Triple-resonance experiments facilitate the determination of sequence-specific resonance assignments of medium-sized ~3C]SN-enriched proteins. Some triple-resonance experiments can also be used to obtain information about amino acid spin-system topologies by proper delay tuning. The constant-time PF
Phase labeling of C−H and C−C spin-system topologies: Application in PFG-HACANH and PFG-HACA(CO)NH triple-resonance experiments for determining backbone resonance assignments in proteins
✍ Scribed by Wenqing Feng; Carlos B. Rios; Gaetano T. Montelione
- Publisher
- Springer Netherlands
- Year
- 1996
- Tongue
- English
- Weight
- 603 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0925-2738
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✦ Synopsis
Triple-resonance experiments can be designed to provide useful information on spin-system topologies. In this paper we demonstrate optimized proton and carbon versions of PFG-CT-HACANH and PFG-CT-HACA(CO)NH 'straight-through' triple-resonance experiments that allow rapid and almost complete assignments of backbone H a, 13C~, ~SN and H N resonances in small proteins. This work provides a practical guide to using these experiments for determining resonance assignments in proteins, and for identifying both intraresidue and sequential connections involving glycine residues. Two types of delay tunings within these pulse sequences provide phase discrimination of backbone Gly C a and H a resonances: (i) C-H phase discrimination by tuning of the refocusing period Xaf; (ii) C-C phase discrimination by tuning of the ~3C constant-time evolution period 2T~. For small proteins, C-C phase tuning provides better S/N ratios in PFG-CT-HACANH experiments while C-H phase tuning provides better S/N ratios in PFG-CT-HACA(CO)NH. These same principles can also be applied to triple-resonance experiments utilizing 13C-13C COSY and TOCSY transfer from peripheral side-chain atoms with detection of backbone amide protons for classification of side-chain spin-system topologies. Such data are valuable in algorithms for automated analysis of resonance assignments in proteins.
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