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Targeted free energy perturbation uses an invertible mapping to promote configuration space overlap and the convergence of free energy estimates. However, developing suitable mappings can be challenging. Wirnsberger et al. [J. Chem. Phys. 153, 144112 (2020)] demonstrated the use of machine learning to train deep neural networks that map between Boltzmann distributions for different thermodynamic states. Here, we adapt their approach to the free energy differences of a flexible bonded molecule, deca-alanine, with harmonic biases and different spring centers. When the neural network is trained until “early stopping”—when the loss value of the test set increases—we calculate accurate free energy differences between thermodynamic states with spring centers separated by 1 Å and sometimes 2 Å. For more distant thermodynamic states, the mapping does not produce structures representative of the target state, and the method does not reproduce reference calculations.