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Comparison of in vitro characteristics of a monomeric, dimeric and trimeric fibronectin-derived linear

https://repo.qst.go.jp/records/69864
https://repo.qst.go.jp/records/69864
ca80fc2e-16af-4180-9235-3a3ea42fba8a
Item type 会議発表用資料 / Presentation(1)
公開日 2009-09-29
タイトル
タイトル Comparison of in vitro characteristics of a monomeric, dimeric and trimeric fibronectin-derived linear
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_c94f
資源タイプ conference object
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 Jin, Zhao-Hui

× Jin, Zhao-Hui

WEKO 685887

Jin, Zhao-Hui

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Furukawa, Takako

× Furukawa, Takako

WEKO 685888

Furukawa, Takako

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Waki, Atsuo

× Waki, Atsuo

WEKO 685889

Waki, Atsuo

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Akaji, Kenichi

× Akaji, Kenichi

WEKO 685890

Akaji, Kenichi

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Coll, Jean-Luc

× Coll, Jean-Luc

WEKO 685891

Coll, Jean-Luc

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 685892

Saga, Tsuneo

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Fujibayashi, Yasuhisa

× Fujibayashi, Yasuhisa

WEKO 685893

Fujibayashi, Yasuhisa

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金 朝暉

× 金 朝暉

WEKO 685894

en 金 朝暉

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古川 高子

× 古川 高子

WEKO 685895

en 古川 高子

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佐賀 恒夫

× 佐賀 恒夫

WEKO 685896

en 佐賀 恒夫

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内容記述タイプ Abstract
内容記述 Multivalent interactions are frequently used to enhance ligand-receptor binding affinity. In this study a mono-, di- and trimeric AVTGRGDSY peptide derived from fibronectin were compared concerning the integrin receptor binding affinity and/or specificity. Methods: AVTGRGDSY monomer, dimer and trimer were synthesized, labeled with 125I or Cy5.5. Using human embryonic kidney cells HEK293 (naturally alphaV-positive and beta3-negative), HEK293(beta1) (beta1-transfected and alphaVbeta3-negative), HEK293(beta3)( beta3-transfected and strongly alphaVbeta3
-positive), and human glioblastoma cells U87MG (naturally alphaVbeta3-positive),
cell-binding assay, competitive inhibition assay, cell adhesion assay and confocal laser scanning microscopic study were performed to determine the bioactivities of these peptides. Results: The monomeric AVTGRGDSY showed specific binding to both HEK293(beta1) and HEK293(beta3) cells. Multimerization resulted in no change with HEK293 cells, diminished binding for HEK293(beta1) cells, but substantially enhanced binding for alphaVbeta3-positive HEK293(beta3) and U87MG cells in the presence of Mn2+. Moreover, the multimeric AVTGRGDSY peptides were found to be nearly comparable with th alphaVbeta3-specific cyclo(RGDfV) peptide in specificity and affinity for targeting alphaVbeta3 integrin. Conclusion: The multimeric AVTGRGDSY peptide might be an efficient alphaVbeta3-targeting molecule. The present study would be useful for better understanding of the molecular basis of the interaction between RGD ligands and integrin receptors.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 World Molecular Imaging Congress
発表年月日
日付 2009-09-26
日付タイプ Issued
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