Literature DB >> 24549096

Heterogeneous seeding of HET-s(218-289) and the mutability of prion structures.

William Wan1, Gerald Stubbs1.   

Abstract

One fundamental property of prions is the formation of strains-prions that have distinct biological effects, despite a common amino acid sequence. The strain phenomenon is thought to be caused by the formation of different molecular structures, each encoding for a particular biological activity. While the precise mechanism of the formation of strains is unknown, they tend to arise following environmental changes, such as passage between different species. One possible mechanism discussed here is heterogeneous seeding; the formation of a prion nucleated by a different molecular structure. While heterogeneous seeding is not the only mechanism of prion mutation, it is consistent with some observations on species adaptation and drug resistance. Heterogeneous seeding provides a useful framework to understand how prions can adapt to new environmental conditions and change biological phenotypes.

Entities:  

Keywords:  amyloid; fiber diffraction; prion structure; protein aggregation; self-propagation

Mesh:

Substances:

Year:  2014        PMID: 24549096      PMCID: PMC4189887          DOI: 10.4161/pri.28126

Source DB:  PubMed          Journal:  Prion        ISSN: 1933-6896            Impact factor:   3.931


  32 in total

1.  Structural studies of the scrapie prion protein by electron crystallography.

Authors:  Holger Wille; Melissa D Michelitsch; Vincent Guenebaut; Surachai Supattapone; Ana Serban; Fred E Cohen; David A Agard; Stanley B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

2.  Amyloid aggregates of the HET-s prion protein are infectious.

Authors:  Marie-Lise Maddelein; Suzana Dos Reis; Stéphane Duvezin-Caubet; Bénédicte Coulary-Salin; Sven J Saupe
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

3.  Domain organization and structure-function relationship of the HET-s prion protein of Podospora anserina.

Authors:  Axelle Balguerie; Suzana Dos Reis; Christiane Ritter; Stéphane Chaignepain; Bénédicte Coulary-Salin; Vincent Forge; Katell Bathany; Ioan Lascu; Jean-Marie Schmitter; Roland Riek; Sven J Saupe
Journal:  EMBO J       Date:  2003-05-01       Impact factor: 11.598

4.  Atomic-resolution three-dimensional structure of HET-s(218-289) amyloid fibrils by solid-state NMR spectroscopy.

Authors:  Hélène Van Melckebeke; Christian Wasmer; Adam Lange; Eiso Ab; Antoine Loquet; Anja Böckmann; Beat H Meier
Journal:  J Am Chem Soc       Date:  2010-10-06       Impact factor: 15.419

Review 5.  Molecular biology of prion diseases.

Authors:  S B Prusiner
Journal:  Science       Date:  1991-06-14       Impact factor: 47.728

6.  Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+].

Authors:  Y O Chernoff; S L Lindquist; B Ono; S G Inge-Vechtomov; S W Liebman
Journal:  Science       Date:  1995-05-12       Impact factor: 47.728

7.  Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters.

Authors:  R A Bessen; R F Marsh
Journal:  J Gen Virol       Date:  1992-02       Impact factor: 3.891

8.  Synthetic mammalian prions.

Authors:  Giuseppe Legname; Ilia V Baskakov; Hoang-Oanh B Nguyen; Detlev Riesner; Fred E Cohen; Stephen J DeArmond; Stanley B Prusiner
Journal:  Science       Date:  2004-07-30       Impact factor: 47.728

9.  Prion and non-prion amyloids of the HET-s prion forming domain.

Authors:  Raimon Sabaté; Ulrich Baxa; Laura Benkemoun; Natalia Sánchez de Groot; Bénédicte Coulary-Salin; Marie-Lise Maddelein; Laurent Malato; Salvador Ventura; Alasdair C Steven; Sven J Saupe
Journal:  J Mol Biol       Date:  2007-05-22       Impact factor: 5.469

10.  [URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae.

Authors:  R B Wickner
Journal:  Science       Date:  1994-04-22       Impact factor: 47.728

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  2 in total

1.  Structural studies of truncated forms of the prion protein PrP.

Authors:  William Wan; Holger Wille; Jan Stöhr; Amy Kendall; Wen Bian; Michele McDonald; Sarah Tiggelaar; Joel C Watts; Stanley B Prusiner; Gerald Stubbs
Journal:  Biophys J       Date:  2015-03-24       Impact factor: 4.033

2.  Truncated forms of the prion protein PrP demonstrate the need for complexity in prion structure.

Authors:  William Wan; Jan Stöhr; Amy Kendall; Gerald Stubbs
Journal:  Prion       Date:  2015-09-01       Impact factor: 3.931

  2 in total

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