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Rapid cross-linking of elastin-like polypeptides with (hydroxymethyl)phosphines in aqueous solution

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dc.contributor.authorLim, Dong Woo-
dc.contributor.authorNettles, Dana L.-
dc.contributor.authorSetton, Lori A.-
dc.contributor.authorChilkoti, Ashutosh-
dc.date.accessioned2021-06-23T19:41:22Z-
dc.date.available2021-06-23T19:41:22Z-
dc.date.created2021-01-21-
dc.date.issued2007-05-
dc.identifier.issn1525-7797-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/43761-
dc.description.abstractIn situ gelation of injectable polypeptide-based materials is attractive for minimally invasive in vivo implantation of biomaterials and tissue engineering scaffolds. We demonstrate that chemically cross-linked elastin-like polypeptide (ELP) hydrogels can be rapidly formed in aqueous solution by reacting lysine-containing ELPs with an organophosphorous cross-linker, beta-[tris(hydroxymethyl)phosphino]propionic acid (THPP) under physiological conditions. The mechanical properties of the cross-linked ELP hydrogels were largely modulated by the molar concentration of lysine residues in the ELP and the pH at which the cross-linking reaction was carried out. Fibroblasts embedded in ELP hydrogels survived the cross-linking process and were viable after in vitro culture for 3 days. DNA quantification of ELP hydrogels with encapsulated fibroblasts indicated that there was no significant difference in DNA content between day 0 and day 3 when ELP hydrogels were formed with an equimolar ratio of THPP and lysine residues of the ELPs. These results suggest that THPP cross-linking may be a biocompatible strategy for the in situ formation of cross-linked hydrogels.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleRapid cross-linking of elastin-like polypeptides with (hydroxymethyl)phosphines in aqueous solution-
dc.typeArticle-
dc.contributor.affiliatedAuthorLim, Dong Woo-
dc.identifier.doi10.1021/bm061059m-
dc.identifier.scopusid2-s2.0-34249867928-
dc.identifier.wosid000246413600013-
dc.identifier.bibliographicCitationBIOMACROMOLECULES, v.8, no.5, pp.1463 - 1470-
dc.relation.isPartOfBIOMACROMOLECULES-
dc.citation.titleBIOMACROMOLECULES-
dc.citation.volume8-
dc.citation.number5-
dc.citation.startPage1463-
dc.citation.endPage1470-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusPROTEIN-BASED POLYMERS-
dc.subject.keywordPlusINVERSE TEMPERATURE TRANSITION-
dc.subject.keywordPlusCARTILAGINOUS TISSUE-REPAIR-
dc.subject.keywordPlusTARGETED DRUG-DELIVERY-
dc.subject.keywordPlusMECHANICAL-BEHAVIOR-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusTHERMOPLASTIC ELASTOMERS-
dc.subject.keywordPlusRECOMBINANT PROTEINS-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/bm061059m-
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ERICA 공학대학 (DEPARTMENT OF BIONANO ENGINEERING)
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