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
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.