Relevant bibliographies by topics / Proteoliposome transporter

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Proteoliposome transporter'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Proteoliposome transporter"

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Cosco, Jessica, Teresa M. R. Regina, Mariafrancesca Scalise, Michele Galluccio, and Cesare Indiveri. "Regulatory Aspects of the Vacuolar CAT2 Arginine Transporter of S. lycopersicum: Role of Osmotic Pressure and Cations." International Journal of Molecular Sciences 20, no. 4 (2019): 906. http://dx.doi.org/10.3390/ijms20040906.

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Many proteins are localized at the vacuolar membrane, but most of them are still poorly described, due to the inaccessibility of this membrane from the extracellular environment. This work focused on the characterization of the CAT2 transporter from S. lycopersicum (SlCAT2) that was previously overexpressed in E. coli and reconstituted in proteoliposomes for transport assay as [3H]Arg uptake. The orientation of the reconstituted transporter has been attempted and current data support the hypothesis that the protein is inserted in the liposome in the same orientation as in the vacuole. SlCAT2 a
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Pochini, Lorena, Gilda Pappacoda, Michele Galluccio, Francesco Pastore, Mariafrancesca Scalise, and Cesare Indiveri. "Effect of Cholesterol on the Organic Cation Transporter OCTN1 (SLC22A4)." International Journal of Molecular Sciences 21, no. 3 (2020): 1091. http://dx.doi.org/10.3390/ijms21031091.

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The effect of cholesterol was investigated on the OCTN1 transport activity measured as [14C]-tetraethylamonium or [3H]-acetylcholine uptake in proteoliposomes reconstituted with native transporter extracted from HeLa cells or the human recombinant OCTN1 over-expressed in E. coli. Removal of cholesterol from the native transporter by MβCD before reconstitution led to impairment of transport activity. A similar activity impairment was observed after treatment of proteoliposomes harboring the recombinant (cholesterol-free) protein by MβCD, suggesting that the lipid mixture used for reconstitution
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Hakim Elahi, Sepideh, Morteza Abbaszadegan, and Otakuye Conroy-Ben. "Engineered proteoliposome transporter for treatment of cesium contaminated water." Science of The Total Environment 704 (February 2020): 135317. http://dx.doi.org/10.1016/j.scitotenv.2019.135317.

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Wan, Hao, Chengfeng Merriman, Mark A. Atkinson, et al. "Proteoliposome-based full-length ZnT8 self-antigen for type 1 diabetes diagnosis on a plasmonic platform." Proceedings of the National Academy of Sciences 114, no. 38 (2017): 10196–201. http://dx.doi.org/10.1073/pnas.1711169114.

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Identified as a major biomarker for type 1 diabetes (T1D) diagnosis, zinc transporter 8 autoantibody (ZnT8A) has shown promise for staging disease risk and disease diagnosis. However, existing assays for ZnT8 autoantibody (ZnT8A) are limited to detection by soluble domains of ZnT8, owing to difficulties in maintaining proper folding of a full-length ZnT8 protein outside its native membrane environment. Through a combined bioengineering and nanotechnology approach, we have developed a proteoliposome-based full-length ZnT8 self-antigen (full-length ZnT8 proteoliposomes; PLR-ZnT8) for efficient d
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Rajagopalan, Nandhakishore, Annamaria Halasz, Yuping Lu, Enwu Liu, Fanny Monteil-Rivera, and Michele C. Loewen. "Probing allocrite preferences of 2 naturally occurring variants of the wheat LR34 ABC transporter." Biochemistry and Cell Biology 94, no. 5 (2016): 459–70. http://dx.doi.org/10.1139/bcb-2016-0058.

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For almost a century, the wheat Lr34 gene has conferred durable resistance against fungal rust diseases. While sequence homology predicts a putative ATP binding cassette transporter, the molecules that are transported (allocrites) by the encoded LR34 variants, and any associated mechanism of resistance, remain enigmatic. Here, the in vitro transport characteristics of 2 naturally occurring Lr34 variants (that differ in their ability to mediate disease resistance; Lr34sus and Lr34res) are investigated. Initially, a method to express and purify recombinant LR34Sus and LR34Res pseudo half-molecul
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Togawa, Natsuko, Narinobu Juge, Takaaki Miyaji, Miki Hiasa, Hiroshi Omote, and Yoshinori Moriyama. "Wide expression of type I Na+-phosphate cotransporter 3 (NPT3/SLC17A2), a membrane potential-driven organic anion transporter." American Journal of Physiology-Cell Physiology 309, no. 2 (2015): C71—C80. http://dx.doi.org/10.1152/ajpcell.00048.2015.

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Membrane potential (Δψ)-driven and Cl−-dependent organic anion transport is a primary function of the solute carrier family 17 (SLC17) transporter family. Although the transport substrates and physiological relevance of the major members are well understood, SLC17A2 protein known to be Na+-phosphate cotransporter 3 (NPT3) is far less well characterized. In the present study, we investigated the transport properties and expression patterns of mouse SLC17A2 protein (mNPT3). Proteoliposomes containing the purified mNPT3 protein took up radiolabeled p-aminohippuric acid (PAH) in a Δψ- and Cl−-depe
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Rautengarten, Carsten, Devon Birdseye, Sivakumar Pattathil, et al. "The elaborate route for UDP-arabinose delivery into the Golgi of plants." Proceedings of the National Academy of Sciences 114, no. 16 (2017): 4261–66. http://dx.doi.org/10.1073/pnas.1701894114.

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In plants, L-arabinose (Ara) is a key component of cell wall polymers, glycoproteins, as well as flavonoids, and signaling peptides. Whereas the majority of Ara found in plant glycans occurs as a furanose ring (Araf), the activated precursor has a pyranose ring configuration (UDP-Arap). The biosynthesis of UDP-Arap mainly occurs via the epimerization of UDP-xylose (UDP-Xyl) in the Golgi lumen. Given that the predominant Ara form found in plants is Araf, UDP-Arap must exit the Golgi to be interconverted into UDP-Araf by UDP-Ara mutases that are located outside on the cytosolic surface of the Go
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Chin, J. J., E. K. Jung, V. Chen, and C. Y. Jung. "Structural basis of human erythrocyte glucose transporter function in proteoliposome vesicles: circular dichroism measurements." Proceedings of the National Academy of Sciences 84, no. 12 (1987): 4113–16. http://dx.doi.org/10.1073/pnas.84.12.4113.

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Boadu, Emmanuel, and Georg Sager. "ATPase activity and transport by a cGMP transporter in human erythrocyte ghosts and proteoliposome-reconstituted membrane extracts." Biochimica et Biophysica Acta (BBA) - Biomembranes 1509, no. 1-2 (2000): 467–74. http://dx.doi.org/10.1016/s0005-2736(00)00328-x.

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Tonazzi, Annamaria, Ivano Eberini, and Cesare Indiveri. "Molecular Mechanism of Inhibition of the Mitochondrial Carnitine/Acylcarnitine Transporter by Omeprazole Revealed by Proteoliposome Assay, Mutagenesis and Bioinformatics." PLoS ONE 8, no. 12 (2013): e82286. http://dx.doi.org/10.1371/journal.pone.0082286.

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Dissertations / Theses on the topic "Proteoliposome transporter"

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Chao, Chih-Kai. "The vesicular glutamate transporter (VGLUT): heterologous expression, proteoliposome, computational and mass spectral studies." The University of Montana, 2009. http://etd.lib.umt.edu/theses/available/etd-12112008-140102/.

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<P>Vesicular glutamate transporters (VGLUTs) are integral membrane proteins that uptake glutamate into synaptic vesicles and are involved in glutamatergic neurotransmission. Since VGLUTs were identified and cloned, efforts have been made to characterize their functional roles. However, due to experimental limitations, the structural features of VGLUT protein remain unclear. In an attempt to better understand VGLUTs, computational and biochemical approaches were employed to characterize them. Plasmid DNA encoding rat VGLUT1 was constructed, amplified and expressed in Pichia pastoris to produce
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Chao, Chih-Kai. "The vesicular glutamate transporter (VGLUT) heterologous expression, proteoliposome, computational and mass spectral studies /." CONNECT TO THIS TITLE ONLINE, 2008. http://etd.lib.umt.edu/theses/available/etd-12112008-140102/.

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Peterson, Emily. "Proteoliposome Proton Flux Assays Establish Net Conductance, pH-Sensitivity, and Functional Integrity of a Novel Truncate of the M2 Ion "Channel" of Influenza A." BYU ScholarsArchive, 2010. https://scholarsarchive.byu.edu/etd/2420.

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A novel truncate of Influenza A M2 protein (residues 22-62), incorporated into a uniquely tailored proteoliposome proton uptake assay, demonstrated proton flux more characteristic of an ion transporter than a traditional ion "channel." The liposome paradigm was essential for testing the conductance activity of this M2 truncate at a range of extraphysiological pHs appropriate for channel vs. transport function determination. In addition to transporter-typical proton flux, M2(22-62) showed the key characteristics of functional integrity: selective proton uptake into liposomes and block of uptake
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Zuo, Shusheng. "Quantitation, Purification and Reconstitution of the Red Blood Cell Glucose Transporter GLUT1." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ-bibl. [distributör], 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-5727.

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Lagerquist, Hägglund Christine. "Affinity-, Partition- and Permeability Properties of the Human Red Blood Cell Membrane and Biomembrane Models, with Emphasis on the GLUT1 Glucose Transporter." Doctoral thesis, Uppsala University, Department of Biochemistry, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3525.

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<p>The human glucose transporter GLUT1 is abundant in red blood cells, the blood-brain barrier and epithelial cells, where it mediates the transport of the energy metabolite, glucose. In the present work some properties of GLUT1, including affinity binding of both substrates and inhibitors, transport rates as well as permeabilities of aromatic amino acids and drug-membrane interactions were analyzed by chromatographic methods.</p><p>Reconstitution by size-exclusion chromatography on Superdex 75 from a detergent with a low CMC that provides monomeric GLUT1 was examined regarding D-glucose- and
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Galian, Barrueco Carmen. "Caractérisation de 2 transporteurs ABC (“ATP-Binding Cassette”) bactériens de fonction inconnue : YheI/YheH de Bacillus subtilis et Rv1747 de Mycobacterium tuberculosis." Phd thesis, Grenoble 1, 2008. http://tel.archives-ouvertes.fr/tel-00369447.

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L'émergence du phénotype MDR (« multidrug resistance») des cellules cancéreuses est souvent corrélée à la surexpression de protéines membranaires appartenant à la superfamille ABC (« ATP binding cassette »). Ces protéines couplent l'hydrolyse de l'ATP au transport d'agents chimiothérapeutiques vers l'extérieur des cellules. Chez les bactéries, des transporteurs homologues ont été impliqués dans certains cas de résistance aux antibiotiques.<br />Deux nouveaux transporteurs ABC bactériens, Rv1747 de Mycobacterium tuberculosis et YheI/YheH de Bacillus subtilis, potentiellement impliqués dans la r
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Verchère, Alice. "Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa." Thesis, Paris 5, 2014. http://www.theses.fr/2014PA05P622/document.

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L’efflux actif, qui permet aux bactéries d’exporter les antibiotiques vers le milieu extérieur est l’un des mécanismes majeurs de résistance aux antibiotiques. L’une des pompes d’efflux de Pseudomonas aeruginosa, MexA-MexB-OprM, est constituée de trois protéines : i) MexA, une protéine membranaire de fusion qui se trouve dans le périplasme ; ii) MexB qui se trouve dans la membrane interne et qui reconnaît l’antibiotique et initie son transport grâce à la force protomotrice et iii) OprM un canal qui se trouve dans la membrane externe. Durant ma thèse, j’ai mis au point un test fonctionnel pour
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"Engineering a Proteoliposome Transporter to Capture Radioactive Cesium from Water." Doctoral diss., 2018. http://hdl.handle.net/2286/R.I.51692.

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abstract: Radioactive cesium (137Cs), released from nuclear power plants and nuclear accidental releases, is a problem due to difficulties regarding its removal. Efforts have been focused on removing cesium and the remediation of the contaminated environment. Traditional treatment techniques include Prussian blue and nano zero-valent ion (nZVI) and nano-Fe/Cu particles to remove Cs from water; however, they are not efficient at removing Cs when present at low concentrations of about 10 parts-per-billion (ppb), typical of concentrations found in the radioactive contaminated sites. The objecti
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Akik, Wided. "Étude de la perméabilité intestinale des médicaments par la reconstitution du transporteur BCRP/ABCG2 dans des protéoliposomes." Thèse, 2017. http://hdl.handle.net/1866/20545.

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Flandrin, Aurore. "Mise en place d’un nouveau test de perméabilité membranaire à l’aide de la glycoprotéine-P reconstituée dans des protéoliposomes." Thèse, 2016. http://hdl.handle.net/1866/19169.

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Les membranes cellulaires jouent un rôle important dans l’absorption des médicaments et la distribution de ceux-ci dans le corps humain. Elles contiennent différents transporteurs membranaires qui sont responsables des profils pharmacocinétiques, d’innocuité et d’efficacité des xénobiotiques. Lors du développement d’un médicament, il s’avère donc indispensable, de prédire l’interaction des nouveaux composés avec les transporteurs présents dans l’organisme. Le but du projet de recherche est de créer un nouvel outil pour étudier le comportement de la glycoprotéine-P (P-gp), un transporteur membr
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Books on the topic "Proteoliposome transporter"

1

Lundqvist, Andreas. Chromatographic Characterization of the Human Red Cell Glucose Transporter Glut1 in the Cells, in Membrane Vesicles and in Proteoliposomes. Uppsala Universitet, 1999.

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Book chapters on the topic "Proteoliposome transporter"

1

Console, Lara, Maria Tolomeo, and Cesare Indiveri. "Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1286-6_4.

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Driessen, Arnold J. M., Klaas J. Hellingwerf, and Wil N. Konings. "Light Induced Generation of a Proton Motive Force and Ca++-Transport in Membrane Vesicles of Streptococcus Cremoris Fused with Bacteriorhodopsin Proteoliposomes." In Recent Advances in Biological Membrane Studies. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4979-2_26.

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