| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0022-2836(02)00341-8 |
| P698 | PubMed publication ID | 12051926 |
| P50 | author | María Gasset | Q40216171 |
| Juan Carlos Espinosa | Q42538221 | ||
| María A. Pajares | Q42970312 | ||
| Carmen Ocal | Q50658536 | ||
| P2093 | author name string | Bruno Oesch | |
| Reinerio González-Iglesias | |||
| P2860 | cites work | Histidine-proline-rich glycoprotein as a plasma pH sensor. Modulation of its interaction with glycosaminoglycans by ph and metals | Q74263632 |
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| Prions | Q24633319 | ||
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| Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor | Q28363055 | ||
| Eight prion strains have PrP(Sc) molecules with different conformations | Q29617277 | ||
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| Monoclonal antibodies specific for the native, disease-associated isoform of the prion protein | Q30783514 | ||
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| Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation | Q31946943 | ||
| Opposite effects of dextran sulfate 500, the polyene antibiotic MS-8209, and Congo red on accumulation of the protease-resistant isoform of PrP in the spleens of mice inoculated intraperitoneally with the scrapie agent | Q33805383 | ||
| Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody | Q33930771 | ||
| A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseases | Q33952821 | ||
| Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein | Q34294957 | ||
| Suppression of scrapie infection in mice by heteropolyanion 23, dextran sulfate, and some other polyanions | Q35652778 | ||
| Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform | Q36235271 | ||
| Copper binding to octarepeat peptides of the prion protein monitored by mass spectrometry | Q36281890 | ||
| Copper-catalyzed oxidation of the recombinant SHa(29-231) prion protein | Q36297093 | ||
| Location and properties of metal-binding sites on the human prion protein. | Q37104327 | ||
| Sulfated glycans stimulate endocytosis of the cellular isoform of the prion protein, PrPC, in cultured cells. | Q38287981 | ||
| An NMR and molecular modeling study of the site-specific binding of histamine by heparin, chemically modified heparin, and heparin-derived oligosaccharides | Q38313951 | ||
| Heavy metal binding to heparin disaccharides. I. Iduronic acid is the main binding site | Q38328268 | ||
| Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein | Q39673524 | ||
| The molecular theory of polyelectrolyte solutions with applications to the electrostatic properties of polynucleotides | Q39750514 | ||
| Characterization and polyanion-binding properties of purified recombinant prion protein | Q40930836 | ||
| Packaging of proteases and proteoglycans in the granules of mast cells and other hematopoietic cells. A cluster of histidines on mouse mast cell protease 7 regulates its binding to heparin serglycin proteoglycans | Q41310110 | ||
| Cu(2+)-heparin interaction studied by polarimetry | Q41882696 | ||
| Identification of the Cu2+ binding sites in the N-terminal domain of the prion protein by EPR and CD spectroscopy | Q41983149 | ||
| Sulphated glycosaminoglycans prevent the neurotoxicity of a human prion protein fragment | Q41987801 | ||
| Raman spectroscopic study on the copper(II) binding mode of prion octapeptide and its pH dependence | Q43553322 | ||
| Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperone | Q44186617 | ||
| Antibodies inhibit prion propagation and clear cell cultures of prion infectivity | Q46161882 | ||
| Prion protein selectively binds copper(II) ions | Q46492410 | ||
| Folding of prion protein to its native alpha-helical conformation is under kinetic control | Q46690972 | ||
| Oxidative modification of apolipoprotein E in human very-low-density lipoprotein and its inhibition by glycosaminoglycans | Q48182824 | ||
| Reversibility of scrapie inactivation is enhanced by copper | Q48390188 | ||
| Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform | Q48767220 | ||
| Truncated forms of the human prion protein in normal brain and in prion diseases | Q48807964 | ||
| Phosphotungstate shows a heparin-like anticoagulant effect but inhibits heparin. | Q50886592 | ||
| Theory of delocalized ionic binding to polynucleotides: structural and excluded-volume effects | Q52421824 | ||
| Molecular modeling of protein-glycosaminoglycan interactions. | Q52546742 | ||
| Metal-buffered systems. | Q52576438 | ||
| Interaction of the polyelectrolyte heparin with copper(II) and calcium | Q53760474 | ||
| Prolongation of scrapie incubation period by an injection of dextran sulphate 500 within the month before or after infection. | Q54197273 | ||
| Conformational Features and Thermal Stability of Bovine Seminal Plasma Protein PDC-109 Oligomers and Phosphorylcholine-Bound Complexes | Q59287369 | ||
| Refolding and Characterization of Rat Liver Methionine Adenosyltransferase from Escherichia coli Inclusion Bodies | Q59419906 | ||
| Secondary structure and dosage of soluble and membrane proteins by attenuated total reflection Fourier-transform infrared spectroscopy on hydrated films | Q68581487 | ||
| Heparin-like molecules bind differentially to prion-proteins and change their intracellular metabolic fate | Q72656295 | ||
| Dextran Sulphate 500 Delays and Prevents Mouse Scrapie by Impairment of Agent Replication in Spleen | Q72739726 | ||
| Oxidation of heparin-treated low density lipoprotein by peroxidases | Q73110368 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 527-540 | |
| P577 | publication date | 2002-05-01 | |
| P1433 | published in | Journal of Molecular Biology | Q925779 |
| P1476 | title | Prion protein interaction with glycosaminoglycan occurs with the formation of oligomeric complexes stabilized by Cu(II) bridges | |
| P478 | volume | 319 |
| Q38333725 | Biologically Relevant Metal-Cation Binding Induces Conformational Changes in Heparin Oligosaccharides as Measured by Ion Mobility Mass Spectrometry |
| Q46211967 | Biosynthesis of prion protein nucleocytoplasmic isoforms by alternative initiation of translation |
| Q30368863 | Charge neutralization of the central lysine cluster in prion protein (PrP) promotes PrP(Sc)-like folding of recombinant PrP amyloids. |
| Q34185372 | Conformation of prion protein repeat peptides probed by FRET measurements and molecular dynamics simulations |
| Q59419859 | Cu2+ binding triggers αBoPrP assembly into insoluble laminar polymers |
| Q37401407 | Detection of oxidized methionine in selected proteins, cellular extracts and blood serums by novel anti-methionine sulfoxide antibodies |
| Q47223898 | Differential effects of divalent cations on elk prion protein fibril formation and stability |
| Q44320735 | Effect of glycosylphosphatidylinositol anchor-dependent and -independent prion protein association with model raft membranes on conversion to the protease-resistant isoform |
| Q33680310 | Glycosaminoglycan sulphation affects the seeded misfolding of a mutant prion protein |
| Q43101604 | Green fluorescent protein as a reporter of prion protein folding. |
| Q39207578 | Heparan Sulfate and Heparin Promote Faithful Prion Replication in Vitro by Binding to Normal and Abnormal Prion Proteins in Protein Misfolding Cyclic Amplification |
| Q26796383 | Heparan sulfate and heparin interactions with proteins |
| Q33613234 | Heparin binding confers prion stability and impairs its aggregation |
| Q35778031 | Human prion proteins with pathogenic mutations share common conformational changes resulting in enhanced binding to glycosaminoglycans |
| Q44711826 | Inter- and intra-octarepeat Cu(II) site geometries in the prion protein: implications in Cu(II) binding cooperativity and Cu(II)-mediated assemblies |
| Q37110751 | Ligand binding promotes prion protein aggregation--role of the octapeptide repeats |
| Q38347673 | Modulation of prion protein oligomerization, aggregation, and beta-sheet conversion by 4,4'-dianilino-1,1'-binaphthyl-5,5'-sulfonate (bis-ANS). |
| Q51792455 | Molecular interaction between prion protein and GFAP both in native and recombinant forms in vitro. |
| Q33631084 | Oxidation of Helix-3 methionines precedes the formation of PK resistant PrP. |
| Q36012287 | PrP charge structure encodes interdomain interactions |
| Q35009728 | Prion protein misfolding |
| Q24301330 | Prion, amyloid beta-derived Cu(II) ions, or free Zn(II) ions support S-nitroso-dependent autocleavage of glypican-1 heparan sulfate |
| Q36628157 | Prions and their partners in crime |
| Q40677904 | Recombinant prion protein does not possess SOD-1 activity. |
| Q27658157 | Structure of the Flexible Amino-Terminal Domain of Prion Protein Bound to a Sulfated Glycan |
| Q43057853 | Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease |
| Q28506863 | The PrP-like protein Doppel binds copper |
| Q35204580 | The prion protein and neuronal zinc homeostasis |
| Q43068298 | The structural intolerance of the PrP alpha-fold for polar substitution of the helix-3 methionines |
| Q42666355 | Zn2+ mediates high affinity binding of heparin to the αC domain of fibrinogen |
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