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Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain
The vast majority of clinically approved protein kinase inhibitors target the ATP-binding pocket directly. Consequently, many inhibitors have broad selectivity profiles and most have significant off-target effects. Allosteric inhibitors are generally more selective, but are difficult to identify bec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967828/ https://www.ncbi.nlm.nih.gov/pubmed/27411893 http://dx.doi.org/10.1098/rsob.160089 |
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author | Burgess, Selena G. Oleksy, Arkadiusz Cavazza, Tommaso Richards, Mark W. Vernos, Isabelle Matthews, David Bayliss, Richard |
author_facet | Burgess, Selena G. Oleksy, Arkadiusz Cavazza, Tommaso Richards, Mark W. Vernos, Isabelle Matthews, David Bayliss, Richard |
author_sort | Burgess, Selena G. |
collection | PubMed |
description | The vast majority of clinically approved protein kinase inhibitors target the ATP-binding pocket directly. Consequently, many inhibitors have broad selectivity profiles and most have significant off-target effects. Allosteric inhibitors are generally more selective, but are difficult to identify because allosteric binding sites are often unknown or poorly characterized. Aurora-A is activated through binding of TPX2 to an allosteric site on the kinase catalytic domain, and this knowledge could be exploited to generate an inhibitor. Here, we generated an allosteric inhibitor of Aurora-A kinase based on a synthetic, vNAR single domain scaffold, vNAR-D01. Biochemical studies and a crystal structure of the Aurora-A/vNAR-D01 complex show that the vNAR domain overlaps with the TPX2 binding site. In contrast with the binding of TPX2, which stabilizes an active conformation of the kinase, binding of the vNAR domain stabilizes an inactive conformation, in which the αC-helix is distorted, the canonical Lys-Glu salt bridge is broken and the regulatory (R-) spine is disrupted by an additional hydrophobic side chain from the activation loop. These studies illustrate how single domain antibodies can be used to characterize the regulatory mechanisms of kinases and provide a rational basis for structure-guided design of allosteric Aurora-A kinase inhibitors. |
format | Online Article Text |
id | pubmed-4967828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-49678282016-08-04 Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain Burgess, Selena G. Oleksy, Arkadiusz Cavazza, Tommaso Richards, Mark W. Vernos, Isabelle Matthews, David Bayliss, Richard Open Biol Research The vast majority of clinically approved protein kinase inhibitors target the ATP-binding pocket directly. Consequently, many inhibitors have broad selectivity profiles and most have significant off-target effects. Allosteric inhibitors are generally more selective, but are difficult to identify because allosteric binding sites are often unknown or poorly characterized. Aurora-A is activated through binding of TPX2 to an allosteric site on the kinase catalytic domain, and this knowledge could be exploited to generate an inhibitor. Here, we generated an allosteric inhibitor of Aurora-A kinase based on a synthetic, vNAR single domain scaffold, vNAR-D01. Biochemical studies and a crystal structure of the Aurora-A/vNAR-D01 complex show that the vNAR domain overlaps with the TPX2 binding site. In contrast with the binding of TPX2, which stabilizes an active conformation of the kinase, binding of the vNAR domain stabilizes an inactive conformation, in which the αC-helix is distorted, the canonical Lys-Glu salt bridge is broken and the regulatory (R-) spine is disrupted by an additional hydrophobic side chain from the activation loop. These studies illustrate how single domain antibodies can be used to characterize the regulatory mechanisms of kinases and provide a rational basis for structure-guided design of allosteric Aurora-A kinase inhibitors. The Royal Society 2016-07-13 /pmc/articles/PMC4967828/ /pubmed/27411893 http://dx.doi.org/10.1098/rsob.160089 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Burgess, Selena G. Oleksy, Arkadiusz Cavazza, Tommaso Richards, Mark W. Vernos, Isabelle Matthews, David Bayliss, Richard Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title | Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title_full | Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title_fullStr | Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title_full_unstemmed | Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title_short | Allosteric inhibition of Aurora-A kinase by a synthetic vNAR domain |
title_sort | allosteric inhibition of aurora-a kinase by a synthetic vnar domain |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967828/ https://www.ncbi.nlm.nih.gov/pubmed/27411893 http://dx.doi.org/10.1098/rsob.160089 |
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