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Characterization of...
Characterization of interactions and pharmacophore development for DFG-out inhibitors to RET tyrosine kinase
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- Gao, Chunxia (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology
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- Grøtli, Morten, 1966 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology
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- Eriksson, Leif A, 1964 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology
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(creator_code:org_t)
- 2015-06-06
- 2015
- Engelska.
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Ingår i: Journal of Molecular Modeling. - : Springer Science and Business Media LLC. - 1610-2940 .- 0948-5023. ; 21:7
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Abstract
Ämnesord
Stäng
- RET (rearranged during transfection) tyrosine kinase is a promising target for several human cancers. Abt-348, Birb-796, Motesanib and Sorafenib are DFG-out multi-kinase inhibitors that have been reported to inhibit RET activity with good IC50 values. Although the DFG-out conformation has attracted great interest in the design of type II inhibitors, the structural requirements for binding to the RET DFG-out conformation remains unclear. Herein, the DFG-out conformation of RET was determined by homology modelling, the four inhibitors were docked, and the binding modes investigated by molecular dynamics simulation. Binding free energies were calculated using the molecular mechanics/Poisson-Bolzmann surface area (MM/PBSA) method. The trends in predicted binding free affinities correlated well with experimental data and were used to explain the activity difference of the studied inhibitors. Per-residue energy decomposition analyses provided further information on specific interaction properties. Finally, we also conducted a detailed e-pharmacophore modelling of the different RET-inhibitor complexes, explaining the common and specific pharmacophore features of the different complexes. The results reported herein will be useful in future rational design of novel DFG-out RET inhibitors.
Ämnesord
- NATURVETENSKAP -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
Nyckelord
- RET
- DFG-out inhibitors
- Molecular dynamics simulation
- MM-PB(GB)SA
- e-pharmacophore
- MEDULLARY-THYROID CANCER
- PARTICLE MESH EWALD
- MOLECULAR-MECHANICS
- FREE-ENERGIES
- BINDING-SITE
- FORCE-FIELD
- MODEL
- CONFORMATIONS
- DYNAMICS
- DESIGN
- Biochemistry & Molecular Biology
- Biophysics
- Chemistry
- Multidisciplinary
- Computer Science
- Interdisciplinary Applications
- ATES OF AMERICA
- V109
- P18281
- WAR MJS
- 1985
- JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- V107
- P3902
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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