The prion protein binds thiamine
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Li Li | Ying W. Dong | David Hau | D. Hau | T. Bjorndahl | R. Perez-Pineiro | N. Cashman | C. Ladner | M. Berjanskii | Rolando Perez‐Pineiro | Trent C. Bjorndahl | Mark V. Berjanskii | Alan Huang | Rose Lee | Ebrima Gibbs | Carol Ladner | Ying Wei Dong | Ashenafi Abera | Neil R. Cashman | David S. Wishart | D. Wishart | E. Gibbs | Li Li | Alan Huang | Rose Lee | Ashenafi Abera
[1] Eric Oldfield,et al. 1H, 13C and 15N chemical shift referencing in biomolecular NMR , 1995, Journal of biomolecular NMR.
[2] S. Grzesiek,et al. NMRPipe: A multidimensional spectral processing system based on UNIX pipes , 1995, Journal of biomolecular NMR.
[3] S. Hornemann,et al. Prion protein NMR structure from tammar wallaby (Macropus eugenii) shows that the beta2-alpha2 loop is modulated by long-range sequence effects. , 2009, Journal of molecular biology.
[4] U. Agrimi,et al. Advances in scrapie research. , 2007, Revue scientifique et technique.
[5] Charles D Schwieters,et al. The Xplor-NIH NMR molecular structure determination package. , 2003, Journal of magnetic resonance.
[6] M. Moudjou,et al. Cellular prion protein status in sheep: tissue-specific biochemical signatures. , 2001, The Journal of general virology.
[7] Frank Baumann,et al. Axonal prion protein is required for peripheral myelin maintenance , 2010, Nature Neuroscience.
[8] Egon L. Willighagen,et al. The Blue Obelisk—Interoperability in Chemical Informatics , 2006, J. Chem. Inf. Model..
[9] David S. Goodsell,et al. AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility , 2009, J. Comput. Chem..
[10] L. Schonberger,et al. Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. , 2002, Clinics in laboratory medicine.
[11] J. Berger. Kuru in the 21st century—an acquired human prion disease with very long incubation periods , 2008 .
[12] D. Harris,et al. The cellular prion protein (PrP(C)): its physiological function and role in disease. , 2007, Biochimica et biophysica acta.
[13] D. Westaway,et al. The prion protein family: diversity, rivalry, and dysfunction. , 2007, Biochimica et biophysica acta.
[14] Constance A. Sobsey,et al. Detailed biophysical characterization of the acid-induced PrP(c) to PrP(β) conversion process. , 2011, Biochemistry.
[15] Stanley B. Prusiner,et al. Nobel Lecture: Prions , 1998 .
[16] D S Goodsell,et al. Automated docking of flexible ligands: Applications of autodock , 1996, Journal of molecular recognition : JMR.
[17] F. Cohen,et al. Cryptic epitopes in N‐terminally truncated prion protein are exposed in the full‐length molecule: Dependence of conformation on pH , 2001, Proteins.
[18] F. Chantraine,et al. Thiamine Status in Humans and Content of Phosphorylated Thiamine Derivatives in Biopsies and Cultured Cells , 2010, PloS one.
[19] 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.
[20] Bruce A Johnson,et al. Using NMRView to visualize and analyze the NMR spectra of macromolecules. , 2004, Methods in molecular biology.
[21] D. Lütjohann,et al. Simvastatin prolongs survival times in prion infections of the central nervous system. , 2006, Biochemical and biophysical research communications.
[22] Iva Hafner-Bratkovič,et al. Curcumin binds to the α‐helical intermediate and to the amyloid form of prion protein – a new mechanism for the inhibition of PrPSc accumulation , 2008 .
[23] J. Collinge,et al. Pharmacological chaperone for the structured domain of human prion protein , 2010, Proceedings of the National Academy of Sciences.
[24] G. Forloni,et al. Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro. , 2000, Journal of molecular biology.
[25] G. J. Raymond,et al. Hemin Interactions and Alterations of the Subcellular Localization of Prion Protein* , 2007, Journal of Biological Chemistry.
[26] E. Walter,et al. The affinity of copper binding to the prion protein octarepeat domain: evidence for negative cooperativity. , 2006, Biochemistry.
[27] D. Lonsdale. A Review of the Biochemistry, Metabolism and Clinical Benefits of Thiamin(e) and Its Derivatives , 2006, Evidence-based complementary and alternative medicine : eCAM.
[28] K. Jellinger,et al. Fatal familial insomnia: a new Austrian family. , 1999, Brain : a journal of neurology.
[29] B. Meyer,et al. Group epitope mapping by saturation transfer difference NMR to identify segments of a ligand in direct contact with a protein receptor. , 2001, Journal of the American Chemical Society.
[30] F E Cohen,et al. Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[31] K. Fiebig,et al. Antimalarial drug quinacrine binds to C-terminal helix of cellular prion protein. , 2003, Journal of medicinal chemistry.
[32] X. Xi,et al. Thermodynamic analysis of fluorescence enhancement and Quenching theory equations , 2008 .
[33] B. Caughey,et al. Prions and their partners in crime , 2006, Nature.
[34] V. Barone,et al. Assessing the acid–base and conformational properties of histidine residues in human prion protein (125–228) by means of pKa calculations and molecular dynamics simulations , 2006, Proteins.
[35] V. Ganapathy,et al. SLC19: the folate/thiamine transporter family , 2004, Pflügers Archiv.
[36] J. Lakowicz. Principles of fluorescence spectroscopy , 1983 .
[37] John Collinge,et al. Kuru in the 21st century—an acquired human prion disease with very long incubation periods , 2006, The Lancet.
[38] David S. Wishart,et al. HMDB: a knowledgebase for the human metabolome , 2008, Nucleic Acids Res..
[39] A. Schmidtchen,et al. Antimicrobial Activity of Human Prion Protein Is Mediated by Its N-Terminal Region , 2009, PloS one.
[40] M. Miller,et al. Chronic wasting disease of cervids. , 2004, Current topics in microbiology and immunology.
[41] M. Álvarez-Martínez,et al. Physiological role of the cellular prion protein. , 2008, Veterinary research.
[42] R. Davis,et al. Protein binding of thiamin in human plasma. , 1986, International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.
[43] Andrea Didier,et al. Tissue-specific expression pattern of bovine prion gene: quantification using real-time RT-PCR. , 2003, Molecular and cellular probes.
[44] S. V. Anisimov,et al. Congo red and protein aggregation in neurodegenerative diseases , 2007, Brain Research Reviews.