Abstract
The molecular mechanics/generalized Born surface area (MM/GBSA) method has been investigated with the aim of achieving a statistical precision of 1 kJ/mol for the results. We studied the binding of seven biotin analogues to avidin, taking advantage of the fact that the protein is a tetramer with four independent binding sites, which should give the same estimated binding affinities. We show that it is not enough to use a single long simulation (10 ns), because the standard error of such a calculation underestimates the difference between the four binding sites. Instead, it is better to run several independent simulations and average the results. With such an approach, we obtain the same results for the four binding sites, and any desired precision can be obtained by running a proper number of simulations. We discuss how the simulations should be performed to optimize the use of computer time. The correlation time between the MM/GBSA energies is βΌ5 ps and an equilibration time of 100 ps is needed. For MM/GBSA, we recommend a sampling time of 20β200 ps for each separate simulation, depending on the protein. With 200 ps production time, 5β50 separate simulations are required to reach a statistical precision of 1 kJ/mol (800β8000 energy calculations or 1.5β15 ns total simulation time per ligand) for the seven avidin ligands. This is an order of magnitude more than what is normally used, but such a number of simulations is needed to obtain statistically valid results for the MM/GBSA method. Β© 2009 Wiley Periodicals, Inc. J Comput Chem 2010