The entropic cost of protein-protein association: A case study on acetylcholinesterase binding to fasciculin-2

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Abstract

Protein-protein association is accompanied by a large reduction in translational and rotational (external) entropy, Based on a 15 ns molecular dynamics simulation of acetylcholinesterase (AChE) in complex with fasciculin 2 (Fas2), we estimate the loss in external entropy using quasiharmonic analysis and histogram-based approximations of the probability distribution function. The external entropy loss of AChE-Fas2 binding, ∼30 cal/mol K, is found to be significantly larger than most previously characterized protein-ligand systems. However, it is less than the entropy loss estimated in an earlier study by A. V. Finkelstein and J. Janin, which was based on atomic motions in crystals. © 2005 by the Biophysical Society.

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Minh, D. D. L., Bui, J. M., Chang, C. E., Jain, T., Swanson, J. M. J., & McCammon, J. A. (2005). The entropic cost of protein-protein association: A case study on acetylcholinesterase binding to fasciculin-2. Biophysical Journal, 89(4). https://doi.org/10.1529/biophysj.105.069336

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