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Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature

Previous research suggests that carbohydrate mimetic peptide IF7 (IFLLWQR) has an excellent targeting property to annexin1 (Anxa1), a specific marker on the tumor endothelium. However, IF7 is susceptible to proteolysis and has a poor stability in vivo. We prepared a D-amino acid, reverse sequence pe...

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Detalles Bibliográficos
Autores principales: Chen, Xinyi, Fan, Zhuoyang, Chen, Yanzuo, Fang, Xiaoling, Sha, Xianyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846562/
https://www.ncbi.nlm.nih.gov/pubmed/24312470
http://dx.doi.org/10.1371/journal.pone.0080390
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author Chen, Xinyi
Fan, Zhuoyang
Chen, Yanzuo
Fang, Xiaoling
Sha, Xianyi
author_facet Chen, Xinyi
Fan, Zhuoyang
Chen, Yanzuo
Fang, Xiaoling
Sha, Xianyi
author_sort Chen, Xinyi
collection PubMed
description Previous research suggests that carbohydrate mimetic peptide IF7 (IFLLWQR) has an excellent targeting property to annexin1 (Anxa1), a specific marker on the tumor endothelium. However, IF7 is susceptible to proteolysis and has a poor stability in vivo. We prepared a D-amino acid, reverse sequence peptide of IF7, designated RIF7, to confer protease resistance while retaining bioactivity. Experimental results indicate that RIF7 had significantly increased stability and an increased receptor binding affinity than IF7, and this new moiety may represent a clinically relevant vehicle for anticancer drugs.
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spelling pubmed-38465622013-12-05 Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature Chen, Xinyi Fan, Zhuoyang Chen, Yanzuo Fang, Xiaoling Sha, Xianyi PLoS One Research Article Previous research suggests that carbohydrate mimetic peptide IF7 (IFLLWQR) has an excellent targeting property to annexin1 (Anxa1), a specific marker on the tumor endothelium. However, IF7 is susceptible to proteolysis and has a poor stability in vivo. We prepared a D-amino acid, reverse sequence peptide of IF7, designated RIF7, to confer protease resistance while retaining bioactivity. Experimental results indicate that RIF7 had significantly increased stability and an increased receptor binding affinity than IF7, and this new moiety may represent a clinically relevant vehicle for anticancer drugs. Public Library of Science 2013-12-02 /pmc/articles/PMC3846562/ /pubmed/24312470 http://dx.doi.org/10.1371/journal.pone.0080390 Text en © 2013 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chen, Xinyi
Fan, Zhuoyang
Chen, Yanzuo
Fang, Xiaoling
Sha, Xianyi
Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title_full Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title_fullStr Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title_full_unstemmed Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title_short Retro-Inverso Carbohydrate Mimetic Peptides with Annexin1-Binding Selectivity, Are Stable In Vivo, and Target Tumor Vasculature
title_sort retro-inverso carbohydrate mimetic peptides with annexin1-binding selectivity, are stable in vivo, and target tumor vasculature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846562/
https://www.ncbi.nlm.nih.gov/pubmed/24312470
http://dx.doi.org/10.1371/journal.pone.0080390
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