Literature DB >> 20968314

Binding energy landscape analysis helps to discriminate true hits from high-scoring decoys in virtual screening.

Dengguo Wei1, Hao Zheng, Naifang Su, Minghua Deng, Luhua Lai.   

Abstract

Although virtual screening through molecular docking has been widely applied in lead discovery, it is still challenging to distinguish true hits from high-scoring decoys because of the difficulty in accurately predicting protein-ligand binding affinities. Following the successful application of energy landscape analysis to both protein folding and biomolecular binding studies, we attempted to use protein-ligand binding energy landscape analysis to recognize true binders from high-scoring decoys. Two parameters describing the binding energy landscape were used for this purpose. The energy gap, defined as the difference between the binding energy of the native binding mode and the average binding energy of other binding modes in the "denatured binding phase", was used to describe the thermodynamic stability of binding, and the number of local binding wells in the landscapes was used to account for the kinetic accessibility. These parameters, together with the docking score, were combined using logistic regression to investigate their capability to discriminate true ligands from high-scoring decoys. Inhibitors and the noninhibitors of two enzyme systems, neuraminidase and cyclooxygenase-2, were used to test their discrimination capability. Using a five-fold cross-validation, the areas under the receiver operator characteristic curves (AUCs) from the best linear combinations of parameters reached 0.878 for neuraminidase and 0.776 for cyclooxygenase-2. To make a more independent test, inhibitors and high-scoring decoys in a directory of useful decoys (DUD), the largest and most comprehensive public data set for benchmarking virtual screen programs by far, were used as independent test sets to test the discrimination capability of these parameters. The AUCs of the best linear combinations of parameters for the independent test sets were 0.750 for neuraminidase and 0.855 for cyclooxygenase-2. Furthermore, combining these two parameters with the docking scoring function improved the enrichment ratio to 200-300% compared to that using the scoring function alone. This study suggests that incorporating information from binding energy landscape analysis can significantly increase the success rate of virtual screening.

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Year:  2010        PMID: 20968314     DOI: 10.1021/ci900463u

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  12 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-30       Impact factor: 11.205

Review 2.  Application of NMR and molecular docking in structure-based drug discovery.

Authors:  Jaime L Stark; Robert Powers
Journal:  Top Curr Chem       Date:  2012

3.  Prediction of ligand binding using an approach designed to accommodate diversity in protein-ligand interactions.

Authors:  Lorraine Marsh
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4.  Specificity quantification of biomolecular recognition and its implication for drug discovery.

Authors:  Zhiqiang Yan; Jin Wang
Journal:  Sci Rep       Date:  2012-03-12       Impact factor: 4.379

Review 5.  Structure-based virtual screening for drug discovery: a problem-centric review.

Authors:  Tiejun Cheng; Qingliang Li; Zhigang Zhou; Yanli Wang; Stephen H Bryant
Journal:  AAPS J       Date:  2012-01-27       Impact factor: 4.009

6.  A dynamic study of protein secretion and aggregation in the secretory pathway.

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Journal:  PLoS One       Date:  2014-10-03       Impact factor: 3.240

7.  Logistic Regression of Ligands of Chemotaxis Receptors Offers Clues about Their Recognition by Bacteria.

Authors:  Takashi Sagawa; Ryota Mashiko; Yusuke Yokota; Yasushi Naruse; Masato Okada; Hiroaki Kojima
Journal:  Front Bioeng Biotechnol       Date:  2018-01-22

Review 8.  Empirical Scoring Functions for Structure-Based Virtual Screening: Applications, Critical Aspects, and Challenges.

Authors:  Isabella A Guedes; Felipe S S Pereira; Laurent E Dardenne
Journal:  Front Pharmacol       Date:  2018-09-24       Impact factor: 5.810

9.  Can the energy gap in the protein-ligand binding energy landscape be used as a descriptor in virtual ligand screening?

Authors:  Arsen V Grigoryan; Hong Wang; Timothy J Cardozo
Journal:  PLoS One       Date:  2012-10-10       Impact factor: 3.240

10.  Ligand clouds around protein clouds: a scenario of ligand binding with intrinsically disordered proteins.

Authors:  Fan Jin; Chen Yu; Luhua Lai; Zhirong Liu
Journal:  PLoS Comput Biol       Date:  2013-10-03       Impact factor: 4.475

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