Literature DB >> 12650590

Combining NMR spectral and structural data to form models of polychlorinated dibenzodioxins, dibenzofurans, and biphenyls binding to the AhR.

Richard D Beger1, Dan A Buzatu, Jon G Wilkes.   

Abstract

A three-dimensional quantitative spectrometric data-activity relationship (3D-QSDAR) modeling technique which uses NMR spectral and structural information that is combined in a 3D-connectivity matrix has been developed. A 3D-connectivity matrix was built by displaying all possible assigned carbon NMR chemical shifts, carbon-to-carbon connections, and distances between the carbons. Two-dimensional 13C-13C COSY and 2D slices from the distance dimension of the 3D-connectivity matrix were used to produce a relationship among the 2D spectral patterns for polychlorinated dibenzofurans, dibenzodioxins, and biphenyls (PCDFs, PCDDs, and PCBs respectively) binding to the aryl hydrocarbon receptor (AhR). We refer to this technique as comparative structural connectivity spectral analysis (CoSCoSA) modeling. All CoSCoSA models were developed using forward multiple linear regression analysis of the predicted 13C NMR structure-connectivity spectral bins. A CoSCoSA model for 26 PCDFs had an explained variance (r2) of 0.93 and an average leave-four-out cross-validated variance (q(2)4) of 0.89. A CoSCoSA model for 14 PCDDs produced an r2 of 0.90 and an average leave-two-out cross-validated variance (q(2)2) of 0.79. One CoSCoSA model for 12 PCBs gave an r2 of 0.91 and an average q(2)2 of 0.80. Another CoSCoSA model for all 52 compounds had an r2 of 0.85 and an average q(2)2 of 0.52. Major benefits of CoSCoSA modeling include ease of development since the technique does not use molecular docking routines.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12650590     DOI: 10.1023/a:1022479510524

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  22 in total

1.  Comparative structural connectivity spectra analysis (CoSCoSA) models of steroids binding to the aromatase enzyme.

Authors:  Richard D Beger; Jon G Wilkes
Journal:  J Mol Recognit       Date:  2002 May-Jun       Impact factor: 2.137

2.  Structures of apurinic and apyrimidinic sites in duplex DNAs.

Authors:  R D Beger; P H Bolton
Journal:  J Biol Chem       Date:  1998-06-19       Impact factor: 5.157

Review 3.  Comparative toxicology and mechanism of action of polychlorinated dibenzo-p-dioxins and dibenzofurans.

Authors:  S H Safe
Journal:  Annu Rev Pharmacol Toxicol       Date:  1986       Impact factor: 13.820

4.  Protein phi and psi dihedral restraints determined from multidimensional hypersurface correlations of backbone chemical shifts and their use in the determination of protein tertiary structures.

Authors:  R D Beger; P H Bolton
Journal:  J Biomol NMR       Date:  1997-09       Impact factor: 2.835

5.  Models of polychlorinated dibenzodioxins, dibenzofurans, and biphenyls binding affinity to the aryl hydrocarbon receptor developed using (13)c NMR data.

Authors:  R D Beger; J G Wilkes
Journal:  J Chem Inf Comput Sci       Date:  2001 Sep-Oct

6.  Polychlorinated dibenzofurans (PCDFs): effects of structure on binding to the 2,3,7,8-TCDD cytosolic receptor protein, AHH induction and toxicity.

Authors:  S Bandiera; T Sawyer; M Romkes; B Zmudzka; L Safe; G Mason; B Keys; S Safe
Journal:  Toxicology       Date:  1984-08       Impact factor: 4.221

Review 7.  Polychlorinated biphenyls (PCBs) and polybrominated biphenyls (PBBs): biochemistry, toxicology, and mechanism of action.

Authors:  S Safe
Journal:  Crit Rev Toxicol       Date:  1984       Impact factor: 5.635

8.  Binding of polychlorinated biphenyls classified as either phenobarbitone-, 3-methylcholanthrene- or mixed-type inducers to cytosolic Ah receptor.

Authors:  S Bandiera; S Safe; A B Okey
Journal:  Chem Biol Interact       Date:  1982-04       Impact factor: 5.192

9.  Polychlorinated dibenzo-p-dioxins: quantitative in vitro and in vivo structure-activity relationships.

Authors:  G Mason; K Farrell; B Keys; J Piskorska-Pliszczynska; L Safe; S Safe
Journal:  Toxicology       Date:  1986-10       Impact factor: 4.221

10.  A QSAR evaluation of Ah receptor binding of halogenated aromatic xenobiotics.

Authors:  O G Mekenyan; G D Veith; D J Call; G T Ankley
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

View more
  3 in total

1.  Complementary PLS and KNN algorithms for improved 3D-QSDAR consensus modeling of AhR binding.

Authors:  Svetoslav H Slavov; Bruce A Pearce; Dan A Buzatu; Jon G Wilkes; Richard D Beger
Journal:  J Cheminform       Date:  2013-11-21       Impact factor: 5.514

2.  Modeling chemical interaction profiles: II. Molecular docking, spectral data-activity relationship, and structure-activity relationship models for potent and weak inhibitors of cytochrome P450 CYP3A4 isozyme.

Authors:  Yunfeng Tie; Brooks McPhail; Huixiao Hong; Bruce A Pearce; Laura K Schnackenberg; Weigong Ge; Dan A Buzatu; Jon G Wilkes; James C Fuscoe; Weida Tong; Bruce A Fowler; Richard D Beger; Eugene Demchuk
Journal:  Molecules       Date:  2012-03-15       Impact factor: 4.411

3.  Modeling chemical interaction profiles: I. Spectral data-activity relationship and structure-activity relationship models for inhibitors and non-inhibitors of cytochrome P450 CYP3A4 and CYP2D6 isozymes.

Authors:  Brooks McPhail; Yunfeng Tie; Huixiao Hong; Bruce A Pearce; Laura K Schnackenberg; Weigong Ge; Luis G Valerio; James C Fuscoe; Weida Tong; Dan A Buzatu; Jon G Wilkes; Bruce A Fowler; Eugene Demchuk; Richard D Beger
Journal:  Molecules       Date:  2012-03-15       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.