Consistent blind protein structure generation from NMR chemical shift data

TitleConsistent blind protein structure generation from NMR chemical shift data
Publication TypeJournal Article
Year of Publication2008
AuthorsShen, Y., Lange O., Delaglio F., Rossi P., Aramini J. M., Liu G., Eletsky A., Wu Y., Singarapu K. K., Lemak A., Ignatchenko A., Arrowsmith C. H., Szyperski T., Montelione G. T., Baker D., & Bax A.
JournalProceedings of the National Academy of Sciences of the United States of America
Volume105
Issue12
Pagination4685-90
Date Published2008 Mar 25
ISSN1091-6490
KeywordsCollaborative Publication, Genomics, Magnetic Resonance Spectroscopy, Models, Molecular, Protein Structure, Secondary, Proteins, Software, Thermodynamics, Ubiquitin
Abstract

Protein NMR chemical shifts are highly sensitive to local structure. A robust protocol is described that exploits this relation for de novo protein structure generation, using as input experimental parameters the (13)C(alpha), (13)C(beta), (13)C', (15)N, (1)H(alpha) and (1)H(N) NMR chemical shifts. These shifts are generally available at the early stage of the traditional NMR structure determination process, before the collection and analysis of structural restraints. The chemical shift based structure determination protocol uses an empirically optimized procedure to select protein fragments from the Protein Data Bank, in conjunction with the standard ROSETTA Monte Carlo assembly and relaxation methods. Evaluation of 16 proteins, varying in size from 56 to 129 residues, yielded full-atom models that have 0.7-1.8 A root mean square deviations for the backbone atoms relative to the experimentally determined x-ray or NMR structures. The strategy also has been successfully applied in a blind manner to nine protein targets with molecular masses up to 15.4 kDa, whose conventional NMR structure determination was conducted in parallel by the Northeast Structural Genomics Consortium. This protocol potentially provides a new direction for high-throughput NMR structure determination.

Alternate JournalProc. Natl. Acad. Sci. U.S.A.
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