Universal Optimizations of Scoring Functions for Virtual Screening
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- Onodera Kenji
- Institute of Industrial Science, University of Tokyo
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- Kamijo Shunsuke
- Institute of Industrial Science, University of Tokyo
Bibliographic Information
- Other Title
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- バーチャルスクリーニングのためのスコア関数の汎用的な最適化
Abstract
Structure-based virtual screening is gaining popularity in drug discovery. A number of molecular docking programs and scoring functions have been developed in the community, but they had not fulfilled the demands for the improved accuracy, yet. In order to improve the accuracy, the consensus scoring method has been developed. It combines docking scores from various scoring functions without considering characteristics of the docking scores. In this study, we adopted the concepts of the consensus scoring, and improved the docking score from each docking programs, DOCK, FRED or GOLD, for virtual screening. Instead using simple sum of score components in those docking scores, weight factors of the score components were introduced and adjusted for better predictions of active ligands during virtual screening. Several optimization processes were tested to find the best optimization methods of the docking scores using a wide variety of 113 target proteins with over 2000 diverse decoys. Finally, the optimizations improved the chance to discover the active ligands by up to 52.4% (e.g. from 36.8% to 56.1% using GOLD) for the test set. Additionally, the combination of the optimized scores using GOLD and FRED improved success rate in the test set by 77.2%, and approximately 70% of ligands for target proteins were predictable in the test set with 20 times enrichment.
Journal
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- Chem-Bio Informatics Journal
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Chem-Bio Informatics Journal 10 85-99, 2010
Chem-Bio Informatics Society
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Details 詳細情報について
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- CRID
- 1390282680081640448
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- NII Article ID
- 130004138115
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- ISSN
- 13470442
- 13476297
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed