Published June 2001 | Version v1
Journal article

A new approach for obtaining sequential assignment of large proteins

  • 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