471
Views
5
CrossRef citations to date
0
Altmetric
Short Communication

Regional distribution of anchorless prion protein, PrP226*, in the human brain

, , , &
Pages 203-209 | Received 19 Dec 2013, Accepted 27 Feb 2014, Published online: 28 Feb 2014

References

  • Oesch B, Westaway D, Wälchli M, McKinley MP, Kent SB, Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE, et al. A cellular gene encodes scrapie PrP 27-30 protein. Cell 1985; 40:735 - 46; http://dx.doi.org/10.1016/0092-8674(85)90333-2; PMID: 2859120
  • Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, Mehlhorn I, Huang Z, Fletterick RJ, Cohen FE, et al. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. Proc Natl Acad Sci U S A 1993; 90:10962 - 6; http://dx.doi.org/10.1073/pnas.90.23.10962; PMID: 7902575
  • Meyer RK, McKinley MP, Bowman KA, Braunfeld MB, Barry RA, Prusiner SB. Separation and properties of cellular and scrapie prion proteins. Proc Natl Acad Sci U S A 1986; 83:2310 - 4; http://dx.doi.org/10.1073/pnas.83.8.2310; PMID: 3085093
  • Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. Br Med Bull 2003; 66:213 - 39; http://dx.doi.org/10.1093/bmb/66.1.213; PMID: 14522861
  • Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JPM, Zou W-Q, Gambetti P, et al. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. J Biol Chem 2008; 283:30557 - 65; http://dx.doi.org/10.1074/jbc.M801877200; PMID: 18753138
  • Zanusso G, Farinazzo A, Prelli F, Fiorini M, Gelati M, Ferrari S, Righetti PG, Rizzuto N, Frangione B, Monaco S. Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. J Biol Chem 2004; 279:38936 - 42; http://dx.doi.org/10.1074/jbc.M405468200; PMID: 15247220
  • Zou W-Q, Capellari S, Parchi P, Sy M-S, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. J Biol Chem 2003; 278:40429 - 36; http://dx.doi.org/10.1074/jbc.M308550200; PMID: 12917418
  • Curin Serbec V, Bresjanac M, Popovic M, Pretnar Hartman K, Galvani V, Rupreht R, Cernilec M, Vranac T, Hafner I, Jerala R. Monoclonal antibody against a peptide of human prion protein discriminates between Creutzfeldt-Jacob’s disease-affected and normal brain tissue. J Biol Chem 2004; 279:3694 - 8; http://dx.doi.org/10.1074/jbc.M310868200; PMID: 14593100
  • Kosmač M, Koren S, Giachin G, Stoilova T, Gennaro R, Legname G, Serbec VČ. Epitope mapping of a PrP(Sc)-specific monoclonal antibody: identification of a novel C-terminally truncated prion fragment. Mol Immunol 2011; 48:746 - 50; http://dx.doi.org/10.1016/j.molimm.2010.11.012; PMID: 21176851
  • Dvorakova E, Vranac T, Janouskova O, Černilec M, Koren S, Lukan A, Nováková J, Matej R, Holada K, Čurin Šerbec V. Detection of the GPI-anchorless prion protein fragment PrP226* in human brain. BMC Neurol 2013; 13:126; http://dx.doi.org/10.1186/1471-2377-13-126; PMID: 24063733
  • Serban D, Taraboulos A, DeArmond SJ, Prusiner SB. Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins. Neurology 1990; 40:110 - 7; http://dx.doi.org/10.1212/WNL.40.1.110; PMID: 1967489
  • Safar J, Wille H, Itri V, Groth D, Serban H, Torchia M, Cohen FE, Prusiner SB. Eight prion strains have PrP(Sc) molecules with different conformations. Nat Med 1998; 4:1157 - 65; http://dx.doi.org/10.1038/2654; PMID: 9771749
  • Choi YP, Gröner A, Ironside JW, Head MW. Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blot. J Gen Virol 2011; 92:727 - 32; http://dx.doi.org/10.1099/vir.0.026948-0; PMID: 21123539
  • Kuczius T, Koch R, Keyvani K, Karch H, Grassi J, Groschup MH. Regional and phenotype heterogeneity of cellular prion proteins in the human brain. Eur J Neurosci 2007; 25:2649 - 55; http://dx.doi.org/10.1111/j.1460-9568.2007.05518.x; PMID: 17466020
  • Moya KL, Salès N, Hässig R, Créminon C, Grassi J, Di Giamberardino L. Immunolocalization of the cellular prion protein in normal brain. Microsc Res Tech 2000; 50:58 - 65; http://dx.doi.org/10.1002/1097-0029(20000701)50:1<58::AID-JEMT9>3.0.CO;2-5; PMID: 10871549
  • Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996; 39:767 - 78; http://dx.doi.org/10.1002/ana.410390613; PMID: 8651649
  • Schoch G, Seeger H, Bogousslavsky J, Tolnay M, Janzer RC, Aguzzi A, Glatzel M. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease. PLoS Med 2006; 3:e14; http://dx.doi.org/10.1371/journal.pmed.0030014; PMID: 16354106
  • Taraboulos A, Jendroska K, Serban D, Yang SL, DeArmond SJ, Prusiner SB. Regional mapping of prion proteins in brain. Proc Natl Acad Sci U S A 1992; 89:7620 - 4; http://dx.doi.org/10.1073/pnas.89.16.7620; PMID: 1354357
  • Chesebro B, Trifilo M, Race R, Meade-White K, Teng C, LaCasse R, Raymond L, Favara C, Baron G, Priola S, et al. Anchorless prion protein results in infectious amyloid disease without clinical scrapie. Science 2005; 308:1435 - 9; http://dx.doi.org/10.1126/science.1110837; PMID: 15933194
  • Chesebro B, Race B, Meade-White K, Lacasse R, Race R, Klingeborn M, Striebel J, Dorward D, McGovern G, Jeffrey M. Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring. PLoS Pathog 2010; 6:e1000800; http://dx.doi.org/10.1371/journal.ppat.1000800; PMID: 20221436
  • Stöhr J, Watts JC, Legname G, Oehler A, Lemus A, Nguyen H-OB, Sussman J, Wille H, DeArmond SJ, Prusiner SB, et al. Spontaneous generation of anchorless prions in transgenic mice. Proc Natl Acad Sci U S A 2011; 108:21223 - 8; http://dx.doi.org/10.1073/pnas.1117827108; PMID: 22160704
  • Jansen C, Parchi P, Capellari S, Vermeij AJ, Corrado P, Baas F, Strammiello R, van Gool WA, van Swieten JC, Rozemuller AJM. Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. Acta Neuropathol 2010; 119:189 - 97; http://dx.doi.org/10.1007/s00401-009-0609-x; PMID: 19911184
  • Černilec M, Vranac T, Hafner-Bratkovic I, Koren S, Venturini AC, Popović M, Juntes P, Šerbec VČ. Identification of an epitope on the recombinant bovine PrP that is able to elicit a prominent immune response in wild-type mice. Immunol Lett 2007; 113:29 - 39; http://dx.doi.org/10.1016/j.imlet.2007.07.012; PMID: 17884181