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Abstrakty
Dicer is an enzyme responsible for processing double-stranded RNAs and plays a key role in an RNAi mechanism. Structural insight into the Dicer is provided by the crystal structure of eukaryotic Dicer from Giardia intestinalis. It has been proposed that the structure has three structurally rigid regions that are connected by the flexible hinges. Flexibility of the Dicer is believed to be a critical feature for its function. Spatial arrangement of the RNA-recognition and the catalytic regions is crucial for producing small RNAs of defined length. It has been suggested that in the Giardia Dicer a Platform domain may help in specific arrangement of these regions. To learn more about the role of the Platform domain in Giardia Dicer, we have performed molecular dynamics (MD) simulations of the whole Dicer (WT Dicer) and the Dicer with a deleted platform domain (delta Plf Dicer). The MD simulations were carried out in an implicit solvent model with two implementations of analytic Generalized Born (GB) solvation model in CHARMM: GBMV (Generalized Born using Molecular Volume) and GBSW (Generalized Born with simple Switching). To detect the key global motions of the Dicer, a principal component analysis (PCA) of the obtained MD trajectories has been used. To further explore the motion of the Dicer, we performed a domain motion analysis with the DYNDOM program. The simulations show that both WT Dicer and delta Plf Dicer display flexibility which can be described as a movement of two or three domains. The removal of the Platform substantially changed the flexibility and arrangement of these domains. During the MD simulations of delta Plf Dicer an large movement of the RNA-recognition domain was observed.
Rocznik
Tom
Strony
97--104
Opis fizyczny
Bibliogr. 24 poz., rys.
Twórcy
autor
autor
autor
autor
autor
autor
autor
- Institute of Bioorganic Chemistry, Polish Academy of Sciences ul. Noskowskiego 12/14, 61-704 Poznań, Poland, joanna.sarzynska@ibch.poznan.pl
Bibliografia
- [1] I.J. MacRae, K. Zhou, F. Li, A. Repic, A.N. Brooks, W.Z. Cande, P.D. Adams, J.A. Doudna, Structural Basis for Double-Stranded RNA Processing by Dicer, Science 311,195-198 (2006).
- [2] I.J. MacRae, K. Zhou, J.A. Doudna, Structural Determinants of RNA Recognition and Cleavage by Dicer. Nat. Struct. Mol. Biol. 14, 934-940 (2007).
- [3] I.J. MacRae, F. Li, K. Zhou, W.Z. Cande, J.A. Doudna, Structure of Dicer and Mechanistic Implications for RNAi. Cold Spring Harb. Symp. Quant. Biol. 71, 73-80 (2006).
- [4] M. Dlakic, DUF283 Domain of Dicer Proteins Has a Double-Stranded RNA-Binding Fold. Bioinformatics 22, 2711-2714 (2006).
- [5] H.T. Allawi, M.W. Kaiser, A.V. Onufriev, W.P. Ma, A.E. Brogaard, D.A. Case, B.P. Neri, V.I. Lyamichev, Modeling of Flap Endonuclease Interactions With DNA Substrate. Journal of Molecular Biology 328, 537-554 (2003).
- [6] J. Chocholousova, M. Feig, Implicit Solvent Simulations of DNA and DNA-Protein Complexes: Agreement with Explicit Solvent Vs Experiment, Journal of Physical Chemistry B 110, 17240-17251 (2006).
- [7] V. Hornak, A. Okur, R.C. Rizzo, C. Simmerling, HIV-1Protease Flaps Spontaneously Open and Reclose in Molecular Dynamics Simulations. Proceedings of the National Academy of Sciences of the United States of America 103, 915-920 (2006).
- [8] M.S. Lee, F.R. Salsbury, C.L. Brooks, Novel Generalized Born Methods. Journal of Chemical Physics 116, 10606-10614 (2002).
- [9] M.S. Lee, M. Feig, F.R. Salsbury, Jr., C.L. Brooks, III, New Analytic Approximation to the Standard Molecular Volume Definition and Its Application to Generalized Born Calculations. J. Comput. Chem. 24, 1348-1356 (2003).
- [10] W. Im, M.S. Lee, C.L. Brooks, III, Generalized Born Model With a Simple Smoothing Function. J. Comput. Chem. 24, 1691-1702 (2003).
- [11] J. Chen, W. Im, C. L. Brooks, III, Balancing Solvation and Intramolecular Interactions: Toward a Consistent Generalized Born Force Field. J. Am. Chem. Soc. 128, 3728-3736 (2006).
- [12] A. Sali, T.L. Blundell, Comparative Protein Modelling by Satisfaction of Spatial Restraints, J. Mol. Biol. 234, 779-815 (1993).
- [13] B.R. Brooks, R.E. Bruccoleri, B.D. Olafson, D.J. States, S. Swaminathan, M. Karplus, CHARMM: A Program for Macromolecular Energy, Minimization, and Dynamics Calculations. J. Comp. Chem. 4, 187-217 (1983).
- [14] B.R. Brooks, C. L. Brooks, A. D. Mackerell, L. Nilsson, R. J. Petrella, B. Roux, Y. Won, G. Archontis, C. Bartels, S. Boresch, A. Caflisch, L. Caves, Q. Cui, A.R. Dinner, M. Feig, S. Fischer, J. Gao, M. Hodoscek, W. Im, K. Kuczera, T. Lazaridis, J. Ma, V. Ovchinnikov, E. Paci, R.W. Pastor, C.B. Post, J.Z. Pu, M. Schaefer, B. Tidor, R. M. Venable, H. L. Woodcock, X. Wu, W. Yang, D.M. York, M. Karplus, CHARMM: The Biomolecular Simulation Program. Journal of Computational Chemistry 30, 1545-1614 (2009).
- [15] A.D. MacKerell, D. Bashford, M. Bellott, R.L. Dunbrack, J. D. Evanseck, M.J. Field, S. Fischer, J. Gao, H. Guo, S. Ha, D. Joseph-McCarthy, L. Kuchnir, K. Kuczera, F.T. K. Lau, C. Mattos, S. Michnick, T. Ngo, D.T. Nguyen, B. Prodhom, W.E. Reiher, B. Roux, M. Schlenkrich, J.C. Smith, R. Stote, J. Straub, M. Watanabe, J. Wiorkiewicz-Kuczera, D. Yin, M. Karplus, All-Atom Empirical Potential for Molecular Modeling and Dynamics Studies of Proteins. Journal of Physical Chemistry B 102, 3586-3616 (1998).
- [16] A.D. Mackerell, Jr., M. Feig, C.L. Brooks, III, Improved Treatment of the Protein Backbone in Empirical Force Fields. J. Am. Chem. Soc. 126, 698-699 (2004).
- [17] M. Nina, D. Beglov, B. Roux, Atomic Radii for Continuum Electrostatics Calculations Based on Molecular Dynamics Free Energy Simulations. Journal of Physical Chemistry B 101, 5239-5248 (1997).
- [18] J. Ryckaert, G. Ciccotti, H.J.C. Berendsen, Numerical Integration of the Cartesian Equations of Motion of a System With Constraints: Molecular Dynamics of N-Alkanes. J. Comp. Phys. 23, 327-341 (1977).
- [19] D. Van der Spoel, E. Lindahl, B. Hess, G. Groenhof, A.E. Mark, H.J.C. Berendsen, GROMACS: Fast, Flexible, and Free. Journal of Computational Chemistry 26, 1701-1718 (2005).
- [20] J. Mongan, Interactive Essential Dynamics. Journal of Computer-Aided Molecular Design 18, 433-436 (2004).
- [21] W. Humphrey, A. Dalke, K. Schulten, VMD: Visual Molecular Dynamics, Journal of Molecular Graphics 14, 33-& (1996).
- [22] S. Haider, G.N. Parkinson, S. Neidle, Molecular Dynamics and Principal Components Analysis of Human Telomeric Quadruplex Multimers. Biophysical Journal 95, 296-311(2008).
- [23] S. Hayward, A. Kitao, H.J. Berendsen, Model-Free Methods of Analyzing Domain Motions in Proteins From Simulation: a Comparison of Normal Mode Analysis and Molecular Dynamics Simulation of Lysozyme. Proteins 27, 425-437 (1997).
- [24] S. Hayward, H.J. Berendsen, Systematic Analysis of Domain Motions in Proteins From Conformational Change: New Results on Citrat Synthase and T4 Lysozyme. Proteins 30, 144-154 (1998)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ5-0027-0088