Literature DB >> 24771297

Protocol for aerosol-free recombinant production and NMR analysis of prion proteins.

Peter Rehbein1, Krishna Saxena, Kai Schlepckow, Harald Schwalbe.   

Abstract

The central hallmark of prion diseases is the misfolding of cellular prion protein (PrP(C)) into a disease-associated aggregated isoform known as scrapie prion protein (PrP(Sc)). NMR spectroscopy has made many essential contributions to the characterization of recombinant PrP in its folded, unfolded and aggregated states. Recent studies reporting on de novo generation of prions from recombinant PrP and infection of animals using prion aerosols suggest that adjustment of current biosafety measures may be necessary, particularly given the relatively high protein concentrations required for NMR applications that favor aggregation. We here present a protocol for the production of recombinant PrP under biosafety level 2 conditions that avoids entirely exposure of the experimenter to aerosols that might contain harmful PrP aggregates. In addition, we introduce an NMR sample tube setup that allows for safe handling of PrP samples at the spectrometer that usually is not part of a dedicated biosafety level 2 laboratory.

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Year:  2014        PMID: 24771297     DOI: 10.1007/s10858-014-9831-5

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  33 in total

1.  The α-helical C-terminal domain of full-length recombinant PrP converts to an in-register parallel β-sheet structure in PrP fibrils: evidence from solid state nuclear magnetic resonance.

Authors:  Robert Tycko; Regina Savtchenko; Valeriy G Ostapchenko; Natallia Makarava; Ilia V Baskakov
Journal:  Biochemistry       Date:  2010-11-09       Impact factor: 3.162

2.  Expression and purification of full-length recombinant PrP of high purity.

Authors:  Natallia Makarava; Ilia V Baskakov
Journal:  Methods Mol Biol       Date:  2008

3.  Aerosol transmission of chronic wasting disease in white-tailed deer.

Authors:  Nathaniel D Denkers; Jeanette Hayes-Klug; Kelly R Anderson; Davis M Seelig; Nicholas J Haley; Sallie J Dahmes; David A Osborn; Karl V Miller; Robert J Warren; Candace K Mathiason; Edward A Hoover
Journal:  J Virol       Date:  2012-11-21       Impact factor: 5.103

4.  Generating a prion with bacterially expressed recombinant prion protein.

Authors:  Fei Wang; Xinhe Wang; Chong-Gang Yuan; Jiyan Ma
Journal:  Science       Date:  2010-01-28       Impact factor: 47.728

5.  Prion protein NMR structures of cats, dogs, pigs, and sheep.

Authors:  Dominikus A Lysek; Christian Schorn; Lucas G Nivon; Vicent Esteve-Moya; Barbara Christen; Luigi Calzolai; Christine von Schroetter; Francesco Fiorito; Torsten Herrmann; Peter Güntert; Kurt Wüthrich
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-12       Impact factor: 11.205

6.  Core structure of amyloid fibrils formed by residues 106-126 of the human prion protein.

Authors:  Patrick Walsh; Karen Simonetti; Simon Sharpe
Journal:  Structure       Date:  2009-03-11       Impact factor: 5.006

7.  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

8.  A novel expression system for production of soluble prion proteins in E. coli.

Authors:  Romany N N Abskharon; Stephanie Ramboarina; Hassan El Hassan; Wael Gad; Marcin I Apostol; Gabriele Giachin; Giuseppe Legname; Jan Steyaert; Joris Messens; Sameh H Soror; Alexandre Wohlkonig
Journal:  Microb Cell Fact       Date:  2012-01-10       Impact factor: 5.328

9.  Aerosol and nasal transmission of chronic wasting disease in cervidized mice.

Authors:  Nathaniel D Denkers; Davis M Seelig; Glenn C Telling; Edward A Hoover
Journal:  J Gen Virol       Date:  2010-02-17       Impact factor: 3.891

10.  Recombinant prion protein induces a new transmissible prion disease in wild-type animals.

Authors:  Natallia Makarava; Gabor G Kovacs; Olga Bocharova; Regina Savtchenko; Irina Alexeeva; Herbert Budka; Robert G Rohwer; Ilia V Baskakov
Journal:  Acta Neuropathol       Date:  2010-01-06       Impact factor: 17.088

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