MEASUREMENT OF N-15-H-1 COUPLING-CONSTANTS IN UNIFORMLY N-15-LABELED PROTEINS - APPLICATION TO THE PHOTOACTIVE YELLOW PROTEIN

Citation
P. Dux et al., MEASUREMENT OF N-15-H-1 COUPLING-CONSTANTS IN UNIFORMLY N-15-LABELED PROTEINS - APPLICATION TO THE PHOTOACTIVE YELLOW PROTEIN, Journal of biomolecular NMR, 10(3), 1997, pp. 301-306
Citations number
27
Categorie Soggetti
Biology,Spectroscopy
Journal title
ISSN journal
09252738
Volume
10
Issue
3
Year of publication
1997
Pages
301 - 306
Database
ISI
SICI code
0925-2738(1997)10:3<301:MONCIU>2.0.ZU;2-W
Abstract
A modified HNHB experiment is presented that allows the determination of J(NH) coupling constants directly from the ratio of cross-peak to d iagonal-peak intensities. The experiment was applied to the photoactiv e yellow protein (PYP) and yielded the magnitude of 117 (3)J(NHbeta) c oupling constants. In addition, 29 (3)J(NHalpha(i-1)) coupling constan ts could be measured, providing information about the backbone angle p si. These data, in conjunction with the magnitudes of the (3)J((HHalph a)-H-N) coupling constants obtained from the HNHA spectrum, effectivel y discriminate the two possibilities for the stereospecific assignment of the H-alpha resonances in glycine residues. For all eight glycine residues in PYP that were not subject to conformational averaging and had non-degenerate H-alpha resonance frequencies, the J-coupling data, together with limited NOE data, yielded the stereospecific assignment of the H-alpha resonances for these residues. In addition, reliable a nd precise phi,psi dihedral constraints were also derived for these re sidues from the J-coupling data.