Literature DB >> 24777743

Modeling biophysical and biological properties from the characteristics of the molecular electron density, electron localization and delocalization matrices, and the electrostatic potential.

Chérif F Matta1.   

Abstract

The electron density and the electrostatic potential are fundamentally related to the molecular hamiltonian, and hence are the ultimate source of all properties in the ground- and excited-states. The advantages of using molecular descriptors derived from these fundamental scalar fields, both accessible from theory and from experiment, in the formulation of quantitative structure-to-activity and structure-to-property relationships, collectively abbreviated as QSAR, are discussed. A few such descriptors encode for a wide variety of properties including, for example, electronic transition energies, pK(a)'s, rates of ester hydrolysis, NMR chemical shifts, DNA dimers binding energies, π-stacking energies, toxicological indices, cytotoxicities, hepatotoxicities, carcinogenicities, partial molar volumes, partition coefficients (log P), hydrogen bond donor capacities, enzyme-substrate complementarities, bioisosterism, and regularities in the genetic code. Electronic fingerprinting from the topological analysis of the electron density is shown to be comparable and possibly superior to Hammett constants and can be used in conjunction with traditional bulk and liposolubility descriptors to accurately predict biological activities. A new class of descriptors obtained from the quantum theory of atoms in molecules' (QTAIM) localization and delocalization indices and bond properties, cast in matrix format, is shown to quantify transferability and molecular similarity meaningfully. Properties such as "interacting quantum atoms (IQA)" energies which are expressible into an interaction matrix of two body terms (and diagonal one body "self" terms, as IQA energies) can be used in the same manner. The proposed QSAR-type studies based on similarity distances derived from such matrix representatives of molecular structure necessitate extensive investigation before their utility is unequivocally established.
Copyright © 2014 The Authors Journal of Computational Chemistry Published by Wiley Periodicals, Inc.

Entities:  

Keywords:  QSAR; QTAIM; biophysical chemistry; electron density; physicochemical properties of molecules; quantitative structure-activity relationships; quantum theory of atoms in molecules

Mesh:

Substances:

Year:  2014        PMID: 24777743      PMCID: PMC4368384          DOI: 10.1002/jcc.23608

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


  89 in total

1.  Aspherical-atom scattering factors from molecular wave functions. 1. Transferability and conformation dependence of atomic electron densities of peptides within the multipole formalism.

Authors:  Tibor Koritsanszky; Anatoliy Volkov; Philip Coppens
Journal:  Acta Crystallogr A       Date:  2002-09-01       Impact factor: 2.290

2.  Atoms-in-molecules study of the genetically encoded amino acids. III. Bond and atomic properties and their correlations with experiment including mutation-induced changes in protein stability and genetic coding.

Authors:  Chérif F Matta; Richard F W Bader
Journal:  Proteins       Date:  2003-08-15

3.  Electron density distribution in stacked benzene dimers: a new approach towards the estimation of stacking interaction energies.

Authors:  Oleg A Zhikol; Oleg V Shishkin; Konstantin A Lyssenko; Jerzy Leszczynski
Journal:  J Chem Phys       Date:  2005-04-08       Impact factor: 3.488

4.  Integration of graph theory and quantum chemistry for structure-activity relationships.

Authors:  K Balasubramanian
Journal:  SAR QSAR Environ Res       Date:  1994       Impact factor: 3.000

5.  The bioisosteric similarity of the tetrazole and carboxylate anions: clues from the topologies of the electrostatic potential and of the electron density.

Authors:  Chérif F Matta; Alya A Arabi; Donald F Weaver
Journal:  Eur J Med Chem       Date:  2010-01-20       Impact factor: 6.514

6.  Effects of external electric fields on double proton transfer kinetics in the formic acid dimer.

Authors:  Alya A Arabi; Chérif F Matta
Journal:  Phys Chem Chem Phys       Date:  2011-07-01       Impact factor: 3.676

7.  Advances in understanding of chemical bonding: inputs from experimental and theoretical charge density analysis.

Authors:  Deepak Chopra
Journal:  J Phys Chem A       Date:  2012-09-07       Impact factor: 2.781

8.  Influences of solvent water on protein folding: free energies of solvation of cis and trans peptides are nearly identical.

Authors:  A Radzicka; L Pedersen; R Wolfenden
Journal:  Biochemistry       Date:  1988-06-14       Impact factor: 3.162

9.  Volumetric characterization of the hydration properties of heterocyclic bases and nucleosides.

Authors:  A Lee; T V Chalikian
Journal:  Biophys Chem       Date:  2001-09-18       Impact factor: 2.352

10.  Anomeric effect in halogenated methanols: a quantum theory of atoms in molecules study.

Authors:  David Ferro-Costas; Antonio Vila; Ricardo A Mosquera
Journal:  J Phys Chem A       Date:  2013-02-12       Impact factor: 2.781

View more
  18 in total

1.  Insights into the self-assembly steps of cyanuric acid toward rosette motifs: a DFT study.

Authors:  Andre N Petelski; Nélida M Peruchena; Silvana C Pamies; Gladis L Sosa
Journal:  J Mol Model       Date:  2017-08-14       Impact factor: 1.810

2.  Drug design by machine-trained elastic networks: predicting Ser/Thr-protein kinase inhibitors' activities.

Authors:  Cyrus Ahmadi Toussi; Javad Haddadnia; Chérif F Matta
Journal:  Mol Divers       Date:  2020-03-28       Impact factor: 2.943

3.  Classification models and SAR analysis on CysLT1 receptor antagonists using machine learning algorithms.

Authors:  Hongzhao Wang; Zijian Qin; Aixia Yan
Journal:  Mol Divers       Date:  2021-02-03       Impact factor: 3.364

4.  Surprising Conformers of the Biologically Important A·T DNA Base Pairs: QM/QTAIM Proofs.

Authors:  Ol'ha O Brovarets'; Kostiantyn S Tsiupa; Dmytro M Hovorun
Journal:  Front Chem       Date:  2018-02-27       Impact factor: 5.221

5.  Novel pathway for mutagenic tautomerization of classical А∙Т DNA base pairs via sequential proton transfer through quasi-orthogonal transition states: A QM/QTAIM investigation.

Authors:  Ol'ha O Brovarets'; Kostiantyn S Tsiupa; Dmytro M Hovorun
Journal:  PLoS One       Date:  2018-06-27       Impact factor: 3.240

6.  Unexpected Routes of the Mutagenic Tautomerization of the T Nucleobase in the Classical A·T DNA Base Pairs: A QM/QTAIM Comprehensive View.

Authors:  Ol'ha O Brovarets'; Kostiantyn S Tsiupa; Andrii Dinets; Dmytro M Hovorun
Journal:  Front Chem       Date:  2018-11-27       Impact factor: 5.221

7.  Revitalizing the concept of bond order through delocalization measures in real space.

Authors:  Carlos Outeiral; Mark A Vincent; Ángel Martín Pendás; Paul L A Popelier
Journal:  Chem Sci       Date:  2018-06-13       Impact factor: 9.825

Review 8.  Contributions of charge-density research to medicinal chemistry.

Authors:  Birger Dittrich; Chérif F Matta
Journal:  IUCrJ       Date:  2014-09-23       Impact factor: 4.769

9.  Non-dissociative structural transitions of the Watson-Crick and reverse Watson-Crick А·Т DNA base pairs into the Hoogsteen and reverse Hoogsteen forms.

Authors:  Ol'ha O Brovarets'; Kostiantyn S Tsiupa; Dmytro M Hovorun
Journal:  Sci Rep       Date:  2018-07-10       Impact factor: 4.379

10.  Novel Tautomerisation Mechanisms of the Biologically Important Conformers of the Reverse Löwdin, Hoogsteen, and Reverse Hoogsteen G*·C* DNA Base Pairs via Proton Transfer: A Quantum-Mechanical Survey.

Authors:  Ol'ha O Brovarets'; Timothy A Oliynyk; Dmytro M Hovorun
Journal:  Front Chem       Date:  2019-09-18       Impact factor: 5.221

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.