Prion protein conversion in vitro
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[1] B. Caughey,et al. A solid-phase assay for identification of modulators of prion protein interactions. , 2003, Analytical biochemistry.
[2] S. Supattapone,et al. RNA molecules stimulate prion protein conversion , 2003, Nature.
[3] J. Esko,et al. Cellular Heparan Sulfate Participates in the Metabolism of Prions* , 2003, Journal of Biological Chemistry.
[4] L. Stoltze,et al. A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[5] R. Rubenstein,et al. Small, highly structured RNAs participate in the conversion of human recombinant PrP(Sen) to PrP(Res) in vitro. , 2003, Journal of molecular biology.
[6] G. J. Raymond,et al. Inhibition of Protease-Resistant Prion Protein Accumulation In Vitro by Curcumin , 2003, Journal of Virology.
[7] S. Supattapone,et al. In vitro amplification of protease-resistant prion protein requires free sulfhydryl groups. , 2003, Biochemistry.
[8] V. Kryukov,et al. Concentration and removal of prion proteins from biological solutions , 2003, Biotechnology and applied biochemistry.
[9] Yaping Gu,et al. Identification of cryptic nuclear localization signals in the prion protein , 2003, Neurobiology of Disease.
[10] E. Cohen,et al. Scrapie‐like prion protein accumulates in aggresomes of cyclosporin A‐treated cells , 2003, The EMBO journal.
[11] S. Lindquist,et al. Conversion of PrP to a Self-Perpetuating PrPSc-like Conformation in the Cytosol , 2002, Science.
[12] P. Nandi,et al. DNA-induced partial unfolding of prion protein leads to its polymerisation to amyloid. , 2002, Journal of molecular biology.
[13] H. Scheraga,et al. Intramolecular Versus Intermolecular Disulfide Bonds in Prion Proteins* , 2002, The Journal of Biological Chemistry.
[14] M. Famulok,et al. Prion‐Protein‐Specific Aptamer Reduces PrPSc Formation , 2002, Chembiochem : a European journal of chemical biology.
[15] J. Wissler. Engineering of Capillary Patterns in Muscle by a Nonmitogenic Copper‐Ribonucleoprotein Angiomorphogen [Angiotropin CuRNP Ribokine] , 2002, Annals of the New York Academy of Sciences.
[16] J. Turnbull,et al. Identification of the Heparan Sulfate Binding Sites in the Cellular Prion Protein* , 2002, The Journal of Biological Chemistry.
[17] S. L. Le Grice,et al. Functional interactions of nucleocapsid protein of feline immunodeficiency virus and cellular prion protein with the viral RNA. , 2002, Journal of molecular biology.
[18] István Simon,et al. The role of dimerization in prion replication. , 2002, Biophysical journal.
[19] B. Chesebro,et al. Conversion of raft associated prion protein to the protease‐resistant state requires insertion of PrP‐res (PrPSc) into contiguous membranes , 2002, The EMBO journal.
[20] Craig P. Hunter,et al. Systemic RNAi in C. elegans Requires the Putative Transmembrane Protein SID-1 , 2002, Science.
[21] C. Gabus,et al. PrPC has nucleic acid chaperoning properties similar to the nucleocapsid protein of HIV-1. , 2002, Comptes rendus biologies.
[22] D. Dormont,et al. Identification of interaction domains of the prion protein with its 37‐kDa/67‐kDa laminin receptor , 2001, The EMBO journal.
[23] Albert Taraboulos,et al. Proteasomes and ubiquitin are involved in the turnover of the wild‐type prion protein , 2001, The EMBO journal.
[24] Y. Shaked,et al. A Protease-resistant Prion Protein Isoform Is Present in Urine of Animals and Humans Affected with Prion Diseases* , 2001, The Journal of Biological Chemistry.
[25] F. Hartl,et al. A sensitive filter retention assay for the detection of PrPSc and the screening of anti‐prion compounds , 2001 .
[26] B. Permanne,et al. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding , 2001, Nature.
[27] C. Gabus,et al. The Prion Protein Has RNA Binding and Chaperoning Properties Characteristic of Nucleocapsid Protein NCp7 of HIV-1* , 2001, The Journal of Biological Chemistry.
[28] Z. Meiner,et al. Reconstitution of Prion Infectivity from Solubilized Protease-resistant PrP and Nonprotein Components of Prion Rods* , 2001, The Journal of Biological Chemistry.
[29] C. Péchoux,et al. The prion protein has DNA strand transfer properties similar to retroviral nucleocapsid protein. , 2001, Journal of molecular biology.
[30] F. Cohen,et al. Branched Polyamines Cure Prion-Infected Neuroblastoma Cells , 2001, Journal of Virology.
[31] H. Scheraga,et al. A role for intermolecular disulfide bonds in prion diseases? , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[32] B. Chesebro,et al. Sulfated glycans and elevated temperature stimulate PrPSc‐dependent cell‐free formation of protease‐resistant prion protein , 2001, The EMBO journal.
[33] M. Feughelman,et al. Thiol-disulfide interchange a potential key to conformational change associated with amyloid fibril formation. , 2000, Journal of theoretical biology.
[34] B. Caughey,et al. Lysosomotropic Agents and Cysteine Protease Inhibitors Inhibit Scrapie-Associated Prion Protein Accumulation , 2000, Journal of virology.
[35] W. Caughey,et al. Porphyrin and phthalocyanine antiscrapie compounds. , 2000, Science.
[36] B. Chesebro,et al. Inhibition of formation of protease-resistant prion protein by Trypan Blue, Sirius Red and other Congo Red analogs. , 2000, Archives of virology. Supplementum.
[37] F. Cohen,et al. Quantitative traits of prion strains are enciphered in the conformation of the prion protein. , 2000, Archives of virology. Supplementum.
[38] F. Cohen,et al. Elimination of prions by branched polyamines and implications for therapeutics. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[39] J. Collinge,et al. Strain-specific prion-protein conformation determined by metal ions , 1999, Nature Cell Biology.
[40] J Collinge,et al. Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations. , 1999, Science.
[41] J. Aiken,et al. Reversibility of Scrapie Inactivation Is Enhanced by Copper* , 1998, The Journal of Biological Chemistry.
[42] F. Cohen,et al. Eight prion strains have PrPSc molecules with different conformations , 1998, Nature Medicine.
[43] B. Caughey,et al. The importance of the disulfide bond in prion protein conversion , 1998, Neuroreport.
[44] S. Prusiner,et al. A transmembrane form of the prion protein in neurodegenerative disease. , 1998, Science.
[45] M. Famulok,et al. RNA aptamers specifically interact with the prion protein PrP , 1997, Journal of virology.
[46] F E Cohen,et al. A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform. , 1997, Journal of molecular biology.
[47] P. Lansbury,et al. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans , 1997, Nature.
[48] G. J. Raymond,et al. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[49] F. Cohen,et al. Physical studies of conformational plasticity in a recombinant prion protein. , 1997, Biochemistry.
[50] S. Prusiner,et al. Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[51] F. Cohen,et al. High-level expression and characterization of a purified 142-residue polypeptide of the prion protein. , 1996, Biochemistry.
[52] S. Prusiner,et al. Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity , 1996, Journal of virology.
[53] P. Lansbury,et al. Non-genetic propagation of strain-specific properties of scrapie prion protein , 1995, Nature.
[54] P. Lansbury,et al. Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[55] R. Marsh,et al. Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy , 1994, Journal of virology.
[56] P. Lansbury,et al. Cell-free formation of protease-resistant prion protein , 1994, Nature.
[57] R J Fletterick,et al. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[58] P. Roller,et al. Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein. , 1993, The Journal of biological chemistry.
[59] S. Prusiner,et al. Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes , 1993, Cell.
[60] G. J. Raymond,et al. Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells , 1993, Journal of virology.
[61] R. Marsh,et al. Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent , 1992, Journal of virology.
[62] R. Marsh,et al. Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters. , 1992, The Journal of general virology.
[63] S. Prusiner,et al. Prion biology and diseases. , 1999, Harvey lectures.
[64] B. Caughey,et al. Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy. , 1991, Biochemistry.
[65] S. Prusiner,et al. Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins , 1990, Molecular and cellular biology.
[66] Stephen J. DeArmond,et al. Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques , 1989, Cell.
[67] L. Hood,et al. Purification and properties of the cellular and scrapie hamster prion proteins. , 1988, European journal of biochemistry.
[68] Stanley B. Prusiner,et al. Scrapie prion protein contains a phosphatidylinositol glycolipid , 1987, Cell.
[69] S. Prusiner,et al. Purified scrapie prions resist inactivation by procedures that hydrolyze, modify, or shear nucleic acids. , 1987, Virology.
[70] S. Prusiner,et al. Purified prion proteins and scrapie infectivity copartition into liposomes. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[71] S. Prusiner,et al. Separation and properties of cellular and scrapie prion proteins. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[72] S. Prusiner. Novel proteinaceous infectious particles cause scrapie. , 1982, Science.
[73] I. Pattison,et al. Modification of a strain of mouse-adapted scrapie by passage through rats. , 1968, Research in veterinary science.
[74] H. Fraser,et al. Identification of a gene which controls the incubation period of some strains of scrapie agent in mice. , 1968, Journal of comparative pathology.