Literature DB >> 11924734

Combined ab initio/empirical approach for optimization of Lennard-Jones parameters for polar-neutral compounds.

I Jen Chen1, Daxu Yin, Alexander D MacKerell.   

Abstract

The study of small functionalized organic molecules in aqueous solution is a useful step toward gaining a basic understanding of the behavior of biomolecular systems in their native aqueous environment. Interest in studying amines and fluorine-substituted compounds has risen from their intrinsic physicochemical properties and their prevalence in biological and pharmaceutical compounds. In the present study, a previously developed approach which optimizes Lennard-Jones (LJ) parameters via the use of rare gas atoms combined with the reproduction of experimental condensed phase properties was extended to polar-neutral compounds. Compounds studied included four amines (ammonia, methylamine, dimethylamine, and trimethylamine) and three fluoroethanes (1-fluoroethane, 1,1-difluoroethane, and 1,1,1-trifluoroethane). The resulting force field yielded heats of vaporization and molecular volumes in excellent agreement with the experiment, with average differences less than 1%. The current amine CHARMM parameters successfully reproduced experimental aqueous solvation data where methylamine is more hydrophilic than ammonia, with hydrophobicity increasing with additional methylation on the nitrogen. For both the amines and fluoroethanes the parabolic relationship of the extent of methylation or fluorination, respectively, to the heats of vaporization were reproduced by the new parameters. The present results are also discussed with respect to the impact of parameterization approach to molecular details obtained from computer simulations and to the unique biological properties of fluorine in pharmaceutical compounds.

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Year:  2002        PMID: 11924734     DOI: 10.1002/jcc.1166

Source DB:  PubMed          Journal:  J Comput Chem        ISSN: 0192-8651            Impact factor:   3.376


  25 in total

1.  Residue-specific side-chain packing determines the backbone dynamics of transmembrane model helices.

Authors:  Stefan Quint; Simon Widmaier; David Minde; Daniel Hornburg; Dieter Langosch; Christina Scharnagl
Journal:  Biophys J       Date:  2010-10-20       Impact factor: 4.033

Review 2.  Force fields for simulating the interaction of surfaces with biological molecules.

Authors:  Lewis Martin; Marcela M Bilek; Anthony S Weiss; Serdar Kuyucak
Journal:  Interface Focus       Date:  2016-02-06       Impact factor: 3.906

3.  Polarizable empirical force field for aromatic compounds based on the classical drude oscillator.

Authors:  Pedro E M Lopes; Guillaume Lamoureux; Benoît Roux; Alexander D Mackerell
Journal:  J Phys Chem B       Date:  2007-02-27       Impact factor: 2.991

4.  Drude polarizable force field for aliphatic ketones and aldehydes, and their associated acyclic carbohydrates.

Authors:  Meagan C Small; Asaminew H Aytenfisu; Fang-Yu Lin; Xibing He; Alexander D MacKerell
Journal:  J Comput Aided Mol Des       Date:  2017-02-11       Impact factor: 3.686

5.  Ammonium recruitment and ammonia transport by E. coli ammonia channel AmtB.

Authors:  Thomas P Nygaard; Carme Rovira; Günther H Peters; Morten Ø Jensen
Journal:  Biophys J       Date:  2006-09-29       Impact factor: 4.033

Review 6.  CHARMM additive and polarizable force fields for biophysics and computer-aided drug design.

Authors:  K Vanommeslaeghe; A D MacKerell
Journal:  Biochim Biophys Acta       Date:  2014-08-19

7.  Recent Developments and Applications of the CHARMM force fields.

Authors:  Xiao Zhu; Pedro E M Lopes; Alexander D Mackerell
Journal:  Wiley Interdiscip Rev Comput Mol Sci       Date:  2011-06-28

8.  Different transport behaviors of NH4 (+) and NH3 in transmembrane cyclic peptide nanotubes.

Authors:  Mingming Zhang; Jianfen Fan; Jian Xu; Peipei Weng; Huifang Lin
Journal:  J Mol Model       Date:  2016-09-06       Impact factor: 1.810

9.  Polarizable empirical force field for nitrogen-containing heteroaromatic compounds based on the classical Drude oscillator.

Authors:  Pedro E M Lopes; Guillaume Lamoureux; Alexander D Mackerell
Journal:  J Comput Chem       Date:  2009-09       Impact factor: 3.376

10.  CHARMM general force field: A force field for drug-like molecules compatible with the CHARMM all-atom additive biological force fields.

Authors:  K Vanommeslaeghe; E Hatcher; C Acharya; S Kundu; S Zhong; J Shim; E Darian; O Guvench; P Lopes; I Vorobyov; A D Mackerell
Journal:  J Comput Chem       Date:  2010-03       Impact factor: 3.376

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