The interaction of presl region of hepatitis B virus B-cell epitope antigen with specific hepatitis B neutralizing monoclonal antibody was examined by docking study. We modelled the 3D complex structure of B-cell epitope antigen residues CTTPAQGNSMFPSCCCTKPTDGNCY by homology modelling and docked it with die crystal structure of monoclonal antibody specific for the presl region of the hepatitis B virus. At the optimized docked conformation, the interactions between the amino acids of antigen and antibody were examined. It is found that the docked complex is stabilized by 59-3 kcal/mol. The stability of die docked antigen-antibody complex is due to hydrogen bonding and van der Waals interactions. The amino acids of the antigen and antibody responsible for the interaction were identified. © Indian Academy of Sciences.
CITATION STYLE
Rajkannan, R., & Malar, E. J. P. (2007). Docking of B-cell epitope antigen to specific hepatitis B antibody. In Journal of Chemical Sciences (Vol. 119, pp. 553–558). https://doi.org/10.1007/s12039-007-0069-6
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