Backbone dynamics measurements on leukemia inhibitory factor, a rigid four-helical bundle cytokine
Details
Publication Year 2000-04,Volume 9,Issue #4,Page 671-682
Journal Title
PROTEIN SCIENCE
Publication Type
Journal Article
Abstract
The backbone dynamics of the four-helical bundle cytokine leukemia inhibitory factor (LIF) have been investigated using N-15 NMR relaxation and amide proton exchange measurements on a murine-human chimera, MH35-LIF For rapid backbone motions (on a time scale of 10 ps to 100 ns), as probed by N-15 relaxation measurements, the dynamics parameters were calculated using the model-free formalism incorporating the model selection approach. The principal components of the inertia tensor of MH35-LIF as calculated from its NMR structure, were 1:0.98:0.38. The global rotational motion of the molecule was, therefore, assumed to be axially symmetric in the analysis of its relaxation data. This yielded a diffusion anisotropy D-\\/D-perpendicular to of 1.31 and an effective correlation time (4D(perpendicular to) + 2D(\\))(-1) of 8.9 ns. The average values of the order parameters (S-2) for the four helices, the long interhelical loops, and the N-terminus were 0.91, 0.84, and 0.65, respectively, indicating that LIF is fairly rigid in solution, except at the N-terminus. The S2 values for the long interhelical loops of MH35-LIF were higher than those of their counterparts in short-chain members of the four-helical bundle cytokine family. Residues involved in LIF receptor binding showed no consistent pattern of backbone mobilities, with SZ values ranging from 0.71 to 0.95, but residues contributing to receptor binding site III had relatively lower S2 values, implying higher amplitude motions than for the backbone of sites I and Il. In the relatively slow motion regime, backbone amide exchange measurements showed that a number of amides from the helical bundle exchanged extremely slowly, persisting for several months in (H2O)-H-2 at 37 degrees C. Evidence for local unfolding was considered, and correlations among various structure-related parameters and the backbone amide exchange rates were examined. Both sets of data concur in showing that LIF is one of the most rigid four-helical bundle cytokines.
Publisher
CAMBRIDGE UNIV PRESS
Keywords
N-15 NMR RELAXATION; COLONY-STIMULATING FACTOR; MODEL-FREE APPROACH; ANISOTROPIC ROTATIONAL DIFFUSION; MAGNETIC-RESONANCE RELAXATION; EGG-WHITE LYSOZYME; HYDROGEN-EXCHANGE; SECONDARY STRUCTURE; RECEPTOR-BINDING; STAPHYLOCOCCAL NUCLEASE
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Creation Date: 2000-04-01 12:00:00
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