a1 Department of Chemistry and Biochemistry, University of California, San Diego, CA, USA
a2 Department of Chemistry and Biochemistry, Department of Pharmacology, Howard Hughes Medical Institute, Chevy Chase, MD, USA
Molecular recognition plays a central role in biochemical processes. Although well studied, understanding the mechanisms of recognition is inherently difficult due to the range of potential interactions, the molecular rearrangement associated with binding, and the time and length scales involved. Computational methods have the potential for not only complementing experiments that have been performed, but also in guiding future ones through their predictive abilities. In this review, we discuss how molecular dynamics (MD) simulations may be used in advancing our understanding of the thermodynamics that drive biomolecular recognition. We begin with a brief review of the statistical mechanics that form a basis for these methods. This is followed by a description of some of the most commonly used methods: thermodynamic pathways employing alchemical transformations and potential of mean force calculations, along with end-point calculations for free energy differences, and harmonic and quasi-harmonic analysis for entropic calculations. Finally, a few of the fundamental findings that have resulted from these methods are discussed, such as the role of configurational entropy and solvent in intermolecular interactions, along with selected results of the model system T4 lysozyme to illustrate potential and current limitations of these methods.
c1 Author for correspondence: J. Wereszczynski, Department of Chemistry and Biochemistry, University of California, San Diego, CA, USA. Tel.: 858.822.0169; Fax: 858.534.4974; Email: email@example.com