BIOVIA DISCOVERY STUDIO ® 2018 COMPREHENSIVE MODELING AND SIMULATIONS FOR LIFE SCIENCES ACCURATELY PREDICT LIGAND BINDING ENERGIES Drug discovery is a multi-objective optimization. Drug discovery is a multi-objective optimization. Scientists have to optimize both biochemical potency and characteristics such as ADME and toxicity. The latest release of BIOVIA’s predictive science applica- tion, Discovery Studio ® , continues the evolution of new free energy prediction simulations. Built on BIOVIA Pipeline Pilot ™ , Discovery Studio ® is uniquely positioned as the most comprehensive, collaborative modeling and simulation application for Life Sciences discovery research.
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BIOVIA DISCOVERY STUDIO® 2018COMPREHENSIVE MODELING AND SIMULATIONS
FOR LIFE SCIENCES
ACCURATELY PREDICT LIGAND
BINDING ENERGIES
Drug discovery is a multi-objective optimization. Drug discovery is a multi-objective optimization. Scientists have to optimize both biochemical potency and characteristics such as ADME and toxicity. The latest release of BIOVIA’s predictive science applica-tion, Discovery Studio®, continues the evolution of new free energy prediction simulations. Built on BIOVIA Pipeline Pilot™, Discovery Studio® is uniquely positioned as the most comprehensive, collaborative modeling and simulation application for Life Sciences discovery research.
DISCOVERY STUDIO 2018Part of the 2018 BIOVIA product release series, Discovery Studio 2018 continues to deliver key new Small Molecule simulations and Antibody humanization enhancements.
NEW AND ENHANCED SCIENCE• New! Accurately predict relative ligand binding energy for a congeneric ligand series using the new free energy perturbation (FEP) method
- Pair Ligands for FEP: A new command to pair two ligands for a relative FEP calculation - Generate Ligand Pairs for FEP: A new protocol to plan a set of relative FEP calculations to span a dataset of congeneric ligands
- Set Up Relative FEP Calculations: A new protocol to gen-erate multiple simulation systems for performing FEP calculations - Free Energy Perturbation (FEP): A new protocol to run multiple FEP simulations in serial, parallel, or on grids using NAMD. This replaces the Free Energy Perturbation (NAMD™1) protocol in 2017 R2 that could only run a single system - Collate FEP Simulation Results: A new protocol to integrate and analyze results from multiple relative FEP simulations and calculate absolute free energy values
• New! Type molecules using CGenFF and charmm36 for CHARMm™ or NAMD1-based simulations with the MATCH™ typing engine from the Brooks Lab
• New! Predict stabilizing humanized residue mutations: Predict mutations to make an antibody more human-compatible with-out losing specificity of antigen binding
- Calculate Mutation Energy (Stability): An option has been added to allow mutations to be specified using a sequence alignment. This facilitates trialing large numbers of muta-tions, and is particularly useful in conjunction with the suggested mutation alignments created by the new Predict Humanizing Mutations protocol - A new Create Humanization Database example protocol has been created to process data for use in the Predict Human-izing Mutations protocol - The Prepare Germline Sources example protocol has been enhanced to optionally save each annotated gene sequence to a separate file. This allows a specific gene to be selected for use in the Predict Humanizing Mutations protocol
• New! CHARMM PBEQ ,4,5 Poisson-Boltzmann-based electro-static solver: The DelPhi electrostatics component has been replaced with a CHARMm PBEQ Solver, based on the CHARMm PBEQ module to solve the Poisson-Boltzmann equation. It includes a number of new features and improvements:
- A better definition of the Poisson-Boltzmann grid, based on the grid spacing and distance from boundary - An orthorhombic grid box to calculate the potential of mol-ecules more efficiently - The electrostatic potential values and energies are reported in kcal/mol.e and kcal/mol - The focusing center can be set up automatically as the center of a selected group of atoms, instead of the carte-sian coordinates - Calculations can now be performed for membrane environ-ments, either as a planar slab (uniform dielectric constant) or as multiple regions (cf. low dielectric hydrophobic region and lipid head group regions)
• Enhanced! Several of the pharmacophore protocols have been redesigned to improve performance and scalability for parallel computing, including:
Figure 1: Network map showing the relative similarities in a congeneric set of ligands.
Figure 2: Sequence hotspot map showing humanization hotspots according to germline analysis. At each position, detailed amino acid options are presented via ‘logo plots’.
hsp90_5
hsp90_4
hsp90_9
hsp90_3
hsp90_1
hsp90_2
hsp90_34
hsp90_40
hsp90_30hsp90_29
hsp90_18
hsp90_48
hsp90_51hsp90_12
hsp90_7
0.67
0.67
0.67
0.82
0.82
0.82
0.74
0.670.67
0.61
0.61
0.610.9
0.9
• New! A Post-Process Screen Library Results example protocol has been added to assist with post-processing large Screen Library results
• Update! TopKat® QMRF Reports6: All remaining extensible TopKat Toxicity Models QSAR Model Report Format (QMRF) reports have been accepted and published on the European Commission Joint Research Center (JRC)
QMRF # Title
Q17-33-0048 BIOVIA toxicity prediction model-acute fish toxicity
Q17-31-0047 BIOVIA toxicity prediction model-acute toxicity to Daphnia
Q17-44-0004BIOVIA toxicity prediction model-skin irritancy (mild vs moderate/severe)
Q17-44-0003 BIOVIA toxicity prediction model-skin irritancy (moderate vs severe)
Q17-44-0002 BIOVIA toxicity prediction model-skin irritancy (none vs irritant)
• Update! The TopKat Detailed Report now contains additional information to improve traceability and reproducibility
• Update! The Detailed Report in the Toxicity Prediction (Exten-sible) protocol has been modified to improve readability and interpretability
PARTNER SCIENCE• CHARMm: Incorporates the latest release of the academic
CHARMM, version c42b12
• NAMD: Distributed with the CPU edition, version 2.12• MODELER: Incorporates the latest release of the academic
MODELLER, version 9.197 • BLAST+: The BLAST+ version in Discovery Studio has been
updated to 2.7
DATABASES• ANTIBODY has been updated to include the latest antibody
template structures from the PDB (based on PDB release August 2017)
• BLAST databases updated for PDB_nr95, PDB, SwissProt, UniRef90, NR based on corresponding public databases as of March 2017
• The RCSB ligand database was updated for the RCSB Structure Search protocol (November 2017, 25,392 entries)
COMPATIBILITYDiscovery Studio 2018 is built on and supports the latest release of BIOVIA Pipeline Pilot, version 2018• 64-bit Support: Discovery Studio executables are now all
native 64-bit on both Linux and Windows
Figure 3: Comparison in CATALYST pharmacophore screening performance between DS2017 R2 and DS2018, of a 5-feature pharmacophore against a 50000-compound dataset.
Pharmacophore Mapping
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