首页> 外文会议>International Conference on Processing amp; Manufacturing of Advanced Materials Pt.4; Jul 7-11, 2003; Leganes, Madrid, Spain >Polyrotaxanes: Challenge to Multivalent Binding with Biological Receptors on Cell Surfaces
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Polyrotaxanes: Challenge to Multivalent Binding with Biological Receptors on Cell Surfaces

机译:聚轮烷:挑战与细胞表面上的生物受体的多价结合。

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The challenge to multivalent binding between ligands and proteins or biological receptors on cell surfaces has been focused on using supramolecular-structured polymers, polyrotaxanes. Our designed polyrotaxanes consist of ligand-immobilized α-cyclodextrins (α-CDs) threaded onto a linear polymeric chain (polyethylene glydol) (PEG) capped both terminals with bulky end-groups via biodegradable linkages. Structural characteristics of these polyrotaxanes involve sliding and rotational motion of the ligands immobilized on α-CDs along a PEG chain as to easily face to binding sites on proteins, which can contribute much to enhanced multivalent binding with proteins.
机译:配体与蛋白质或细胞表面上的生物受体之间多价结合的挑战一直集中在使用超分子结构聚合物聚轮烷上。我们设计的聚轮烷由固定在线性聚合物链(聚乙二醇)(PEG)上的配体固定的α-环糊精(α-CD)组成,该链通过生物可降解的键合连接了两个末端带有庞大端基的末端。这些聚轮烷的结构特征涉及固定在α-CD上的配体沿着PEG链的滑动和旋转运动,从而易于面对蛋白质上的结合位点,这可以大大增强与蛋白质的多价结合。

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