Literature DB >> 7756290

Characterization of the internal motions of Escherichia coli ribonuclease HI by a combination of 15N-NMR relaxation analysis and molecular dynamics simulation: examination of dynamic models.

K Yamasaki1, M Saito, M Oobatake, S Kanaya.   

Abstract

The backbone dynamics of Escherichia coli ribonuclease HI (RNase HI) in the picosecond to nanosecond time scale were characterized by a combination of measurements of 15N-NMR relaxation (T1, T2, and NOE), analyzed by a model-free approach, and molecular dynamics (MD) simulation in water. The MD simulations in water were carried out with long-range Coulomb interactions to avoid the artificial fluctuation caused by the cutoff approximation. The model-free analysis of the 15N-NMR relaxation indicated that RNase HI has a rotational correlation time of 10.9 ns at 27 degrees C. The generalized order parameter (S2) for the internal motions varied from 0.15 to 1.0, with an average value of 0.85, which is much larger than that of the RNase H domain of HIV-1 reverse transcriptase (0.78). Large internal motions (small order parameters) were observed in the N-terminal region (Leu2-Lys3), the loop between beta-strands A and B (Cys13-Gly15), the turn between alpha-helix I and beta-strand D (Glu61, His62), the loop between beta-strand D and alpha-helix II (Asp70-Tyr71), the loop between alpha-helices III and IV (Ala93-Lys96), the loop between beta-strand E and alpha-helix V (Gly123-His127), and the C-terminal region (Gln152-Val155). The effective correlation time observed in these regions varied from 0.45 ns (Glu61, Lys96) to 2.2 ns (Leu14). The order parameters calculated from the MD agreed well with those from the NMR experiment, with a few exceptions. The distributions of most of the backbone N-H vectors obtained by MD are approximately consistent with the diffusion-in-a-cone model. These distributions, however, were elliptic, with a long axis perpendicular to the plane defined by the N-H and N-C alpha vectors. Distributions supporting the axial fluctuation model or the jump-between-two-cones model were also observed in the MD simulation.

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Year:  1995        PMID: 7756290     DOI: 10.1021/bi00020a003

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  13 in total

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2.  Key interactions in the immunoglobulin-like structure of apo-neocarzinostatin: evidence from nuclear magnetic resonance relaxation data and molecular dynamics simulations.

Authors:  N Izadi-Pruneyre; Y Blouquit; J Perez; P Minard; M Desmadril; J Mispelter
Journal:  Protein Sci       Date:  2001-11       Impact factor: 6.725

3.  Interpretation of 15N NMR relaxation data of globular proteins using hydrodynamic calculations with HYDRONMR.

Authors:  Pau Bernadó; José García de la Torre; Miquel Pons
Journal:  J Biomol NMR       Date:  2002-06       Impact factor: 2.835

4.  Reorientational contact-weighted elastic network model for the prediction of protein dynamics: comparison with NMR relaxation.

Authors:  Dengming Ming; Rafael Brüschweiler
Journal:  Biophys J       Date:  2006-02-24       Impact factor: 4.033

5.  Protein conformational flexibility prediction using machine learning.

Authors:  Oleg Trott; Keri Siggers; Burkhard Rost; Arthur G Palmer
Journal:  J Magn Reson       Date:  2008-02-01       Impact factor: 2.229

6.  Propagation of experimental uncertainties using the Lipari-Szabo model-free analysis of protein dynamics.

Authors:  D Jin; M Andrec; G T Montelione; R M Levy
Journal:  J Biomol NMR       Date:  1998-11       Impact factor: 2.835

7.  Application of the quasi-spectral density function of (15)N nuclei to the selection of a motional model for model-free analysis.

Authors:  R Ishima; K Yamasaki; K Nagayama
Journal:  J Biomol NMR       Date:  1995-12       Impact factor: 2.835

8.  Spectral densities of nitrogen nuclei in Escherichia coli ribonuclease HI obtained by 15N NMR relaxation and molecular dynamics.

Authors:  R Ishima; K Yamasaki; M Saito; K Nagayama
Journal:  J Biomol NMR       Date:  1995-09       Impact factor: 2.835

9.  Interaction of HIV-1 reverse transcriptase ribonuclease H with an acylhydrazone inhibitor.

Authors:  Qingguo Gong; Lakshmi Menon; Tatiana Ilina; Lena G Miller; Jinwoo Ahn; Michael A Parniak; Rieko Ishima
Journal:  Chem Biol Drug Des       Date:  2010-11-29       Impact factor: 2.817

10.  Comparison of 15N- and 13C-determined parameters of mobility in melittin.

Authors:  L Zhu; F G Prendergast; M D Kemple
Journal:  J Biomol NMR       Date:  1998-07       Impact factor: 2.835

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