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Commentary & View

The peculiar interaction between mammalian prion protein and RNA

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Pages 64-66 | Received 31 Jul 2008, Accepted 11 Sep 2008, Published online: 01 Oct 2008

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Indulekha P. Sudhakaran & Mani Ramaswami. (2017) Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains. RNA Biology 14:5, pages 568-586.
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Articles from other publishers (22)

Aishwarya AgarwalSandeep K. Rai, Anamika Avni & Samrat Mukhopadhyay. (2021) An intrinsically disordered pathological prion variant Y145Stop converts into self-seeding amyloids via liquid–liquid phase separation. Proceedings of the National Academy of Sciences 118:45.
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Richard Lathe & Jean-Luc Darlix. (2020) Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy. Archives of Virology 165:3, pages 535-556.
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Petar Stefanov Kovachev, Mariana P. B. Gomes, Yraima Cordeiro, Natália C. Ferreira, Leticia P. Felix Valadão, Lucas M. Ascari, Luciana P. Rangel, Jerson L. Silva & Suparna Sanyal. (2019) RNA modulates aggregation of the recombinant mammalian prion protein by direct interaction. Scientific Reports 9:1.
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Richard Lathe & Jean-Luc Darlix. (2017) Prion Protein PRNP: A New Player in Innate Immunity? The Aβ Connection. Journal of Alzheimer's Disease Reports 1:1, pages 263-275.
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Bruno Macedo, Ricardo Sant?Anna, Susanna Navarro, Yraima Cordeiro & Salvador Ventura. (2015) Mammalian prion protein (PrP) forms conformationally different amyloid intracellular aggregates in bacteria. Microbial Cell Factories 14:1.
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Hakkim Vovusha, Debapriya Banerjee, Nassima Oumata, Biplab Sanyal & Suparna Sanyal. (2015) Electronic structure and spectroscopic properties of 6-aminophenanthridine and its derivatives: Insights from density functional theory. International Journal of Quantum Chemistry 115:13, pages 846-852.
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Giuseppe Di Natale, Ildikó Turi, Giuseppe Pappalardo, Imre Sóvágó & Enrico Rizzarelli. (2015) Cross‐Talk Between the Octarepeat Domain and the Fifth Binding Site of Prion Protein Driven by the Interaction of Copper(II) with the N‐terminus. Chemistry – A European Journal 21:10, pages 4071-4084.
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Debapriya Banerjee & Suparna Sanyal. (2014) Protein Folding Activity of the Ribosome (PFAR) –– A Target for Antiprion Compounds. Viruses 6:10, pages 3907-3924.
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Juliana A. P. Chaves, Carolina Sanchez-López, Mariana P. B. Gomes, Tháyna Sisnande, Bruno Macedo, Vanessa End de Oliveira, Carolina A. C. Braga, Luciana P. Rangel, Jerson L. Silva, Liliana Quintanar & Yraima Cordeiro. (2014) Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids. JBIC Journal of Biological Inorganic Chemistry 19:6, pages 839-851.
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Yraima Cordeiro, Bruno Macedo, Jerson L. Silva & Mariana P. B. Gomes. (2014) Pathological implications of nucleic acid interactions with proteins associated with neurodegenerative diseases. Biophysical Reviews 6:1, pages 97-110.
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Shinji Higashi, Tomohiro Kabuta, Yoshitaka Nagai, Yukihiro Tsuchiya, Haruhiko Akiyama & Keiji Wada. (2013) TDP-43 associates with stalled ribosomes and contributes to cell survival during cellular stress. Journal of Neurochemistry 126:2, pages 288-300.
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Mark J. Millan. (2013) An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy. Neuropharmacology 68, pages 2-82.
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Liliana Malinovska, Sonja Kroschwald & Simon Alberti. (2013) Protein disorder, prion propensities, and self-organizing macromolecular collectives. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics 1834:5, pages 918-931.
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Ana P.D. Ano Bom, Luciana P. Rangel, Danielly C.F. Costa, Guilherme A.P. de Oliveira, Daniel Sanches, Carolina A. Braga, Lisandra M. Gava, Carlos H.I. Ramos, Ana O.T. Cepeda, Ana C. Stumbo, Claudia V. De Moura Gallo, Yraima Cordeiro & Jerson L. Silva. (2012) Mutant p53 Aggregates into Prion-like Amyloid Oligomers and Fibrils. Journal of Biological Chemistry 287:33, pages 28152-28162.
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Mariana P. B. Gomes, Tuane C. R. G. Vieira, Yraima Cordeiro & Jerson L. Silva. (2012) The role of RNA in mammalian prion protein conversion. Wiley Interdisciplinary Reviews: RNA 3:3, pages 415-428.
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Sandrine Alais, Ricardo Soto-Rifo, Vincent Balter, Henri Gruffat, Evelyne Manet, Laurent Schaeffer, Jean Luc Darlix, Andrea Cimarelli, Gra?a Raposo, Th?ophile Ohlmann & Pascal Leblanc. (2011) Functional mechanisms of the cellular prion protein (PrPC) associated anti-HIV-1 properties. Cellular and Molecular Life Sciences 69:8, pages 1331-1352.
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Rodrigo Diaz-Espinoza, Abhisek Mukherjee & Claudio Soto. (2012) Kosmotropic Anions Promote Conversion of Recombinant Prion Protein into a PrPSc-Like Misfolded Form. PLoS ONE 7:2, pages e31678.
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Cécile Guichard, Roland Ivanyi-Nagy, Kamal Kant Sharma, Caroline Gabus, Daniel Marc, Yves Mély & Jean-Luc Darlix. (2011) Analysis of nucleic acid chaperoning by the prion protein and its inhibition by oligonucleotides. Nucleic Acids Research 39:19, pages 8544-8558.
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Douglas J. Martin & Marina Ramirez-Alvarado. (2011) Glycosaminoglycans promote fibril formation by amyloidogenic immunoglobulin light chains through a transient interaction. Biophysical Chemistry 158:1, pages 81-89.
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Jerson L. Silva, Tuane C.R.G. Vieira, Mariana P.B. Gomes, Luciana P. Rangel, Sandra M.N. Scapin & Yraima Cordeiro. (2011) Experimental approaches to the interaction of the prion protein with nucleic acids and glycosaminoglycans: Modulators of the pathogenic conversion. Methods 53:3, pages 306-317.
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Hailing Jin & Jian-Kang Zhu. (2010) A viral suppressor protein inhibits host RNA silencing by hooking up with Argonautes: Figure 1.. Genes & Development 24:9, pages 853-856.
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Annette Eva Langkilde & Bente Vestergaard. (2009) Methods for structural characterization of prefibrillar intermediates and amyloid fibrils. FEBS Letters 583:16, pages 2600-2609.
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