Published June 2001
| Version v1
Journal article
A new approach for obtaining sequential assignment of large proteins
Creators
- 1. University of Helsinki, Institute of Biotechnology, NMR Laboratory (Finland)
- 2. VTT Biotechnology (Finland)
Description
A novel NMR experiment for obtaining sequential assignment of large proteins and protein complexes is described. The proposed method takes full advantage of transverse relaxation optimized spectroscopy (TROSY) and utilizes spin-state-selection to distinguish between intraresidual and sequential connectivities in the HNCA-TROSY-type correlation experiment. Thus, the intra- and interresidual cross peaks can be identified without relaying magnetization via carbonyl carbon, which relaxes very rapidly at the high magnetic fields where TROSY is most efficient. In addition, the presented method enables measurement of several scalar and residual dipolar couplings, which can potentially be used for structure determination of large proteins
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Biomolecular NMR
- Journal Volume
- 20
- Journal Issue
- 2
- Journal Page Range
- p. 127-133
- ISSN
- 0925-2738
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 39109716
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CARBON; CARBONYLS; COUPLINGS; MAGNETIC FIELDS; MAGNETIZATION; PROTEIN STRUCTURE; PROTEINS; RELAXATION; SCALARS; SPECTROSCOPY; SPIN
- Descriptors DEC
- ANGULAR MOMENTUM; ELEMENTS; NONMETALS; ORGANIC COMPOUNDS; PARTICLE PROPERTIES
Optional Information
- Copyright
- Copyright (c) 2001 Kluwer Academic Publishers