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Structures of Larger Proteins in Solution: Three- and Four-Dimensional Heteronuclear NMR Spectroscopy
Author(s) -
G. Marius Clore,
Angela M. Gronenborn
Publication year - 1991
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.2047852
Subject(s) - heteronuclear molecule , nuclear magnetic resonance spectroscopy , chemistry , heteronuclear single quantum coherence spectroscopy , transverse relaxation optimized spectroscopy , two dimensional nuclear magnetic resonance spectroscopy , nuclear magnetic resonance , spectroscopy , pulse sequence , molecule , fluorine 19 nmr , analytical chemistry (journal) , crystallography , physics , stereochemistry , organic chemistry , quantum mechanics
Three- and four-dimensional heteronuclear nuclear magnetic resonance (NMR) spectroscopy offers dramatic improvements in spectral resolution by spreading through-bond and through-space correlations in three and four orthogonal frequency axes. Simultaneously, large heteronuclear couplings are exploited to circumvent problems due to the larger linewidths that are associated with increasing molecular weight. These novel experiments have been designed to extend the application of NMR as a method for determining three-dimensional structures of proteins in solution beyond the limits of conventional two-dimensional NMR (approximately 100 residues) to molecules in the 150- to 300-residue range. This potential has recently been confirmed with the determination of the high-resolution NMR structure of a protein greater than 150 residues, namely, interleukin-1 beta.

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