Comparisons of NMR spectral quality and success in crystallization demonstrate that NMR and X-ray crystallography are complementary methods for small protein structure determination

David A. Snyder, Yang Chen, Natalia G. Denissova, Thomas Acton, James M. Aramini, Melissa Ciano, Richard Karlin, Jinfeng Liu, Philip Manor, P. A. Rajan, Paolo Rossi, G. V.T. Swapna, Rong Xiao, Burkhard Rost, John Hunt, Gaetano T. Montelione

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Abstract

X-ray crystallography and NMR spectroscopy provide the only sources of experimental data from which protein structures can be analyzed at high or even atomic resolution. The degree to which these methods complement each other as sources of structural knowledge is a matter of debate; it is often proposed that small proteins yielding high quality, readily analyzed NMR spectra are a subset of those that readily yield strongly diffracting crystals. We have examined the correlation between NMR spectral quality and success in structure determination by X-ray crystallography for 159 prokaryotic and eukaryotic proteins, prescreened to avoid proteins providing polydisperse and/or aggregated samples. This study demonstrates that, across this protein sample set, the quality of a protein's [15N-1H]-heteronuclear correlation (HSQC) spectrum recorded under conditions generally suitable for 3D structure determination by NMR, a key predictor of the ability to determine a structure by NMR, is not correlated with successful crystallization and structure determination by X-ray crystallography. These results, together with similar results of an independent study presented in the accompanying paper (Yee, et al., J. Am. Chem. Soc., accompanying paper), demonstrate that X-ray crystallography and NMR often provide complementary sources of structural data and that both methods are required in order to optimize success for as many targets as possible in large-scale structural proteomics efforts.

Original languageEnglish (US)
Pages (from-to)16505-16511
Number of pages7
JournalJournal of the American Chemical Society
Volume127
Issue number47
DOIs
StatePublished - Nov 30 2005

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