Abstract
A new method to selectively detect the ring resonances of the aromatic residues in 15N-labelled proteins is presented. The experiment consists of a 2D 1H TOCSY sequence withremoval of the amide signals via 15N-filtering. Experiments are acquired in the absence andpresence of water inversion; combining the two spectra allows selective observation of thetyrosine ring resonances and enables the identification of their delta andepsilon ring protons. The experiment is demonstrated on a 15N-labelled sample of Photoactive Yellow Protein and isshown to give good selectivity for tyrosine ring resonances under a wide range oftemperatures and pH values.
| Original language | English |
|---|---|
| Pages (from-to) | 313-6 |
| Number of pages | 4 |
| Journal | Journal of Biomolecular NMR |
| Volume | 9 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Apr 1997 |