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Stabilization of α-helices by the self-assembly of macrocyclic peptides on the surface of gold nanoparticles for molecular recognition

机译:通过大环肽在金纳米颗粒表面自组装的分子分子识别来稳定α-螺旋

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摘要

A novel strategy to stabilize the α-helical secondary structures of peptides upon binding to gold nanoparticles is described. Using a model protein-protein interaction system, we showed that AuNPs decorated with stabilized p53 α-helix peptides can mediate specific molecular recognition with their target protein.
机译:描述了一种与金纳米颗粒结合后稳定肽的α-螺旋二级结构的新策略。使用模型蛋白质-蛋白质相互作用系统,我们显示了用稳定的p53α-螺旋肽修饰的AuNPs可以介导与其目标蛋白质的特异性分子识别。

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  • 来源
    《Chemical Communications》 |2013年第69期|7617-7619|共3页
  • 作者单位

    Translational Research Center for Protein Function Control, Yonsei University, Seoul 120-749, Korea,Department of Materials Science & Engineering, Yonsei University, Seoul 120-749, Korea;

    Translational Research Center for Protein Function Control, Yonsei University, Seoul 120-749, Korea,Department of Materials Science & Engineering, Yonsei University, Seoul 120-749, Korea;

    Translational Research Center for Protein Function Control, Yonsei University, Seoul 120-749, Korea,Department of Materials Science & Engineering, Yonsei University, Seoul 120-749, Korea;

    Translational Research Center for Protein Function Control, Yonsei University, Seoul 120-749, Korea,Department of Biotechnology, Yonsei University, Seoul 120-749, Korea;

    Translational Research Center for Protein Function Control, Yonsei University, Seoul 120-749, Korea,Department of Materials Science & Engineering, Yonsei University, Seoul 120-749, Korea;

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