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Commentary & View

PrP assemblies

Spotting the responsible regions in Prion propagation

&
Pages 69-75 | Received 02 Mar 2011, Accepted 09 May 2011, Published online: 01 Apr 2011

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Suman Pal & Jayant B. Udgaonkar. (2023) Mutations of evolutionarily conserved aromatic residues suggest that misfolding of the mouse prion protein may commence in multiple ways. Journal of Neurochemistry 167:5, pages 696-710.
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Alexandra Louka, Elsa Zacco, Piero Andrea Temussi, Gian Gaetano Tartaglia & Annalisa Pastore. (2020) RNA as the stone guest of protein aggregation. Nucleic Acids Research 48:21, pages 11880-11889.
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Concetta Di Natale, Sara La Manna, Concetta Avitabile, Daniele Florio, Giancarlo Morelli, Paolo Antonio Netti & Daniela Marasco. (2020) Engineered β-hairpin scaffolds from human prion protein regions: Structural and functional investigations of aggregates. Bioorganic Chemistry 96, pages 103594.
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Chafik Harrathi, Natalia Fernández-Borges, Hasier Eraña, Saioa R. Elezgarai, Vanessa Venegas, Jorge M. Charco & Joaquín Castilla. (2018) Insights into the Bidirectional Properties of the Sheep–Deer Prion Transmission Barrier. Molecular Neurobiology 56:8, pages 5287-5303.
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Holger Wille, Lyudmyla Dorosh, Sara Amidian, Gerold Schmitt-Ulms & Maria Stepanova. 2019. Protein Misfolding. Protein Misfolding 33 110 .
Hasier Eraña, Natalia Fernández-Borges, Saioa R. Elezgarai, Chafik Harrathi, Jorge M. Charco, Francesca Chianini, Mark P. Dagleish, Gabriel Ortega, Óscar Millet & Joaquín Castilla. (2017) In Vitro Approach To Identify Key Amino Acids in Low Susceptibility of Rabbit Prion Protein to Misfolding . Journal of Virology 91:24.
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Aurora Armiento, Philippe Moireau, Davy Martin, Nad’a Lepejova, Marie Doumic & Human Rezaei. (2017) The mechanism of monomer transfer between two structurally distinct PrP oligomers. PLOS ONE 12:7, pages e0180538.
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Guillaume Van der Rest, Human Rezaei & Frédéric Halgand. (2016) Monitoring Conformational Landscape of Ovine Prion Protein Monomer Using Ion Mobility Coupled to Mass Spectrometry. Journal of the American Society for Mass Spectrometry 28:2, pages 303-314.
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S. Alexis Paz, Eric Vanden-Eijnden & Cameron F. Abrams. (2017) Polymorphism at 129 dictates metastable conformations of the human prion protein N-terminal β-sheet. Chemical Science 8:2, pages 1225-1232.
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E. Vázquez-Fernández, H.S. Young, J.R. Requena & H. Wille. 2017. Early Stage Protein Misfolding and Amyloid Aggregation. Early Stage Protein Misfolding and Amyloid Aggregation 277 301 .
L. Breydo, J.M. Redington & V.N. Uversky. 2017. Early Stage Protein Misfolding and Amyloid Aggregation. Early Stage Protein Misfolding and Amyloid Aggregation 145 185 .
Vladislav Victorovich Khrustalev, Tatyana Aleksandrovna Khrustaleva, Kamil Szpotkowski, Victor Vitoldovich Poboinev & Katsiaryna Yurieuna Kakhanouskaya. (2016) The part of a long beta hairpin from the scrapie form of the human prion protein is reconstructed in the synthetic CC36 protein. Proteins: Structure, Function, and Bioinformatics 84:10, pages 1462-1479.
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S. Alexis Paz & Cameron F. Abrams. (2015) Free Energy and Hidden Barriers of the β-Sheet Structure of Prion Protein. Journal of Chemical Theory and Computation 11:10, pages 5024-5034.
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Martin L Daus. (2015) Techniques to elucidate the conformation of prions. World Journal of Biological Chemistry 6:3, pages 218.
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Paola Cavaliere, Joan Torrent, Stephanie Prigent, Vincenzo Granata, Kris Pauwels, Annalisa Pastore, Human Rezaei & Adriana Zagari. (2013) Binding of methylene blue to a surface cleft inhibits the oligomerization and fibrillization of prion protein. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1832:1, pages 20-28.
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Gianfranco Puoti, Alberto Bizzi, Gianluigi Forloni, Jiri G Safar, Fabrizio Tagliavini & Pierluigi Gambetti. (2012) Sporadic human prion diseases: molecular insights and diagnosis. The Lancet Neurology 11:7, pages 618-628.
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Khalid Salamat, Mohammed Moudjou, Jérôme Chapuis, Laetitia Herzog, Emilie Jaumain, Vincent Béringue, Human Rezaei, Annalisa Pastore, Hubert Laude & Michel Dron. (2012) Integrity of Helix 2-Helix 3 Domain of the PrP Protein Is Not Mandatory for Prion Replication. Journal of Biological Chemistry 287:23, pages 18953-18964.
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