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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of biomolecular NMR 3 (1993), S. 627-638 
    ISSN: 1573-5001
    Keywords: Hydrogen exchange ; NOESY ; ROESY ; Water ; Protein ; 2D NMR ; Calcineurin B
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary A rapid and sensitive 2D approach is presented for measuring amide proton exchange rates and the NOE interaction between amide protons and water. The approach is applicable to uniformly 13C/15N-enriched proteins and can measure magnetization exchange rates in the 0.02 to 〉20s−1 range. The experiments rely on selective excitation of the water resonance, coupled with purging of underlying Hα resonances, followed by NOESY-or ROESY-type transfer to amide protons, which are dispersed by the amide 15N frequencies in an HSQC-type experiment. Two separate but interleaved experiments, with and without selective inversion of the H2O resonance, yield quantitative results. The method is demonstrated for a sample of the calcium-binding protein calcineurin B. Results indicate rapid amide exchange for the five calcineurin B residues that are analogous to the five rapidly exchanging residues in the ‘central helix’ of the homologous protein calmodulin.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of biomolecular NMR 1 (1991), S. 439-446 
    ISSN: 1573-5001
    Keywords: 2D NMR ; J couplings ; Protein structure ; Isotopic labeling ; Triple resonance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary 15N-Cα and15N-C′ J couplings were measured for the backbone of staphylococcal nuclease, uniformly enriched with15N and13C. It is found that theIJC'N coupling is similar for β-sheet, J=14.8 ± 0.5 and for α-helix, J = 14.8 ± 0.4 but tends to be larger for the unstructured N- and C-terminal ends of the protein (J=15.6 ± 0.5). On average,1JNCα are smaller for α-helical residues (J=9.6 ± 0.3 Hz) compared to β-sheet (J=10.9 ± 0.8 Hz) and a substantial difference is observed for2JNCα in α-helices (J=6.4 ± 0.4 Hz) and β-sheets (J=8.3 ± 0.8 Hz).
    Type of Medium: Electronic Resource
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