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J Biomol NMR. 2011 Jun;50(2):157-65. doi: 10.1007/s10858-011-9508-2. Epub 2011 May 22.

Sequence correction of random coil chemical shifts: correlation between neighbor correction factors and changes in the Ramachandran distribution.

Author information

1
Department of Biology, University of Copenhagen, Ole Maal√łes Vej, Denmark.

Abstract

Random coil chemical shifts are necessary for secondary chemical shift analysis, which is the main NMR method for identification of secondary structure in proteins. One of the largest challenges in the determination of random coil chemical shifts is accounting for the effect of neighboring residues. The contributions from the neighboring residues are typically removed by using neighbor correction factors determined based on each residue's effect on glycine chemical shifts. Due to its unusual conformational freedom, glycine may be particularly unrepresentative for the remaining residue types. In this study, we use random coil peptides containing glutamine instead of glycine to determine the random coil chemical shifts and the neighbor correction factors. The resulting correction factors correlate to changes in the populations of the major wells in the Ramachandran plot, which demonstrates that changes in the conformational ensemble are an important source of neighbor effects in disordered proteins. Glutamine derived random coil chemical shifts and correction factors modestly improve our ability to predict (13)C chemical shifts of intrinsically disordered proteins compared to existing datasets, and may thus improve the identification of small populations of transient structure in disordered proteins.

PMID:
21604143
DOI:
10.1007/s10858-011-9508-2
[Indexed for MEDLINE]

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