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2. Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion. Hafner-Bratkovic I; Bester R; Pristovsek P; Gaedtke L; Veranic P; Gaspersic J; Mancek-Keber M; Avbelj M; Polymenidou M; Julius C; Aguzzi A; Vorberg I; Jerala R J Biol Chem; 2011 Apr; 286(14):12149-56. PubMed ID: 21324909 [TBL] [Abstract][Full Text] [Related]
3. UV-light exposed prion protein fails to form amyloid fibrils. Thakur AK; Rao ChM PLoS One; 2008 Jul; 3(7):e2688. PubMed ID: 18628989 [TBL] [Abstract][Full Text] [Related]
4. Cyclin-dependent kinase 5 phosphorylation of familial prion protein mutants exacerbates conversion into amyloid structure. Rouget R; Sharma G; LeBlanc AC J Biol Chem; 2015 Feb; 290(9):5759-71. PubMed ID: 25572400 [TBL] [Abstract][Full Text] [Related]
5. Copper refolding of prion protein. Wong BS; Vénien-Bryan C; Williamson RA; Burton DR; Gambetti P; Sy MS; Brown DR; Jones IM Biochem Biophys Res Commun; 2000 Oct; 276(3):1217-24. PubMed ID: 11027613 [TBL] [Abstract][Full Text] [Related]
6. Nucleated conformational conversion and the replication of conformational information by a prion determinant. Serio TR; Cashikar AG; Kowal AS; Sawicki GJ; Moslehi JJ; Serpell L; Arnsdorf MF; Lindquist SL Science; 2000 Aug; 289(5483):1317-21. PubMed ID: 10958771 [TBL] [Abstract][Full Text] [Related]
7. Slow spontaneous α-to-β structural conversion in a non-denaturing neutral condition reveals the intrinsically disordered property of the disulfide-reduced recombinant mouse prion protein. Sang JC; Lee CY; Luh FY; Huang YW; Chiang YW; Chen RP Prion; 2012; 6(5):489-97. PubMed ID: 22987112 [TBL] [Abstract][Full Text] [Related]
8. Morphology and secondary structure of stable beta-oligomers formed by amyloid peptide PrP(106-126). Walsh P; Yau J; Simonetti K; Sharpe S Biochemistry; 2009 Jun; 48(25):5779-81. PubMed ID: 19476383 [TBL] [Abstract][Full Text] [Related]
9. Tetracysteine-tagged prion protein allows discrimination between the native and converted forms. Gaspersic J; Hafner-Bratkovic I; Stephan M; Veranic P; Bencina M; Vorberg I; Jerala R FEBS J; 2010 May; 277(9):2038-50. PubMed ID: 20345906 [TBL] [Abstract][Full Text] [Related]
11. A 3-disulfide mutant of mouse prion protein expression, oxidative folding, reductive unfolding, conformational stability, aggregation and isomerization. Lu BY; Chang JY Arch Biochem Biophys; 2007 Apr; 460(1):75-84. PubMed ID: 17320038 [TBL] [Abstract][Full Text] [Related]
12. Autocatalytic conversion of recombinant prion proteins displays a species barrier. Baskakov IV J Biol Chem; 2004 Feb; 279(9):7671-7. PubMed ID: 14668351 [TBL] [Abstract][Full Text] [Related]
13. Biochemical and structural studies of the prion protein polymorphism. Petchanikow C; Saborio GP; Anderes L; Frossard MJ; Olmedo MI; Soto C FEBS Lett; 2001 Dec; 509(3):451-6. PubMed ID: 11749972 [TBL] [Abstract][Full Text] [Related]
14. Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation. Kundu B; Maiti NR; Jones EM; Surewicz KA; Vanik DL; Surewicz WK Proc Natl Acad Sci U S A; 2003 Oct; 100(21):12069-74. PubMed ID: 14519851 [TBL] [Abstract][Full Text] [Related]
15. Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form. Vanik DL; Surewicz WK J Biol Chem; 2002 Dec; 277(50):49065-70. PubMed ID: 12372829 [TBL] [Abstract][Full Text] [Related]
16. Fibril conformation as the basis of species- and strain-dependent seeding specificity of mammalian prion amyloids. Jones EM; Surewicz WK Cell; 2005 Apr; 121(1):63-72. PubMed ID: 15820679 [TBL] [Abstract][Full Text] [Related]
17. Effect of hydrophobic mutations in the H2-H3 subdomain of prion protein on stability and conversion in vitro and in vivo. Hafner-Bratkovič I; Gaedtke L; Ondracka A; Veranič P; Vorberg I; Jerala R PLoS One; 2011; 6(9):e24238. PubMed ID: 21909425 [TBL] [Abstract][Full Text] [Related]
18. Disulfide mapping reveals the domain swapping as the crucial process of the structural conversion of prion protein. Hafner-Bratkovič I; Jerala R Prion; 2011; 5(2):56-9. PubMed ID: 21555920 [TBL] [Abstract][Full Text] [Related]
19. Inter-oligomer interactions of the human prion protein are modulated by the polymorphism at codon 129. Gerber R; Voitchovsky K; Mitchel C; Tahiri-Alaoui A; Ryan JF; Hore PJ; James W J Mol Biol; 2008 Aug; 381(1):212-20. PubMed ID: 18597782 [TBL] [Abstract][Full Text] [Related]
20. Structural determinants in prion protein folding and stability. Benetti F; Biarnés X; Attanasio F; Giachin G; Rizzarelli E; Legname G J Mol Biol; 2014 Nov; 426(22):3796-3810. PubMed ID: 25280897 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]