Backbone dynamics of calcium-loaded calbindin D9k studied by two-dimensional proton-detected nitrogen-15 NMR spectroscopy
- 1 May 1992
- journal article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 31 (20) , 4856-4866
- https://doi.org/10.1021/bi00135a017
Abstract
Backbone dynamics of calcium-loaded calbindin D9k have been investigated by two-dimensional proton-detected heteronuclear nuclear magnetic resonance spectroscopy, using a uniformly 15N enriched protein sample. Spin-lattice relaxation rate constants, spin-spin relaxation rate constants, and steady-state [1H]-15N nuclear Overhauser effects were determined for 71 of the 72 backbone amide 15N nuclei. The relaxation parameters were analyzed using a model-free formalism that incorporates the overall rotational correlation time of the molecule, and a generalized order parameter (S2) and an effective internal correlation time for each amide group. Calbindin D9k contains two helix-loop-helix motifs joined by a linker loop at one end of the protein and a beta-type interaction between the two calcium-binding loops at the other end. The amplitude of motions for the calcium-binding loops and the helices are similar, as judged from the average S2 values of 0.83 +/- 0.05 and 0.85 +/- 0.04, respectively. The linker region joining the two calcium-binding subdomains of the molecule has a significantly higher flexibility, as indicated by a substantially lower average S2 value of 0.59 +/- 0.23. For residues in the linker loop and at the C-terminus, the order parameter is further decomposed into separate order parameters for motional processes on two distinct time scales. The effective correlation times are significantly longer for helices I and IV than for helices II and III or for the calcium-binding loops. Residue by residue comparisons reveal correlations of the order parameters with both the crystallographic B-factors and amide proton exchange rates, despite vast differences in the time scales to which these properties are sensitive. The order parameters are also utilized to distinguish regions of the NMR-derived three-dimensional structure of calbindin D9k that are poorly defined due to inherently high flexibility, from poorly defined regions with average flexibility but a low density of structural constraints.Keywords
This publication has 40 references indexed in Scilit:
- Three-dimensional solution structure of calcium-loaded porcine calbindin D9k determined by nuclear magnetic resonance spectroscopyBiochemistry, 1992
- Molecular basis for co-operativity in Ca2+ binding to calbindin D9k: 1H nuclear magnetic resonance studies of (Cd2+)1-bovine calbindin D9kJournal of Molecular Biology, 1991
- Influence of cross-correlation between dipolar and anisotropic chemical shift relaxation mechanisms upon longitudinal relaxation rates of 15N in macromoleculesChemical Physics Letters, 1990
- Analysis of the backbone dynamics of interleukin-1.beta. using two-dimensional inverse detected heteronuclear nitrogen-15-proton NMR spectroscopyBiochemistry, 1990
- Deviations from the simple two-parameter model-free approach to the interpretation of nitrogen-15 nuclear magnetic relaxation of proteinsJournal of the American Chemical Society, 1990
- Identification of an isoaspartyl linkage formed upon deamidation of bovine calbindin D9k and structural characterization by 2D proton NMRBiochemistry, 1989
- Proline isomerism leads to multiple folded conformations of calbindin D9k: direct evidence from two-dimensional 1H NMR spectroscopy.Proceedings of the National Academy of Sciences, 1989
- [7] Detection of insensitive nucleiPublished by Elsevier ,1989
- Advances in Chemical PhysicsAdvances in Chemical Physics, 1988
- Effects of Diffusion on Free Precession in Nuclear Magnetic Resonance ExperimentsPhysical Review B, 1954