Chemical Inducers of Dimerization for Profiling Protein Kinases
Chemical inducers of dimerization (CID) represent an important tool that has been implemented in numerous biological applications namely protein functions, protein stability, signal transduction, gene transcription, etc. Most generally CIDs are defined as bivalent molecules capable of inducing proxi...
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ndltd-arizona.edu-oai-arizona.openrepository.com-10150-5790192015-10-23T05:47:48Z Chemical Inducers of Dimerization for Profiling Protein Kinases Ogunleye, Olatokumbo Olajumi Luca Ghosh, Indraneel Ghosh, Indraneel Christie, Hamish Hruby, Victor Montfort, William kinase Chemistry Chemical inducer of dimerization Chemical inducers of dimerization (CID) represent an important tool that has been implemented in numerous biological applications namely protein functions, protein stability, signal transduction, gene transcription, etc. Most generally CIDs are defined as bivalent molecules capable of inducing proximity between two targeted proteins. This proximity can in turn promote or disfavor a certain biological activity. Cell permeable small molecules in particular represent a very effective method to induce precise temporal and spatial control over a specific biological target. Our lab has devoted much effort in studying and elucidating the activity and functions of protein kinases, which represent a very attractive therapeutic target for the treatment of cancer and many other disorders. Towards this goal we have developed a general CID enabled three-hybrid split-luciferase methodology for the investigation of kinase-inhibitor interactions in vitro. We demonstrate that by modulating the kinase-ligand affinity of the CID we are able to successfully profile many structurally non-related protein kinases. We also investigate the use of weaker affinity kinase ligands to allow competitive displacement of CID by the selected inhibitor. In addition we report the design, synthesis and applications of novel CID's for the profiling of kinase inhibitors in mammalian cells and we demonstrate the feasibility of the assay to be used as a new platform for the discovery of cell permeable kinase inhibitors. Finally, we report a new ligand-gated split-kinase that can be selectively activated by photocleavable inducers of dimerization. We further prove how the activity of split-proteins can be deactivated with temporal control with use of non DNA damaging UV radiation. 2015 text Electronic Dissertation http://hdl.handle.net/10150/579019 en_US Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. The University of Arizona. |
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en_US |
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kinase Chemistry Chemical inducer of dimerization |
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kinase Chemistry Chemical inducer of dimerization Ogunleye, Olatokumbo Olajumi Luca Chemical Inducers of Dimerization for Profiling Protein Kinases |
description |
Chemical inducers of dimerization (CID) represent an important tool that has been implemented in numerous biological applications namely protein functions, protein stability, signal transduction, gene transcription, etc. Most generally CIDs are defined as bivalent molecules capable of inducing proximity between two targeted proteins. This proximity can in turn promote or disfavor a certain biological activity. Cell permeable small molecules in particular represent a very effective method to induce precise temporal and spatial control over a specific biological target. Our lab has devoted much effort in studying and elucidating the activity and functions of protein kinases, which represent a very attractive therapeutic target for the treatment of cancer and many other disorders. Towards this goal we have developed a general CID enabled three-hybrid split-luciferase methodology for the investigation of kinase-inhibitor interactions in vitro. We demonstrate that by modulating the kinase-ligand affinity of the CID we are able to successfully profile many structurally non-related protein kinases. We also investigate the use of weaker affinity kinase ligands to allow competitive displacement of CID by the selected inhibitor. In addition we report the design, synthesis and applications of novel CID's for the profiling of kinase inhibitors in mammalian cells and we demonstrate the feasibility of the assay to be used as a new platform for the discovery of cell permeable kinase inhibitors. Finally, we report a new ligand-gated split-kinase that can be selectively activated by photocleavable inducers of dimerization. We further prove how the activity of split-proteins can be deactivated with temporal control with use of non DNA damaging UV radiation. |
author2 |
Ghosh, Indraneel |
author_facet |
Ghosh, Indraneel Ogunleye, Olatokumbo Olajumi Luca |
author |
Ogunleye, Olatokumbo Olajumi Luca |
author_sort |
Ogunleye, Olatokumbo Olajumi Luca |
title |
Chemical Inducers of Dimerization for Profiling Protein Kinases |
title_short |
Chemical Inducers of Dimerization for Profiling Protein Kinases |
title_full |
Chemical Inducers of Dimerization for Profiling Protein Kinases |
title_fullStr |
Chemical Inducers of Dimerization for Profiling Protein Kinases |
title_full_unstemmed |
Chemical Inducers of Dimerization for Profiling Protein Kinases |
title_sort |
chemical inducers of dimerization for profiling protein kinases |
publisher |
The University of Arizona. |
publishDate |
2015 |
url |
http://hdl.handle.net/10150/579019 |
work_keys_str_mv |
AT ogunleyeolatokumboolajumiluca chemicalinducersofdimerizationforprofilingproteinkinases |
_version_ |
1718109965917356032 |