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Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag

[Image: see text] We describe a novel epitope discovery strategy for creating an affinity agent/peptide tag pair. A synthetic polymer nanoparticle (NP) was used as the “bait” to catch an affinity peptide tag. Biotinylated peptide tag candidates of varied sequence and length were attached to an avidi...

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Autores principales: Yoshimatsu, Keiichi, Yamazaki, Tomohiko, Hoshino, Yu, Rose, Paul E., Epstein, Linda F., Miranda, Les P., Tagari, Philip, Beierle, John M., Yonamine, Yusuke, Shea, Kenneth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985795/
https://www.ncbi.nlm.nih.gov/pubmed/24410250
http://dx.doi.org/10.1021/ja410817p
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author Yoshimatsu, Keiichi
Yamazaki, Tomohiko
Hoshino, Yu
Rose, Paul E.
Epstein, Linda F.
Miranda, Les P.
Tagari, Philip
Beierle, John M.
Yonamine, Yusuke
Shea, Kenneth J.
author_facet Yoshimatsu, Keiichi
Yamazaki, Tomohiko
Hoshino, Yu
Rose, Paul E.
Epstein, Linda F.
Miranda, Les P.
Tagari, Philip
Beierle, John M.
Yonamine, Yusuke
Shea, Kenneth J.
author_sort Yoshimatsu, Keiichi
collection PubMed
description [Image: see text] We describe a novel epitope discovery strategy for creating an affinity agent/peptide tag pair. A synthetic polymer nanoparticle (NP) was used as the “bait” to catch an affinity peptide tag. Biotinylated peptide tag candidates of varied sequence and length were attached to an avidin platform and screened for affinity against the polymer NP. NP affinity for the avidin/peptide tag complexes was used to provide insight into factors that contribute NP/tag binding. The identified epitope sequence with an optimized length (tMel-tag) was fused to two recombinant proteins. The tagged proteins exhibited higher NP affinity than proteins without tags. The results establish that a fusion peptide tag consisting of optimized 15 amino acid residues can provide strong affinity to an abiotic polymer NP. The affinity and selectivity of NP/tMel-tag interactions were exploited for protein purification in conjunction with immobilized metal ion/His6-tag interactions to prepare highly purified recombinant proteins. This strategy makes available inexpensive, abiotic synthetic polymers as affinity agents for peptide tags and provides alternatives for important applications where more costly affinity agents are used.
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spelling pubmed-39857952015-01-10 Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag Yoshimatsu, Keiichi Yamazaki, Tomohiko Hoshino, Yu Rose, Paul E. Epstein, Linda F. Miranda, Les P. Tagari, Philip Beierle, John M. Yonamine, Yusuke Shea, Kenneth J. J Am Chem Soc [Image: see text] We describe a novel epitope discovery strategy for creating an affinity agent/peptide tag pair. A synthetic polymer nanoparticle (NP) was used as the “bait” to catch an affinity peptide tag. Biotinylated peptide tag candidates of varied sequence and length were attached to an avidin platform and screened for affinity against the polymer NP. NP affinity for the avidin/peptide tag complexes was used to provide insight into factors that contribute NP/tag binding. The identified epitope sequence with an optimized length (tMel-tag) was fused to two recombinant proteins. The tagged proteins exhibited higher NP affinity than proteins without tags. The results establish that a fusion peptide tag consisting of optimized 15 amino acid residues can provide strong affinity to an abiotic polymer NP. The affinity and selectivity of NP/tMel-tag interactions were exploited for protein purification in conjunction with immobilized metal ion/His6-tag interactions to prepare highly purified recombinant proteins. This strategy makes available inexpensive, abiotic synthetic polymers as affinity agents for peptide tags and provides alternatives for important applications where more costly affinity agents are used. American Chemical Society 2014-01-10 2014-01-29 /pmc/articles/PMC3985795/ /pubmed/24410250 http://dx.doi.org/10.1021/ja410817p Text en Copyright © 2014 American Chemical Society
spellingShingle Yoshimatsu, Keiichi
Yamazaki, Tomohiko
Hoshino, Yu
Rose, Paul E.
Epstein, Linda F.
Miranda, Les P.
Tagari, Philip
Beierle, John M.
Yonamine, Yusuke
Shea, Kenneth J.
Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title_full Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title_fullStr Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title_full_unstemmed Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title_short Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag
title_sort epitope discovery for a synthetic polymer nanoparticle: a new strategy for developing a peptide tag
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985795/
https://www.ncbi.nlm.nih.gov/pubmed/24410250
http://dx.doi.org/10.1021/ja410817p
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