Protein Engineering, Vol. 14, No. 10, 753-758,
October 2001
© 2001 Oxford University Press
Energetic analysis of binding of progesterone and 5ß-androstane-3,17-dione to anti-progesterone antibody DB3 using molecular dynamics and free energy calculations
Department of Chemistry, University of Kuopio, PO Box 1627, FIN-70211 Kuopio, Finland
Molecular dynamics simulations and molecular mechanics–Poisson–Boltzmann surface area (MM-PBSA) free energy calculations were used to study the energetics of the binding of progesterone (PRG) and 5ß-androstane-3,17-dione (5AD) to anti-PRG antibody DB3. Although the two steroids bind to DB3 in different orientations, their binding affinities are of the same magnitude, 1 nM for PRG and 8 nM for 5AD. The calculated relative binding free energy of the steroids, 8.8 kJ/mol, is in fair agreement with the experimental energy, 5.4 kJ/mol. In addition, computational alanine scanning was applied to study the role of selected amino acid residues of the ligand-binding site on the steroid cross-reactivity. The electrostatic and van der Waals components of the total binding free energies were found to favour more the binding of PRG, whereas solvation energies were more favourable for the binding of 5AD. The differences in the free energy components are due to the binding of the A rings of the steroids to different binding pockets: PRG is bound to a pocket in which electrostatic antibody–steroid interactions are dominating, whereas 5AD is bound to a pocket in which van der Waals and hydrophobic interactions dominate.