Towards Predictive Molecular Dynamics Simulations of DNA: Role of Electrostatics and of the Cell Environment.

Molecular Dynamics;5DNB;Electrostatics;1NAJ;DNA

Baucom, Jason Butler ; Celeste Sagui, Committee Chair,Christopher Roland, Committee Member,Carla Mattos, Committee Member,Steffen Heber, Committee Member,Baucom, Jason Butler ; Celeste Sagui ; Committee Chair ; Christopher Roland ; Committee Member ; Carla Mattos ; Committee Member ; Steffen Heber ; Committee Member

University:North Carolina State University

关键词: Molecular Dynamics;    5DNB;    Electrostatics;    1NAJ;    DNA;   

Others  :  https://repository.lib.ncsu.edu/bitstream/handle/1840.16/4433/etd.pdf?sequence=1&isAllowed=y

美国|英语

来源: null

【 摘 要 】

Molecular dynamics simulations of the DNA duplex d(CCAACGTTGG)2 were used to study the relationship between DNA sequence and structure in a crystal environment. Three different force fields were used: a traditional description based on atomic point charges, a polarizable force field, and an "extra-point" force field (with additional charges on extranuclear sites). It is found that all the force fields reproduce fairly well the sequence-dependent features of the experimental structure. The polarizable force field, however, provides the most accurate representation of the crystal structure and the sequence-dependent effects observed in the experiment. These results point out to the need of the inclusion of polarization for accurate descriptions of DNA. This work has also investigated to what extent molecular dynamics (MD) simulations can reproduce DNA sequence-specific features, given different electrostatic descriptions and different cell environments. For this purpose, we have carried out multiple unrestrained MD simulations of the DNA duplex d(CCAACGTTGG)2. With respect to the electrostatic descriptions, two different force fields are studied: a traditional description based on atomic point charges and a polarizable force field. With respect to the cell environment, the difference between crystal and solution environments is emphasized, as well as the structural importance of divalent ions. By imposing the correct experimental unit cell environment, an initial configuration with two ideal B-DNA duplexes in the unit cell, is shown to converge to the crystallographic structure. This convergence is measured by the appearance of sequence-dependent features that very closely resemble the crystallographic ones, as well as by the decay of the all-atom root-mean-squared coordinates deviations (RMSD) with respect to the crystallographic structure. Given the appropriate crystallographic constraints, this is first example of multiple nanosecond molecular dynamics trajectory that shows an ideal B-DNA model converging to an experimental structure, with a significant decay of RMSD. At later times, the polarizable force field is able to maintain this lower RMSD while the nonpolarizable force field starts to drift away.