Computational modeling of Ca2+ and Zn2+ competition in Calbindin D28k, implications for altering calcium homeostasis

dc.contributor.authorOmar, Sara
dc.contributor.examiningcommitteeAlbensi, Benedict (Pharmacology and Therapeutics) O'Neil, Joe (Chemistry) Schreckenbach, Georg (Chemistry)en_US
dc.contributor.supervisorGough, Kathleen (Chemistry)en_US
dc.date.accessioned2013-01-08T18:49:00Z
dc.date.available2013-01-08T18:49:00Z
dc.date.issued2013-01-08
dc.degree.disciplineChemistryen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractNeurodegeneration in Alzheimer's disease is characterised by multiple pathologies including disrupted calcium homeostasis and elevated Zn2+ levels. Calbindin D28k (CB-D28k), which buffers Ca2+ and can bind Zn2+, was suspected to be involved in these abnormalities. The PDB structure of this EF-hand protein shows that not all hands are well formed. Docking and molecular dynamics calculations were employed to achieve the two goals in this project. The first goal was to get a better structure of CB-D28k to improve our understanding of its behavior. Calculations improved the structure protein: helix-loop-helix sequences were formed in all hands and most canonical interactions were formed in the four functional hands. The second goal was to test the Ca2+ binding capacity of Zn2+-bound CB-D28k. Analysis of calculated structures showed that the Ca2+ binding capability of Zn2+ bound protein was significantly compromised, permitting only half of the correct canonical interactions with the loop residues.en_US
dc.description.noteFebruary 2013en_US
dc.identifier.urihttp://hdl.handle.net/1993/14425
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectCalbindin D28ken_US
dc.subjectZincen_US
dc.subjectCalciumen_US
dc.subjectComputational modelingen_US
dc.titleComputational modeling of Ca2+ and Zn2+ competition in Calbindin D28k, implications for altering calcium homeostasisen_US
dc.typemaster thesisen_US
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