DC Field | Value | Language |
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dc.contributor.author | Oh, EJ | - |
dc.contributor.author | Kim, JW | - |
dc.contributor.author | Kong, JH | - |
dc.contributor.author | Ryu, SH | - |
dc.contributor.author | Hahn, SK | - |
dc.date.accessioned | 2016-04-01T08:45:58Z | - |
dc.date.available | 2016-04-01T08:45:58Z | - |
dc.date.created | 2009-08-05 | - |
dc.date.issued | 2008-12 | - |
dc.identifier.issn | 1043-1802 | - |
dc.identifier.other | 2009-OAK-0000017262 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/28718 | - |
dc.description.abstract | Agonistic and antagonistic peptides for formyl peptide receptor like 1 (FPRL1) receptor have been investigated as novel drug candidates for inflammatory diseases such as sepsis, asthma, and rheumatoid arthritis. In this work, a novel protocol for the synthesis of hyaluronic acid (HA)-peptide (CWRYMVm) conjugate for FPRL1 receptor was successfully developed for further clinical applications of peptide drugs. Aminoethyl methacrylated HA (HA-AEMA) was synthesized by the coupling reaction of tetrabutyl ammonium salt of HA (HA-TBA) and AEMA using benzotriazol-1-yloxy-tris(dimethylamino) phosphonium hexafluorophosphate (BOP) in dimethyl sulfoxide (DMSO). Then, HA-AEMA was conjugated with CWRYMVm in water via Michael addition reaction between methacrylate group of HA-AEMA and thiol group in cysteine. The formation of HA-peptide conjugate was confirmed by H-1 NMR and gel permeation chromatography (GPC). The average number of conjugated peptide molecules could be controlled from 5 to 23 per single HA chain. The HA-peptide conjugate showed serum stability longer than four days. In vitro signal transduction activity of the HA-peptide conjugate for FPRL1 receptor was confirmed from the elevated levels of phospho-extracellular signal-regulated kinase (pERK) and calcium ion in FPRL1 overexpressing RBL-2H3 cells. The partially decreased biological activity of HA-peptide conjugates by the steric hindrance of HA was recovered after its degradation by hyaluronidase treatment. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.relation.isPartOf | BIOCONJUGATE CHEMISTRY | - |
dc.subject | SUSTAINED-RELEASE FORMULATION | - |
dc.subject | HYDROGELS | - |
dc.subject | DEGRADATION | - |
dc.subject | IDENTIFICATION | - |
dc.title | SIGNAL TRANSDUCTION OF HYALURONIC ACID-PEPTIDE CONJUGATE FOR FORMYL PEPTIDE RECEPTOR LIKE 1 RECEPTOR | - |
dc.type | Article | - |
dc.contributor.college | 생명과학과 | - |
dc.identifier.doi | 10.1021/BC800255Y | - |
dc.author.google | Oh, EJ | - |
dc.author.google | Kim, JW | - |
dc.author.google | Kong, JH | - |
dc.author.google | Ryu, SH | - |
dc.author.google | Hahn, SK | - |
dc.relation.volume | 19 | - |
dc.relation.issue | 12 | - |
dc.relation.startpage | 2401 | - |
dc.relation.lastpage | 2408 | - |
dc.contributor.id | 10069853 | - |
dc.relation.journal | BIOCONJUGATE CHEMISTRY | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | BIOCONJUGATE CHEMISTRY, v.19, no.12, pp.2401 - 2408 | - |
dc.identifier.wosid | 000261767800015 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 2408 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 2401 | - |
dc.citation.title | BIOCONJUGATE CHEMISTRY | - |
dc.citation.volume | 19 | - |
dc.contributor.affiliatedAuthor | Ryu, SH | - |
dc.contributor.affiliatedAuthor | Hahn, SK | - |
dc.identifier.scopusid | 2-s2.0-58149094924 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 28 | - |
dc.description.scptc | 15 | * |
dc.date.scptcdate | 2018-05-121 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | SUSTAINED-RELEASE FORMULATION | - |
dc.subject.keywordPlus | DEGRADATION | - |
dc.subject.keywordPlus | HYDROGELS | - |
dc.subject.keywordPlus | IDENTIFICATION | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
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