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Structured Cyclic Peptides That Bind the EH Domain of EHD1

[Image: see text] EHD1 mediates long-loop recycling of many receptors by forming signaling complexes using its EH domain. We report the design and optimization of cyclic peptides as ligands for the EH domain of EHD1. We demonstrate that the improved affinity from cyclization allows fluorescence-base...

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Autores principales: Kamens, Alissa J., Eisert, Robyn J., Corlin, Tiffany, Baleja, James D., Kritzer, Joshua A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116148/
https://www.ncbi.nlm.nih.gov/pubmed/25014215
http://dx.doi.org/10.1021/bi500744q
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author Kamens, Alissa J.
Eisert, Robyn J.
Corlin, Tiffany
Baleja, James D.
Kritzer, Joshua A.
author_facet Kamens, Alissa J.
Eisert, Robyn J.
Corlin, Tiffany
Baleja, James D.
Kritzer, Joshua A.
author_sort Kamens, Alissa J.
collection PubMed
description [Image: see text] EHD1 mediates long-loop recycling of many receptors by forming signaling complexes using its EH domain. We report the design and optimization of cyclic peptides as ligands for the EH domain of EHD1. We demonstrate that the improved affinity from cyclization allows fluorescence-based screening applications for EH domain inhibitors. The cyclic peptide is also unusually well-structured in aqueous solution, as demonstrated using nuclear magnetic resonance-based structural models. Because few EH domain inhibitors have been described, these more potent inhibitors will improve our understanding of the roles of EHD1 in the context of cancer invasion and metastasis.
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spelling pubmed-41161482015-07-11 Structured Cyclic Peptides That Bind the EH Domain of EHD1 Kamens, Alissa J. Eisert, Robyn J. Corlin, Tiffany Baleja, James D. Kritzer, Joshua A. Biochemistry [Image: see text] EHD1 mediates long-loop recycling of many receptors by forming signaling complexes using its EH domain. We report the design and optimization of cyclic peptides as ligands for the EH domain of EHD1. We demonstrate that the improved affinity from cyclization allows fluorescence-based screening applications for EH domain inhibitors. The cyclic peptide is also unusually well-structured in aqueous solution, as demonstrated using nuclear magnetic resonance-based structural models. Because few EH domain inhibitors have been described, these more potent inhibitors will improve our understanding of the roles of EHD1 in the context of cancer invasion and metastasis. American Chemical Society 2014-07-11 2014-07-29 /pmc/articles/PMC4116148/ /pubmed/25014215 http://dx.doi.org/10.1021/bi500744q Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Kamens, Alissa J.
Eisert, Robyn J.
Corlin, Tiffany
Baleja, James D.
Kritzer, Joshua A.
Structured Cyclic Peptides That Bind the EH Domain of EHD1
title Structured Cyclic Peptides That Bind the EH Domain of EHD1
title_full Structured Cyclic Peptides That Bind the EH Domain of EHD1
title_fullStr Structured Cyclic Peptides That Bind the EH Domain of EHD1
title_full_unstemmed Structured Cyclic Peptides That Bind the EH Domain of EHD1
title_short Structured Cyclic Peptides That Bind the EH Domain of EHD1
title_sort structured cyclic peptides that bind the eh domain of ehd1
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116148/
https://www.ncbi.nlm.nih.gov/pubmed/25014215
http://dx.doi.org/10.1021/bi500744q
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