Scavenger, transducer, RNA chaperone? What ligands of the prion protein teach us about its function
暂无分享,去创建一个
D. Marc | D. Marc | R. Mercey | F. Lantier | F. Lantier | R. Mercey
[1] S. Prusiner,et al. Trafficking of prion proteins through a caveolae-mediated endosomal pathway , 2003, The Journal of cell biology.
[2] H. Dyson,et al. Intrinsically unstructured proteins and their functions , 2005, Nature Reviews Molecular Cell Biology.
[3] G. Friedlander,et al. Characterization of Detergent-insoluble Complexes Containing the Cellular Prion Protein and Its Scrapie Isoform* , 1997, The Journal of Biological Chemistry.
[4] V. Mutel,et al. NADPH oxidase and extracellular regulated kinases 1/2 are targets of prion protein signaling in neuronal and nonneuronal cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[5] D. Dormont,et al. Bovine prion is endocytosed by human enterocytes via the 37 kDa/67 kDa laminin receptor. , 2005, The American journal of pathology.
[6] James E. Cleaver,et al. Search for a Prion-Specific Nucleic Acid , 2005, Journal of Virology.
[7] G. Pielak,et al. FlgM gains structure in living cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[8] 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.
[9] F. Cohen,et al. Identification of the Cu2+ binding sites in the N-terminal domain of the prion protein by EPR and CD spectroscopy. , 2000, Biochemistry.
[10] H. Schätzl,et al. Essential Role of the Prion Protein N Terminus in Subcellular Trafficking and Half-life of Cellular Prion Protein* , 2003, The Journal of Biological Chemistry.
[11] F. Cohen,et al. Identification of Candidate Proteins Binding to Prion Protein , 1997, Neurobiology of Disease.
[12] Gildon Choi,et al. Structural insights into the interaction between prion protein and nucleic acid. , 2006, Biochemistry.
[13] P. Schürmann,et al. Evidence of Presynaptic Location and Function of the Prion Protein , 1999, The Journal of Neuroscience.
[14] S. Lehmann. [The prion protein]. , 2002, Journal de la Societe de biologie.
[15] Peter Tompa,et al. The role of structural disorder in the function of RNA and protein chaperones , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] Witold K. Surewicz,et al. Crystal structure of the human prion protein reveals a mechanism for oligomerization , 2002, Nature Structural Biology.
[17] A. Mangé,et al. PrP‐dependent cell adhesion in N2a neuroblastoma cells , 2002, FEBS letters.
[18] J. Collinge,et al. A reassessment of copper(II) binding in the full-length prion protein. , 2006, The Biochemical journal.
[19] H. Kretzschmar,et al. Prion protein induced signaling cascades in monocytes. , 2006, Biochemical and biophysical research communications.
[20] A. Giese,et al. Mouse brain synaptosomes accumulate copper-67 efficiently by two distinct processes independent of cellular prion protein , 2007, Journal of Molecular Neuroscience.
[21] Eckart D Gundelfinger,et al. An Architectural Framework That May Lie at the Core of the Postsynaptic Density , 2006, Science.
[22] F. Cohen,et al. Synthetic Mammalian Prions , 2004, Science.
[23] N. Hooper,et al. Assigning functions to distinct regions of the N-terminus of the prion protein that are involved in its copper-stimulated, clathrin-dependent endocytosis , 2005, Journal of Cell Science.
[24] Marc S. Cortese,et al. Flexible nets , 2005, The FEBS journal.
[25] D. Dormont,et al. The 37‐kDa/67‐kDa laminin receptor acts as the cell‐surface receptor for the cellular prion protein , 2001, The EMBO journal.
[26] Benjamin A. Shoemaker,et al. Speeding molecular recognition by using the folding funnel: the fly-casting mechanism. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[27] D. Harris,et al. Copper Stimulates Endocytosis of the Prion Protein* , 1998, The Journal of Biological Chemistry.
[28] A. Mangé,et al. Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin , 2004, Journal of Cell Science.
[29] Stanley B. Prusiner,et al. The Priori Diseases , 1998 .
[30] J. Cechetto,et al. Localization of Mitochondrial 60-kD Heat Shock Chaperonin Protein (Hsp60) in Pituitary Growth Hormone Secretory Granules and Pancreatic Zymogen Granules , 2000, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[31] R. Cohn. Dystroglycan: important player in skeletal muscle and beyond , 2005, Neuromuscular Disorders.
[32] G. J. Raymond,et al. Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells , 1993, Journal of virology.
[33] S. Prusiner,et al. Nucleic acids in prion preparations: unspecific background or essential component? , 1994, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[34] R. Cousins,et al. Mammalian zinc transporters. , 1998, Annual review of nutrition.
[35] J. Weber,et al. Similar Turnover and Shedding of the Cellular Prion Protein in Primary Lymphoid and Neuronal Cells* , 2001, The Journal of Biological Chemistry.
[36] D. Westaway,et al. The Expanding Universe of Prion Diseases , 2006, PLoS pathogens.
[37] N. Cashman,et al. Nearly ubiquitous tissue distribution of the scrapie agent precursor protein , 1992, Neurology.
[38] A Keith Dunker,et al. Conservation of intrinsic disorder in protein domains and families: II. functions of conserved disorder. , 2006, Journal of proteome research.
[39] S. Haswell,et al. Normal prion protein has an activity like that of superoxide dismutase. , 1999, The Biochemical journal.
[40] C. Weissmann. Birth of a Prion: Spontaneous Generation Revisited , 2005, Cell.
[41] A. Palsdottir,et al. Interaction of PrP with NRAGE, a protein involved in neuronal apoptosis , 2005, Molecular and Cellular Neuroscience.
[42] L. Hood,et al. Identification of cellular proteins binding to the scrapie prion protein. , 1990, Biochemistry.
[43] S. Prusiner,et al. Cooperative binding of dominant-negative prion protein to kringle domains. , 2003, Journal of molecular biology.
[44] S. Prusiner,et al. Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein. , 1990, Biochemistry.
[45] Y. Cordeiro,et al. DNA Converts Cellular Prion Protein into the β-Sheet Conformation and Inhibits Prion Peptide Aggregation* , 2001, The Journal of Biological Chemistry.
[46] Markus Glatzel,et al. Plasminogen binds to disease-associated prion protein of multiple species , 2001, The Lancet.
[47] J. Turnbull,et al. Identification of the Heparan Sulfate Binding Sites in the Cellular Prion Protein* , 2002, The Journal of Biological Chemistry.
[48] M. Famulok,et al. Prion‐Protein‐Specific Aptamer Reduces PrPSc Formation , 2002, Chembiochem : a European journal of chemical biology.
[49] C. Kurschner,et al. The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system. , 1995, Brain research. Molecular brain research.
[50] P. Greengard,et al. Specificity of the Binding of Synapsin I to Src Homology 3 Domains* , 2000, The Journal of Biological Chemistry.
[51] L. Pinna,et al. Bovine prion protein as a modulator of protein kinase CK2. , 2000, The Biochemical journal.
[52] S. Haswell,et al. Consequences of manganese replacement of copper for prion protein function and proteinase resistance , 2000, The EMBO journal.
[53] Ping Wang,et al. DNA Aptamers That Bind to PrPC and Not PrpSc Show Sequence and Structure Specificity , 2006, Experimental biology and medicine.
[54] J. Fournier,et al. Nonneuronal cellular prion protein. , 2001, International review of cytology.
[55] Alexander V. Gourine,et al. ATP is a mediator of chemosensory transduction in the central nervous system , 2005, Nature.
[56] S. Prusiner,et al. Determinants of carboxyl-terminal domain translocation during prion protein biogenesis. , 1994, The Journal of biological chemistry.
[57] J. Gitlin,et al. Copper homeostasis in the CNS , 2006, Molecular Neurobiology.
[58] F. Castellino,et al. The kringle domains of human plasminogen. , 1997, Ciba Foundation symposium.
[59] R. Riek. NMR structure of the mouse prion protein , 1998 .
[60] D. Harris,et al. Copper and zinc cause delivery of the prion protein from the plasma membrane to a subset of early endosomes and the Golgi , 2003, Journal of neurochemistry.
[61] S. Prusiner,et al. Identification of a protein that purifies with the scrapie prion. , 1982, Science.
[62] L. Hood,et al. Scrapie and cellular prion proteins share polypeptide epitopes. , 1986, The Journal of infectious diseases.
[63] S. Prusiner,et al. Cytosolic Prion Protein in Neurons , 2003, The Journal of Neuroscience.
[64] S. Prusiner,et al. Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor. , 1993, Glycobiology.
[65] C. Zurzolo,et al. The highways and byways of prion protein trafficking. , 2005, Trends in cell biology.
[66] M. Gravenor,et al. Investigation of trace elements in soil as risk factors in the epidemiology of scrapie , 2004, Veterinary Record.
[67] W. Surewicz,et al. Membrane Environment Alters the Conformational Structure of the Recombinant Human Prion Protein* , 1999, The Journal of Biological Chemistry.
[68] S. Prusiner. Novel proteinaceous infectious particles cause scrapie. , 1982, Science.
[69] R. S. Stewart,et al. Cytosolic Prion Protein (PrP) Is Not Toxic in N2a Cells and Primary Neurons Expressing Pathogenic PrP Mutations* , 2005, Journal of Biological Chemistry.
[70] Zoran Obradovic,et al. The protein trinity—linking function and disorder , 2001, Nature Biotechnology.
[71] N. Hooper,et al. The prion protein and neuronal zinc homeostasis. , 2003, Trends in biochemical sciences.
[72] K. Hsiao,et al. Neurotoxicity of the prion protein , 1994, Neurobiology of Aging.
[73] J. Launay,et al. Modulation of Serotonergic Receptor Signaling and Cross-talk by Prion Protein* , 2005, Journal of Biological Chemistry.
[74] W. James,et al. Structural Determinants of Conformationally Selective, Prion-binding Aptamers*[boxs] , 2004, Journal of Biological Chemistry.
[75] J. Laplanche,et al. Signal transduction through prion protein. , 2000, Science.
[76] P. Tompa. Intrinsically unstructured proteins evolve by repeat expansion , 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.
[77] N. Vassallo,et al. Cellular prion protein function in copper homeostasis and redox signalling at the synapse , 2003, Journal of neurochemistry.
[78] K. Tew,et al. Trace elements in human physiology and pathology: zinc and metallothioneins. , 2003, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[79] S. Prusiner,et al. Biogenesis and Transmembrane Orientation of the Cellular Isoform of the Scrapie Prion Protein , 1987, Molecular and cellular biology.
[80] D. Westaway,et al. The cellular prion protein binds copper in vivo , 1997, Nature.
[81] A. Strom,et al. Identification of prion protein binding proteins by combined use of far‐Western immunoblotting, two dimensional gel electrophoresis and mass spectrometry , 2006, Proteomics.
[82] K. Lee,et al. Endocytic Intermediates Involved with the Intracellular Trafficking of a Fluorescent Cellular Prion Protein* , 2002, The Journal of Biological Chemistry.
[83] J. Rossier,et al. Cellular prion protein/laminin receptor: distribution in adult central nervous system and characterization of an isoform associated with a subtype of cortical neurons , 2004, The European journal of neuroscience.
[84] D. Harris,et al. Cell Surface Expression of the Prion Protein in Yeast Does Not Alter Copper Utilization Phenotypes* , 2004, Journal of Biological Chemistry.
[85] H. Schätzl,et al. PrPC Directly Interacts with Proteins Involved in Signaling Pathways* , 2001, The Journal of Biological Chemistry.
[86] L. Davidovic,et al. Disordered RNA chaperone proteins: from functions to disease , 2005, Cellular and Molecular Life Sciences CMLS.
[87] G. Hutter,et al. No Superoxide Dismutase Activity of Cellular Prion Protein in vivo , 2003, Biological chemistry.
[88] S. Katamine,et al. PrP fragment 106‐126 is toxic to cerebral endothelial cells expressing PrPC , 2000, Neuroreport.
[89] M. Schachner,et al. Prion protein as trans-interacting partner for neurons is involved in neurite outgrowth and neuronal survival , 2003, Molecular and Cellular Neuroscience.
[90] S. Itohara,et al. PrP cooperates with STI1 to regulate SOD activity in PrP-deficient neuronal cell line. , 2005, Biochemical and biophysical research communications.
[91] Adriano Aguzzi,et al. Binding of disease-associated prion protein to plasminogen , 2000, Nature.
[92] S. Prusiner,et al. Human prions and plasma lipoproteins. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[93] J. C. Wilkinson,et al. XIAP Is a copper binding protein deregulated in Wilson's disease and other copper toxicosis disorders. , 2006, Molecular cell.
[94] Peter Critchley,et al. Binding of prion proteins to lipid membranes. , 2004, Biochemical and biophysical research communications.
[95] J. Lakey,et al. Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides. , 1995, Biochemical and biophysical research communications.
[96] R. Pogni,et al. Interaction of the human prion PrP(106-126) sequence with copper(II), manganese(II), and zinc(II): NMR and EPR studies. , 2005, Journal of the American Chemical Society.
[97] J. Hope,et al. Characterization of 2′-Fluoro-RNA Aptamers That Bind Preferentially to Disease-associated Conformations of Prion Protein and Inhibit Conversion* , 2003, Journal of Biological Chemistry.
[98] G. Forloni,et al. Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Sträussler-Scheinker disease peptides in the presence of metal ions. , 2006, Biochemistry.
[99] David R. Brown,et al. High Affinity Binding between Copper and Full-length Prion Protein Identified by Two Different Techniques* , 2005, Journal of Biological Chemistry.
[100] Andrea Barta,et al. Strategies for RNA folding and assembly , 2004, Nature Reviews Molecular Cell Biology.
[101] J. H. Viles,et al. Copper Binding to the Octarepeats of the Prion Protein , 2003, The Journal of Biological Chemistry.
[102] M. Sy,et al. Cell-surface prion protein interacts with glycosaminoglycans. , 2002, The Biochemical journal.
[103] R. Brentani,et al. Complementary hydropathy identifies a cellular prion protein receptor , 1997, Nature Medicine.
[104] J. Fournier,et al. The cellular prion protein: A new partner of the lectin CBP70 in the nucleus of NB4 human promyelocytic leukemia cells * , 2002, Journal of cellular biochemistry.
[105] J. Grosclaude,et al. Sequential generation of two structurally distinct ovine prion protein soluble oligomers displaying different biochemical reactivities. , 2005, Journal of molecular biology.
[106] T. Bartke,et al. Association of Bcl-2 with misfolded prion protein is linked to the toxic potential of cytosolic PrP. , 2006, Molecular biology of the cell.
[107] B. Caughey,et al. Potent Antiscrapie Activities of Degenerate Phosphorothioate Oligonucleotides , 2006, Antimicrobial Agents and Chemotherapy.
[108] R. S. Stewart,et al. A Transmembrane Form of the Prion Protein Is Localized in the Golgi Apparatus of Neurons* , 2005, Journal of Biological Chemistry.
[109] Arunandan Kumar,et al. The Chaperone Protein BiP Binds to a Mutant Prion Protein and Mediates Its Degradation by the Proteasome* , 2000, The Journal of Biological Chemistry.
[110] S. Prusiner,et al. Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells , 1990, The Journal of cell biology.
[111] A. Giese,et al. Effect of metal ions on de novo aggregation of full-length prion protein. , 2004, Biochemical and biophysical research communications.
[112] A. Verkman,et al. Biogenesis and transmembrane topology of the CHIP28 water channel at the endoplasmic reticulum , 1994, The Journal of cell biology.
[113] A. Burlingame,et al. Stress‐inducible protein 1 is a cell surface ligand for cellular prion that triggers neuroprotection , 2002, The EMBO journal.
[114] Samarjit Bhattacharyya,et al. Internalization and recycling of 5-HT2A receptors activated by serotonin and protein kinase C-mediated mechanisms , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[115] J. Satoh,et al. The 14-3-3 Protein Forms a Molecular Complex with Heat Shock Protein Hsp60 and Cellular Prion Protein , 2005, Journal of neuropathology and experimental neurology.
[116] S. Lindquist,et al. Neurotoxicity and Neurodegeneration When PrP Accumulates in the Cytosol , 2002, Science.
[117] Tae-Joon Jeon,et al. Transmembrane glycine zippers: physiological and pathological roles in membrane proteins. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[118] Shu G. Chen,et al. Aberrant metal binding by prion protein in human prion disease , 2001, Journal of neurochemistry.
[119] R. Gabizon,et al. The Cellular Prion Protein Colocalizes with the Dystroglycan Complex in the Brain , 2000, Journal of neurochemistry.
[120] 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.
[121] Y. Shaked,et al. The binding of prion proteins to serum components is affected by detergent extraction conditions , 2002, Journal of neurochemistry.
[122] M. Famulok,et al. RNA aptamers specifically interact with the prion protein PrP , 1997, Journal of virology.
[123] D. Harris. Trafficking, turnover and membrane topology of PrP. , 2003, British medical bulletin.
[124] T. Gibson,et al. Systematic Discovery of New Recognition Peptides Mediating Protein Interaction Networks , 2005, PLoS biology.
[125] C. Gabus,et al. PrPC has nucleic acid chaperoning properties similar to the nucleocapsid protein of HIV-1. , 2002, Comptes rendus biologies.
[126] Ralph Zahn,et al. The octapeptide repeats in mammalian prion protein constitute a pH-dependent folding and aggregation site. , 2003, Journal of molecular biology.
[127] M. Angeletti,et al. Binding of recombinant PrPc to human plasminogen: Kinetic and thermodynamic study using a resonant mirror biosensor , 2004, Proteins.
[128] C. Sunyach,et al. The mechanism of internalization of glycosylphosphatidylinositol‐anchored prion protein , 2003, The EMBO journal.
[129] J. Collinge,et al. Location and properties of metal-binding sites on the human prion protein , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[130] M. Famulok,et al. Prion protein PrPc interacts with molecular chaperones of the Hsp60 family , 1996, Journal of virology.
[131] M. Gasset,et al. Prion protein interaction with glycosaminoglycan occurs with the formation of oligomeric complexes stabilized by Cu(II) bridges. , 2002, Journal of molecular biology.
[132] P. D. Nagy,et al. Characterization of the RNA-Binding Domains in the Replicase Proteins of Tomato Bushy Stunt Virus , 2003, Journal of Virology.
[133] H. Kretzschmar,et al. Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survival. , 2005, Biochemical and biophysical research communications.
[134] P. Nandi,et al. Murine recombinant prion protein induces ordered aggregation of linear nucleic acids to condensed globular structures , 2001, Archives of Virology.
[135] R. Linden,et al. Cellular prion protein transduces neuroprotective signals , 2002, The EMBO journal.
[136] David A Agard,et al. Structural studies of the scrapie prion protein by electron crystallography , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[137] F. Cohen,et al. Time-controlled transcardiac perfusion cross-linking for the study of protein interactions in complex tissues , 2004, Nature Biotechnology.
[138] R. Tsenkova,et al. Prion protein fate governed by metal binding. , 2004, Biochemical and biophysical research communications.
[139] G. Forloni,et al. Neurotoxicity of a prion protein fragment , 1993, Nature.
[140] N. Loberto,et al. The membrane environment of endogenous cellular prion protein in primary rat cerebellar neurons , 2005, Journal of neurochemistry.
[141] David R. Brown. Role of the prion protein in copper turnover in astrocytes , 2004, Neurobiology of Disease.
[142] S. Haswell,et al. Antioxidant activity related to copper binding of native prion protein , 2001, Journal of neurochemistry.
[143] K Wüthrich,et al. NMR characterization of the full‐length recombinant murine prion protein, mPrP(23–231) , 1997, FEBS letters.
[144] A. Favier,et al. Expression of Prion Protein Increases Cellular Copper Binding and Antioxidant Enzyme Activities but Not Copper Delivery* , 2003, The Journal of Biological Chemistry.
[145] D. Engelman,et al. Translocation of molecules into cells by pH-dependent insertion of a transmembrane helix. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[146] Christopher E. Jones,et al. Probing copper2+ binding to the prion protein using diamagnetic nickel2+ and 1H NMR: the unstructured N terminus facilitates the coordination of six copper2+ ions at physiological concentrations. , 2005, Journal of molecular biology.
[147] Terrance T. Kummer,et al. Mutant Prion Proteins Are Partially Retained in the Endoplasmic Reticulum* , 2001, The Journal of Biological Chemistry.
[148] S. Haswell,et al. Metal imbalance and compromised antioxidant function are early changes in prion disease. , 2002, The Biochemical journal.
[149] S. Prusiner,et al. A transmembrane form of the prion protein in neurodegenerative disease. , 1998, Science.
[150] J. Grassi,et al. Immunolocalization of the cellular prion protein in normal brain , 2000, Microscopy research and technique.
[151] C. Sigurdson,et al. [Prion diseases?]. , 1985, Deutsche medizinische Wochenschrift.
[152] J. Collinge,et al. Transmission of Scrapie by Steel-surface-bound Prions , 2001, Molecular medicine.
[153] S. Itohara,et al. Prions prevent neuronal cell-line death , 1999, Nature.
[154] C. Bostock,et al. Characterization and polyanion-binding properties of purified recombinant prion protein. , 1999, The Biochemical journal.
[155] D. Dormont,et al. Identification of interaction domains of the prion protein with its 37‐kDa/67‐kDa laminin receptor , 2001, The EMBO journal.
[156] Fred E. Cohen,et al. Evidence for assembly of prions with left-handed β-helices into trimers , 2004 .
[157] J. Vincent,et al. In Vivo Cytotoxicity of the Prion Protein Fragment 106–126* , 2000, The Journal of Biological Chemistry.
[158] J. Collinge,et al. Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4. , 2006, The Biochemical journal.
[159] S. Basu,et al. Cell-Specific Metabolism and Pathogenesis of Transmembrane Prion Protein , 2006, Molecular and Cellular Biology.
[160] A. Giese,et al. Function of PrP(C) as a copper-binding protein at the synapse. , 2000, Archives of virology. Supplementum.
[161] A. Bush,et al. The neurobiology of zinc in health and disease , 2005, Nature Reviews Neuroscience.
[162] R. Murali,et al. The hidden code in genomics: a tool for gene discovery , 2001, Journal of molecular recognition : JMR.
[163] F. Cohen,et al. Evidence for assembly of prions with left-handed beta-helices into trimers. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[164] J. Collinge,et al. Strain-specific prion-protein conformation determined by metal ions , 1999, Nature Cell Biology.
[165] J. Power,et al. Copper and Zinc , 1997 .
[166] H. Takeuchi,et al. Copper reduction by the octapeptide repeat region of prion protein: pH dependence and implications in cellular copper uptake. , 2005, Biochemistry.
[167] J. Collinge,et al. Recombinant prion protein does not possess SOD-1 activity. , 2005, The Biochemical journal.
[168] S. Prusiner,et al. Unusual topogenic sequence directs prion protein biogenesis. , 1990, Science.
[169] I. Izquierdo,et al. Cellular prion protein binds laminin and mediates neuritogenesis. , 2000, Brain research. Molecular brain research.
[170] H. Diringer,et al. Dextran sulphate 500 delays and prevents mouse scrapie by impairment of agent replication in spleen. , 1984, The Journal of general virology.
[171] G. Edelman,et al. Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein. , 2001, Journal of molecular biology.
[172] F. Edenhofer,et al. The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells , 1997, Nature Medicine.
[173] F. Cohen,et al. Prion protein selectively binds copper(II) ions. , 1998, Biochemistry.
[174] Judit Ovádi,et al. On the origin of intracellular compartmentation and organized metabolic systems , 2004, Molecular and Cellular Biochemistry.
[175] P. Nandi. Interaction of prion peptide HuPrP106–126 with nucleic acid , 1997, Archives of Virology.
[176] J. Grosclaude,et al. Fast, reversible interaction of prion protein with RNA aptamers containing specific sequence patterns , 2006, Archives of Virology.
[177] S. Supattapone,et al. RNA molecules stimulate prion protein conversion , 2003, Nature.