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Protein Structural Analysis of Calbindin D28k Function and Dysregulation: Potential Competition Between Ca2+ and Zn2+

[ Vol. 13 , Issue. 7 ]


Sara Ibrahim Omar, Benedict C. Albensi and Kathleen M. Gough   Pages 777 - 786 ( 10 )


Calcium homeostasis is an essential physiological process requiring tight control in the normal cell. The dysregulation of calcium homeostasis may play a key role in the onset of Alzheimer’s disease (AD) and other disorders, whether through the loss of calcium binding or calcium sensing capacity. Calbindin D28k (CB-D28k), a calcium binding protein composed of six EF-hands, four of which can bind Ca2+, has been implicated in AD-related calcium dysregulation. In this study, docking and molecular dynamics calculations were employed to refine the protein data base model in order to understand the underlying structural variations between functional and non-functional EF-hands. Molecular modeling calculations improved the modelled protein structure: helix-loop-helix sequences were formed in all hands and most canonical interactions were formed in the four functional hands. The protein can also bind Zn2+, potentially altering the Ca2+ binding capability. Analysis of calculated structures of Zn2+ bound protein showed that only half of the correct EF-hand canonical interactions of Ca2+ were formed with loop residues. These results have important implications for the understanding of calcium dysregulation as well as for the development of novel therapeutic strategies in AD and other central nervous system disease processes, or in conditions of brain injury where calcium homeostasis is compromised.


Alzheimer's disease, Calbindin-D28k, Calcium binding protein, Calcium homeostasis, MD simulations, Zinc.


Department of Chemistry, Room 360 Parker Building, 144 Dysart Road, University of Manitoba, Winnipeg Manitoba, Canada R3T 2N2.

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