High-Sensitive Analysis of Oligopeptide-Induced Cell Penetration Using Phospholipid Polymer Nanoparticles Containing Quantum Dots

  • Goto Yusuke
    Department of Materials Engineering, The University of Tokyo
  • Matsuno Ryosuke
    Department of Materials Engineering, The University of Tokyo Center for NanoBio Integration (CNBI), The University of Tokyo
  • Konno Tomohiro
    Department of Materials Engineering, The University of Tokyo Center for NanoBio Integration (CNBI), The University of Tokyo
  • Takai Madoka
    Department of Materials Engineering, The University of Tokyo Center for NanoBio Integration (CNBI), The University of Tokyo
  • Ishihara Kazuhiko
    Department of Materials Engineering, The University of Tokyo Department of Bioengineering, The University of Tokyo Center for NanoBio Integration (CNBI), The University of Tokyo

抄録

We developed new polymer nanoparticles containing quantum dots with artificial cell membrane-biointerface as a highly sensitive bioimaging probe. These nanoparticles were prepared by assembling phospholipid polymer as a platform and oligopeptide as a bioaffinity moiety on the surface of the nanoparticles. They showed high resistance to non-specific cellular uptake from HeLa cells due to the nature of phospholipid polymer with phosphorylcholine groups. On the other hand, when arginine octapeptide was immobilized on their surface, they could permeate the membrane of HeLa cells effectively and good fluorescence based on quantum dots could be observed. Cytotoxicity and inflammation reaction were not produced by these nanoparticles even after immobilization of octapeptide. Thus we obtained stable fluorescent polymer nanoparticles covered with artificial cell membrane, which are useful as an excellent bioimaging probe evaluation for biomolecular function in the target cells.

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詳細情報 詳細情報について

  • CRID
    1390282680489785216
  • NII論文ID
    130005003954
  • DOI
    10.14723/tmrsj.34.189
  • COI
    1:CAS:528:DC%2BD1MXhtVOms7zO
  • ISSN
    21881650
    13823469
  • 本文言語コード
    ja
  • データソース種別
    • JaLC
    • Crossref
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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