Iron responsive element RNA flexibility described by NMR and isotropic reorientational eigenmode dynamics
被引:27
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作者:
Showalter, SA
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机构:Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Showalter, SA
Baker, NA
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机构:Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Baker, NA
Tang, CG
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机构:Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Tang, CG
Hall, K
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机构:
Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
Hall, K
[1
]
机构:
[1] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Ctr Computat Biol, St Louis, MO 63110 USA
IRE RNA;
molecular dynamics;
NMR structure and dynamics;
RED analysis;
D O I:
10.1007/s10858-005-7948-2
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The first example of the application of reorientational eigenmode dynamics (RED) to RNA is shown here for the small and floppy Iron Responsive Element (IRE) RNA hairpin. Order parameters calculated for bases and riboses from a 12 ns molecular dynamics trajectory are compared to experimentally determined order parameters from C-13-H-1 NMR relaxation experiments, and shown to be in qualitative agreement. Given the small size of the IRE hairpin and its very flexible loop, isotropic RED (iRED) was also used to analyze the trajectory in order to describe its dynamic motions. iRED analysis shows that the global and internal dynamics of the IRE are not rigorously separable, which will result in inaccurate experimental order parameters. In addition, the iRED analysis described the many correlated motions that comprise the dynamics of the IRE RNA. The combined use of NMR relaxation, RED, and iRED provide a uniquely detailed description of IRE RNA dynamics.