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Synthesis and Biological Characterisation of Targeted Pro-Apoptotic Peptide
https://repo.qst.go.jp/records/45479
https://repo.qst.go.jp/records/454797c0577e6-6bfb-457e-98fa-ac1151eae9c9
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2009-04-15 | |||||
タイトル | ||||||
タイトル | Synthesis and Biological Characterisation of Targeted Pro-Apoptotic Peptide | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Foillard, Stephanie
× Foillard, Stephanie× Jin, Zhao-Hui× et.al× 金 朝暉 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | We report herein the synthesis and in vitro assay of new, multimeric RGD-peptide conjugates for cell-targeted drug delivery. We generated a peptide scaffold comprising two functional domains, one a tumour blood vessel homing motif and the other a programmed cell-death-inducing peptide sequence. RGD peptides were selected to direct the molecular conjugate to V 3 integrin-containing tumour cells. The pro-apoptotic (Lys-Leu-Ala-Lys-Leu-Ala-Lys)2 peptide was found to be nontoxic outside cells, but toxic when internalized into targeted cells as it disrupted the mitochondrial membrane. The synthesis of these targeted pro-apoptotic conjugates was carried out by assembling three different units (that is, scaffold, RGD units and pro-apoptotic peptide) through chemoselective ligations. We show that one compound displays significant biological effect in V 3 integrin-containing tumour cells. | |||||
書誌情報 |
Chembiochem 巻 9, 号 14, p. 2326-2332, 発行日 2008-08 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1439-4227 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1002/cbic.200800327 |