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dc.contributor.advisorChing, Wai-Yimeng
dc.contributor.authorEifler, Jay Quinsoneng
dc.date.issued2014-07-17eng
dc.date.submitted2014 Springeng
dc.descriptionTitle from PDF of title page, viewed on July 16, 2014eng
dc.descriptionVitaeng
dc.descriptionThesis advisor: Wai-Yim Chingeng
dc.descriptionIncludes bibliographic references (pages 85-91)eng
dc.description.abstractIn bio-related research, large proteins are of important interest. We study two such proteins. Collagen contains one such protein, the collagen triple-helix, which forms part of the structural matrix for animals, such as in their bones and teeth. 1JS9 is another protein that is a component of the protein shell of the brome mosaic virus (BMV). And BMV is important for drug delivery and imaging. To better understand the properties of these proteins, quantum mechanically (QM) based results are needed, however computationally feasible methods are also necessary. The Orthogonalized Linear Combination of Atomic Orbitals (OLCAO) method is wellsuited for application to such large proteins. However, a new approach to reduce the computational cost and increase the computational feasibility is required and this extension to the method we call the Amino-Acid Based Method (AAPM) of OLCAO. In brief, the AAPM calculates electronic, self-consistent fi eld (scf) potentials for individual amino-acids with their neighboring amino-acids included as a boundary condition. This allows the costly scf part of the calculation to be skipped out. Additionally, the number of potentials used to describe the 1JS9 protein is also minimized. Results for e ective charge and bond order are obtained and analyzed for Collagen and preliminary eff ective charge results are obtained for 1JS9. The e ffective charge results of the AAPM represent well those already obtained with the scf OLCAO result, but with reduced cost and preserved accuracy. The bond order results for Collagen also represent well the hydrogen bonding based on bond distances observed in experimentally-dervied images between the individual chains of the collagen triple-helix as well as the observed hydrogen bonding networkeng
dc.description.tableofcontentsAbstract -- List of illustrations -- List of tables -- Acknowledgments -- Introduction -- Theoretical background -- Method -- Models for collagen and the amino acid potential method -- Collagen results -- Brome mosaic virus results -- Future work -- Initial input file for AAPM -- AAPM programs and potential reduction method -- Referenceseng
dc.format.extentxi, 92 pageseng
dc.identifier.urihttp://hdl.handle.net/10355/43496eng
dc.subject.otherThesis -- University of Missouri--Kansas City -- Physicseng
dc.titleApplication of ab initio calculations to collagen and brome mosaic viruseng
dc.typeThesiseng
thesis.degree.disciplinePhysics (UMKC)eng
thesis.degree.grantorUniversity of Missouri--Kansas Cityeng
thesis.degree.levelMasterseng
thesis.degree.nameM. S.eng


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