Molecular Dynamic Simulations of Nucleosomes and Histone Tails: The Effects of Histone Variance and Post-Translational Modification

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dc.contributor.advisorPapoian, Gareginen_US
dc.contributor.authorWinogradoff, Daviden_US
dc.contributor.departmentChemical Physicsen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2016-02-06T06:33:34Z
dc.date.available2016-02-06T06:33:34Z
dc.date.issued2015en_US
dc.description.abstractThe packaging of genomic information and the regulation of gene expression are both fundamentally important to eukaryotic life. Meters of human DNA must fit inside the micron-diameter nucleus while still rapidly becoming available for templated processes such as transcription, replication, and repair. Therefore, the DNA-protein complex known as chromatin must dynamically transition between more compact, closed states and more accessible, open ones. To fully understand chromatin structure and dynamics, it is necessary to employ a multifaceted approach, integrating different general philosophies and scientific techniques that include experiment and computation. Since the DNA in chromatin is organized into arrays of nucleosomes, we take a bottom-up approach in this dissertation, striving first to understand the structure and dynamics of an individual nucleosome and subdomains thereof. Atomistic computational methods have provided useful tools to study DNA and protein dynamics at the nanosecond, and recently microsecond, timescale. In this dissertation, we present recent developments in the understanding of the nucleosome though atomistic molecular dynamics (MD) simulations. By applying different all-atom MD computational techniques, we demonstrate that replacing the canonical H3 histone with the centromere-specific variant CENP-A translates to greater structural flexibility in the nucleosome, that replacing H3 with CENP-A increases the plasticity of an individual histone dimer, and that the effects of acetylation on the H4 histone tail are cumulative and specific to lysine 16 mono-acetylation.en_US
dc.identifierhttps://doi.org/10.13016/M2WM66
dc.identifier.urihttp://hdl.handle.net/1903/17223
dc.language.isoenen_US
dc.subject.pqcontrolledBiophysicsen_US
dc.subject.pquncontrolledCENP-Aen_US
dc.subject.pquncontrolledCentromereen_US
dc.subject.pquncontrolledHistone tailsen_US
dc.subject.pquncontrolledHistone Variantsen_US
dc.subject.pquncontrolledMolecular Dynamicsen_US
dc.subject.pquncontrolledNucleosomesen_US
dc.titleMolecular Dynamic Simulations of Nucleosomes and Histone Tails: The Effects of Histone Variance and Post-Translational Modificationen_US
dc.typeDissertationen_US

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