by C1 domains." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/24211.
Повний текст джерелаHeadlam, Madeleine Joyce. "Cytochrome P450scc (CYP11A1) : effects of glycerol and identification of the membrane binding domain." University of Western Australia. School of Biomedical and Chemical Sciences, 2004. http://theses.library.uwa.edu.au/adt-WU2004.0065.
Повний текст джерелаSalkhordeh, Mahmoud. "Localization of membrane binding domains in synapsin I." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ57790.pdf.
Повний текст джерелаSalkhordeh, Mahmoud Carleton University Dissertation Biology. "Localization of membrane binding domains in synapsin I." Ottawa, 2000.
Знайти повний текст джерелаBrechin, C. "14-3-3 proteins and cholesterol-dependent membrane domains." Thesis, University of Edinburgh, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641914.
Повний текст джерелаКниги з теми "Membrance domains"
J, Quinn P., ed. Membrane dynamics and domains. Dordrecht: Kluwer Academic/Plenum, 2004.
Знайти повний текст джерелаCellular domains. Hoboken, N.J: Wiley-Blackwell, 2011.
Знайти повний текст джерелаQuinn, Peter J., ed. Membrane Dynamics and Domains. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1.
Повний текст джерелаK, Tamm Lukas, ed. Protein-lipid interactions: From membrane domains to cellular networks. Weinheim: Wiley-VCH, 2005.
Знайти повний текст джерелаSaleh, Mazen T. Identifying domains of Shiga-like toxin I that are responsible for its membrane translocation. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1997.
Знайти повний текст джерелаKarlsson, Jenny. Functional and structural analysis of the membrane domain of proton-translocating Escherichia coli Transhydrogenase. Göteborg: Department of Chemistry, Biochemistry and Physices, Göteborg University, 2006.
Знайти повний текст джерелаC, Aloia Roland, Curtain Cyril C, and Gordon Larry M, eds. Lipid domains and the relationship to membrane function. New York: Liss, 1988.
Знайти повний текст джерелаKusumi, Akihiro, and Takahiro Fujiwara. Plasma Membrane Domains. Morgan & Claypool Life Science Publishers, 2012.
Знайти повний текст джерелаNabi, Ivan R. Cellular Domains. Wiley & Sons, Incorporated, John, 2011.
Знайти повний текст джерелаNabi, Ivan R. Cellular Domains. Wiley & Sons, Incorporated, John, 2011.
Знайти повний текст джерелаЧастини книг з теми "Membrance domains"
Coombs, Daniel, Raibatak Das, and Jennifer S. Morrison. "Modeling Membrane Domains." In Cellular Domains, 71–84. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118015759.ch5.
Повний текст джерелаWolf, Claude, and Peter J. Quinn. "Membrane Lipid Homeostasis." In Membrane Dynamics and Domains, 317–57. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_10.
Повний текст джерелаMeiri, Karina F. "Membrane/Cytoskeleton Communication." In Membrane Dynamics and Domains, 247–82. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_8.
Повний текст джерелаOliver, Janet M., Janet R. Pfeiffer, Zurab Surviladze, Stanly L. Steinberg, Karin Leiderman, Margaret L. Sanders, Carla Wofsy, et al. "Membrane Receptor Mapping: The Membrane Topography of FcεRI Signaling." In Membrane Dynamics and Domains, 3–34. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_1.
Повний текст джерелаVeldhuizen, Ruud, and Fred Possmayer. "Phospholipid Metabolism in Lung Surfactant." In Membrane Dynamics and Domains, 359–88. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_11.
Повний текст джерелаSchrader, Michael. "Membrane Targeting in Secretion." In Membrane Dynamics and Domains, 391–421. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_12.
Повний текст джерелаParat, Marie-Odile, and Paul L. Fox. "Oxidative Stress, Caveolae and Caveolin-1." In Membrane Dynamics and Domains, 425–41. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_13.
Повний текст джерелаNayak, Debi P., and Eric K. W. Hui. "The Role of Lipid Microdomains in Virus Biology." In Membrane Dynamics and Domains, 443–91. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_14.
Повний текст джерелаMorris, Roger, Helen Cox, Enrico Mombelli, and Peter J. Quinn. "Rafts, Little Caves and Large Potholes: How Lipid Structure Interacts with Membrane Proteins to Create Functionally Diverse Membrane Environments." In Membrane Dynamics and Domains, 35–118. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_2.
Повний текст джерелаWollscheid, Bernd, Priska D. von Haller, Eugene Yi, Samuel Donohoe, Kelly Vaughn, Andrew Keller, Alexey I. Nesvizhskii, et al. "Lipid Raft Proteins and Their Identification in T Lymphocytes." In Membrane Dynamics and Domains, 121–52. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-5806-1_3.
Повний текст джерелаТези доповідей конференцій з теми "Membrance domains"
Shao, Jianwang, Xian Wu, and Bruno Cochelin. "Study of Targeted Energy Transfer Inside 3D Acoustic Cavity by Two Nonlinear Membrane Absorbers." In ASME 2015 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/detc2015-46227.
Повний текст джерелаTabouillot, Tristan, Hari S. Muddana, and Peter J. Butler. "Shear Stress Induces Time- and Domain-Dependent Changes in Lipid Dynamics of Endothelial Cell Membranes." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206882.
Повний текст джерелаLee, Chi-Hung, Jia-Ru Chen, Hung-Wei Shiu, Ko-Shan Ho, Shinn-Dar Wu, Kuo-Huang Hsieh, and Yen-Zen Wang. "Effect of Bridging Groups on Sulfonated Poly(Imide-Siloxane) for Application in Proton Exchange Membrane of Fuel Cells." In ASME 2008 6th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2008. http://dx.doi.org/10.1115/fuelcell2008-65155.
Повний текст джерелаKalyan, N. K., S. G. Lee, W.-T. Hum, R. Hartzell, M. Levner, and P. P. Hung. "IN VITRO STUDIES ON THE BINDING OF TISSUE-TYPE PLASMINOGEN ACTIVATOR (t-PA) AND UROKINASE (u-PA) TO LIVER MEMBRANES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643603.
Повний текст джерелаGurau, Vladimir, Sadik Kakaç, and Hongtan Liu. "Mathematical Model for Proton Exchange Membrane Fuel Cells." In ASME 1998 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1998. http://dx.doi.org/10.1115/imece1998-0845.
Повний текст джерелаUsta, Mustafa, Ali E. Anqi, Michael Morabito, Alaa Hakim, Mohammed Alrehili, and Alparslan Oztekin. "Computational Study of Reverse Osmosis Desalination Process: Hollow Fiber Module." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-70884.
Повний текст джерелаJiang, Yanfei, Guy M. Genin, Srikanth Singamaneni, and Elliot L. Elson. "Interfacial Phases on Giant Unilamellar Vesicles." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80942.
Повний текст джерелаRomero, T., and W. Me´rida. "Transient Water Transport in Nafion Membranes Under Activity Gradients." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33317.
Повний текст джерелаJahangiri Mamouri, Sina, Volodymyr V. Tarabara, and André Bénard. "Numerical Simulation of Filtration of Charged Oil Particles in Stationary and Rotating Tubular Membranes." In ASME 2015 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/imece2015-52038.
Повний текст джерелаSwickrath, Michael J., Kevin Dorfman, Yoav Segal, and Victor H. Barocas. "The Effect of Composition and Inter- and Intrafibrillar Interactions on the Structure of Collagen IV Networks in the Computer-Simulated Glomerular Basement Membrane." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-205518.
Повний текст джерелаЗвіти організацій з теми "Membrance domains"
Shai, Yechiel, Arthur Aronson, Aviah Zilberstein, and Baruch Sneh. Study of the Basis for Toxicity and Specificity of Bacillus thuringiensis d-Endotoxins. United States Department of Agriculture, January 1996. http://dx.doi.org/10.32747/1996.7573995.bard.
Повний текст джерелаWisniewski, Michael, Samir Droby, John Norelli, Dov Prusky, and Vera Hershkovitz. Genetic and transcriptomic analysis of postharvest decay resistance in Malus sieversii and the identification of pathogenicity effectors in Penicillium expansum. United States Department of Agriculture, January 2012. http://dx.doi.org/10.32747/2012.7597928.bard.
Повний текст джерелаMevarech, Moshe, Jeremy Bruenn, and Yigal Koltin. Virus Encoded Toxin of the Corn Smut Ustilago Maydis - Isolation of Receptors and Mapping Functional Domains. United States Department of Agriculture, September 1995. http://dx.doi.org/10.32747/1995.7613022.bard.
Повний текст джерелаBrown, Deborah A. The Role of Spingolipid- and Cholesterol-Rich Membrane Domains in Pathophysiology of Cultured Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2001. http://dx.doi.org/10.21236/ada395838.
Повний текст джерелаBrown, Deborah A. The Role of Sphingolipid-and Cholesterol-Rich Membrane Domains in Pathophysiology and Cultured Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2004. http://dx.doi.org/10.21236/ada431301.
Повний текст джерелаBrown, Deborah A. The Role of Sphingolipid- and Cholesterol-Rich Membrane Domains in Pathophsiology of Cultured Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2003. http://dx.doi.org/10.21236/ada421916.
Повний текст джерелаOliver, Janet, Janet Pfeiffer, Bridget Wilson, and Alan Richard Burns. Studies of signaling domains in model and biological membranes through advanced imaging techniques: final report. US: Sandia National Laboratories, October 2006. http://dx.doi.org/10.2172/894746.
Повний текст джерелаYordanova, Vesela, Galya Staneva, Miglena Angelova, Victoria Vitkova, Aneliya Kostadinova, Dayana Benkova, Ralitsa Veleva, and Rusina Hazarosova. Modelling of Molecular Mechanisms of Membrane Domain Formation during the Oxidative Stress: Effect of Palmitoyl-oxovaleroyl-phosphatidylcholine. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, January 2021. http://dx.doi.org/10.7546/crabs.2021.01.10.
Повний текст джерелаZilberstein, Aviah, Bo Liu, and Einat Sadot. Studying the Involvement of the Linker Protein CWLP and its Homologue in Cytoskeleton-plasma Membrane-cell Wall Continuum and in Drought Tolerance. United States Department of Agriculture, June 2012. http://dx.doi.org/10.32747/2012.7593387.bard.
Повний текст джерелаMcElwain, Terry, Eugene Pipano, Guy Palmer, Varda Shkap, Stephen Hines, and Douglas Jasmer. Protection of Cattle Against Babesiosis: Immunization with Recombinant DNA Derived Apical Complex Antigens of Babesia bovis. United States Department of Agriculture, June 1995. http://dx.doi.org/10.32747/1995.7612835.bard.
Повний текст джерела