GFscore:: A general nonlinear consensus scoring function for high-throughput docking

被引:39
作者
Betzi, Stephane
Suhre, Karsten
Chetrit, Bernard
Guerlesquin, Francoise
Morelli, Xavier
机构
[1] IBSM, CNRS, UPR 9036, BIP Lab, F-13402 Marseille 20, France
[2] IBSM, IGS Lab, CNRS, UPR 2589,Struct & Genom Informat Lab, FR-13288 Marseille, France
关键词
D O I
10.1021/ci0600758
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Most of the recent published works in the field of docking and scoring protein/ligand complexes have focused on ranking true positives resulting from a Virtual Library Screening (VLS) through the use of a specified or consensus linear scoring function. In this work, we present a methodology to speed up the High Throughput Screening (HTS) process, by allowing focused screens or for hitlist triaging when a prohibitively large number of hits is identified in the primary screen, where we have extended the principle of consensus scoring in a nonlinear neural network manner. This led us to introduce a nonlinear Generalist scoring Function, GFscore, which was trained to discriminate true positives from false positives in a data set of diverse chemical compounds. This original Generalist scoring Function is a combination of the five scoring functions found in the CScore package from Tripos Inc. GFscore eliminates up to 75% of molecules, with a confidence rate of 90%. The final result is a Hit Enrichment in the list of molecules to investigate during a research campaign for biological active compounds where the remaining 25% of molecules would be sent to in vitro screening experiments. GFscore is therefore a powerful tool for the biologist, saving both time and money.
引用
收藏
页码:1704 / 1712
页数:9
相关论文
共 39 条
[1]   CASTp: Computed atlas of surface topography of proteins [J].
Binkowski, TA ;
Naghibzadeh, S ;
Liang, J .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3352-3355
[2]   Protein-based virtual screening of chemical databases. 1. Evaluation of different docking/scoring combinations [J].
Bissantz, C ;
Folkers, G ;
Rognan, D .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (25) :4759-4767
[3]   Prediction of interface residues in protein-protein complexes by a consensus neural network method: Test against NMR data [J].
Chen, HL ;
Zhou, HX .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2005, 61 (01) :21-35
[4]   Consensus scoring for ligand/protein interactions [J].
Clark, RD ;
Strizhev, A ;
Leonard, JM ;
Blake, JF ;
Matthew, JB .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2002, 20 (04) :281-295
[5]   STRATEGY FOR CHEMOTHERAPY OF INFECTIOUS-DISEASE [J].
COHEN, SS .
SCIENCE, 1977, 197 (4302) :431-432
[6]   The price of innovation: new estimates of drug development costs [J].
DiMasi, JA ;
Hansen, RW ;
Grabowski, HG .
JOURNAL OF HEALTH ECONOMICS, 2003, 22 (02) :151-185
[7]   Empirical scoring functions .1. The development of a fast empirical scoring function to estimate the binding affinity of ligands in receptor complexes [J].
Eldridge, MD ;
Murray, CW ;
Auton, TR ;
Paolini, GV ;
Mee, RP .
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 1997, 11 (05) :425-445
[8]   Fast calculation of molecular polar surface area as a sum of fragment-based contributions and its application to the prediction of drug transport properties [J].
Ertl, P ;
Rohde, B ;
Selzer, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (20) :3714-3717
[9]   Assessing scoring functions for protein-ligand interactions [J].
Ferrara, P ;
Gohlke, H ;
Price, DJ ;
Klebe, G ;
Brooks, CL .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (12) :3032-3047
[10]   ZINC - A free database of commercially available compounds for virtual screening [J].
Irwin, JJ ;
Shoichet, BK .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2005, 45 (01) :177-182