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“Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis

[Image: see text] We show that coating of decellularized extracellular matrix (DC-ECM) on substrate surfaces is an efficient way to generate a platform mimicking the native ECM environment. Moreover, the DC-ECM can be modified with a peptide (QK) mimicking vascular endothelial growth factor without...

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Detalles Bibliográficos
Autores principales: Wang, Lin, Zhao, Meirong, Li, Siheng, Erasquin, Uriel J., Wang, Hao, Ren, Li, Chen, Changyi, Wang, Yingjun, Cai, Chengzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059262/
https://www.ncbi.nlm.nih.gov/pubmed/24749832
http://dx.doi.org/10.1021/am501309d
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author Wang, Lin
Zhao, Meirong
Li, Siheng
Erasquin, Uriel J.
Wang, Hao
Ren, Li
Chen, Changyi
Wang, Yingjun
Cai, Chengzhi
author_facet Wang, Lin
Zhao, Meirong
Li, Siheng
Erasquin, Uriel J.
Wang, Hao
Ren, Li
Chen, Changyi
Wang, Yingjun
Cai, Chengzhi
author_sort Wang, Lin
collection PubMed
description [Image: see text] We show that coating of decellularized extracellular matrix (DC-ECM) on substrate surfaces is an efficient way to generate a platform mimicking the native ECM environment. Moreover, the DC-ECM can be modified with a peptide (QK) mimicking vascular endothelial growth factor without apparently compromising its integrity. The modification was achieved through metabolic incorporation of a “clickable” handle to DC-ECM followed by rapid attachment of the QK peptide with an azido tag using copper-catalyzed click reaction. The attachment of the QK peptide on to DC-ECM in this way further enhanced the angiogenic responses (formation of branched tubular networks) of endothelial cells.
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spelling pubmed-40592622015-04-21 “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis Wang, Lin Zhao, Meirong Li, Siheng Erasquin, Uriel J. Wang, Hao Ren, Li Chen, Changyi Wang, Yingjun Cai, Chengzhi ACS Appl Mater Interfaces [Image: see text] We show that coating of decellularized extracellular matrix (DC-ECM) on substrate surfaces is an efficient way to generate a platform mimicking the native ECM environment. Moreover, the DC-ECM can be modified with a peptide (QK) mimicking vascular endothelial growth factor without apparently compromising its integrity. The modification was achieved through metabolic incorporation of a “clickable” handle to DC-ECM followed by rapid attachment of the QK peptide with an azido tag using copper-catalyzed click reaction. The attachment of the QK peptide on to DC-ECM in this way further enhanced the angiogenic responses (formation of branched tubular networks) of endothelial cells. American Chemical Society 2014-04-21 2014-06-11 /pmc/articles/PMC4059262/ /pubmed/24749832 http://dx.doi.org/10.1021/am501309d Text en Copyright © 2014 American Chemical Society
spellingShingle Wang, Lin
Zhao, Meirong
Li, Siheng
Erasquin, Uriel J.
Wang, Hao
Ren, Li
Chen, Changyi
Wang, Yingjun
Cai, Chengzhi
“Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title_full “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title_fullStr “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title_full_unstemmed “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title_short “Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
title_sort “click” immobilization of a vegf-mimetic peptide on decellularized endothelial extracellular matrix to enhance angiogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059262/
https://www.ncbi.nlm.nih.gov/pubmed/24749832
http://dx.doi.org/10.1021/am501309d
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