Full metadata record

DC Field Value Language
dc.contributor.authorPark, Subin-
dc.contributor.authorLee, Jangwook-
dc.contributor.authorJo, Mi-hee-
dc.contributor.authorNa, Jin Hee-
dc.contributor.authorPark, Sung-Gurl-
dc.contributor.authorJang, Hyeon-Ki-
dc.contributor.authorKang, Sun-Woong-
dc.contributor.authorKim, Jong-Ho-
dc.contributor.authorKim, Byung-Soo-
dc.contributor.authorPark, Jae Hyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorRyu, Ju Hee-
dc.contributor.authorKim, Kwangmeyung-
dc.date.accessioned2024-01-20T04:00:59Z-
dc.date.available2024-01-20T04:00:59Z-
dc.date.created2021-09-05-
dc.date.issued2016-07-
dc.identifier.issn0939-4451-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123897-
dc.description.abstractVascular endothelial growth factor receptor (VEGFR) and matrix metalloproteinase (MMP) are up-regulated in ischemic tissue and play pivotal roles in promoting angiogenesis. The purpose of the present study was to evaluate two fluorophore-conjugated peptide probes specific to VEGFR and MMP for dual-targeted in vivo monitoring of angiogenesis in a murine model of hindlimb ischemia. To this end, VEGFR-Probe and MMP-Probe were developed by conjugating distinct near-infrared fluorophores to VEGFR-binding and MMP substrate peptides, respectively. VEGFR-Probe exhibited specific binding to VEGFR on HUVECs, and self-quenched MMP-Probe produced strong fluorescence intensity in the presence of MMPs in vitro. Subsequently, VEGFR-Probe and MMP-Probe were successfully utilized for time course in vivo visualization of VEGFR or MMP, respectively. Simultaneous visualization provided information regarding the spatial distribution of these proteins, including areas of co-localization. This dual-targeted in vivo imaging approach will be useful for understanding the detailed mechanism of angiogenesis and for evaluating therapeutic angiogenesis.-
dc.languageEnglish-
dc.publisherSPRINGER WIEN-
dc.subjectGLYCOL CHITOSAN NANOPARTICLES-
dc.subjectENDOTHELIAL GROWTH-FACTOR-
dc.subjectMATRIX-METALLOPROTEINASE ACTIVITY-
dc.subjectVEGF RECEPTORS-
dc.subjectCANCER-THERAPY-
dc.subjectDIAGNOSIS-
dc.subjectTISSUE-
dc.subjectVASCULATURE-
dc.subjectDEGRADATION-
dc.subjectDYSFUNCTION-
dc.titleIn vivo monitoring of angiogenesis in a mouse hindlimb ischemia model using fluorescent peptide-based probes-
dc.typeArticle-
dc.identifier.doi10.1007/s00726-016-2225-0-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAMINO ACIDS, v.48, no.7, pp.1641 - 1654-
dc.citation.titleAMINO ACIDS-
dc.citation.volume48-
dc.citation.number7-
dc.citation.startPage1641-
dc.citation.endPage1654-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000377409900010-
dc.identifier.scopusid2-s2.0-84964374593-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeArticle-
dc.subject.keywordPlusGLYCOL CHITOSAN NANOPARTICLES-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusMATRIX-METALLOPROTEINASE ACTIVITY-
dc.subject.keywordPlusVEGF RECEPTORS-
dc.subject.keywordPlusCANCER-THERAPY-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusTISSUE-
dc.subject.keywordPlusVASCULATURE-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusDYSFUNCTION-
dc.subject.keywordAuthorVascular endothelial growth factor receptor-
dc.subject.keywordAuthorMatrix metalloproteinase-
dc.subject.keywordAuthorMolecular imaging-
dc.subject.keywordAuthorAngiogenesis-
dc.subject.keywordAuthorFluorescence imaging-
Appears in Collections:
KIST Article > 2016
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE