Assemble-And-Match: A Novel Hybrid Tool for Enhancing Education and Research in Rational Structure Based Drug Design

被引:0
作者
Pouya Tavousi
Reza Amin
Sina Shahbazmohamadi
机构
[1] University of Connecticut,Department of Pharmaceutical Sciences
[2] University of Connecticut,Department of Mechanical Engineering
[3] University of Connecticut,Department of Biomedical Engineering
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Scientific Reports | / 8卷
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摘要
Rational drug design is the process of finding new medication that can activate or inhibit the biofunction of a target molecule by binding to it and forming a molecular complex. Here, shape and charge complementarities between drug and target are key. To help find effective drug molecules out of a huge pool of possibilities, physical and computer aided tools have been developed. Former offers a tangible experience of the molecular interactions yet lacks measurement and evaluation capabilities. Latter enables accurate and fast evaluations, but does not deliver the interactive tangible experience of physical models. We introduce a novel hybrid model called “Assemble-And-Match” where, we enhance and combine the unique features of the two categories. Assemble-And-Match works based on fabrication of customized molecular fragments using our developed software and a 3D printer. Fragments are hinged to each other in different combinations and form flexible peptide chains, conformable to tertiary structures, to fit in the binding pocket of a (3D printed) target molecule. Through embedded measurement marks, the molecular model is reconstructed in silico and its properties are evaluated. We expect Assemble-And-Match tool can enable combination of visuospatial perception with in silico computational power to aid research and education in drug design.
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[1]  
Todd A(2009)Rational drug design-identifying and characterising a target The pharmaceutical journal. 283 19-20
[2]  
Anderson R(2003)The process of structure-based drug design Chemistry & biology 10 787-797
[3]  
Groundwater PW(2004)Docking and scoring in virtual screening for drug discovery: methods and applications Nature reviews Drug discovery 3 935-949
[4]  
Anderson AC(1992)Calculation of the free energy of association for protein complexes Protein Science 1 169-181
[5]  
Kitchen DB(1995)Ligandprotein docking and rational drug design Current opinion in structural biology 5 224-228
[6]  
Decornez H(2002)Principles of docking: An overview of search algorithms and a guide to scoring functions Proteins: Structure, Function, and Bioinformatics 47 409-443
[7]  
Furr JR(1998)Empirical scoring functions. ii. the testing of an empirical scoring function for the prediction of ligand-receptor binding affinities and the use of bayesian regression to improve the quality of the model Journal of computer-aided molecular design 12 503-519
[8]  
Bajorath J(2011)Protein–ligand interaction energies with dispersion corrected density functional theory and high-level wave function based methods The Journal of Physical Chemistry A 115 11210-11220
[9]  
Horton N(2004)A quantum mechanics-based scoring function: study of zinc ion-mediated ligand binding Journal of the American Chemical Society 126 1020-1021
[10]  
Lewis M(2000)Knowledge-based scoring function to predict protein-ligand interactions Journal of molecular biology 295 337-356