首页> 外文期刊>Angewandte Chemie >Construction of Protein Nanowires through Cucurbit[8]uril-based Highly Specific Host-Guest Interactions: An Approach to the Assembly of Functional Proteins
【24h】

Construction of Protein Nanowires through Cucurbit[8]uril-based Highly Specific Host-Guest Interactions: An Approach to the Assembly of Functional Proteins

机译:通过基于葫芦[8]尿嘧啶的高特异性宿主-客体相互作用构建蛋白质纳米线:一种功能性蛋白质的组装方法。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Protein nanostructures are of great interest in the field of bionics, owing not only to their biocompatible and biodegradable properties, but also to their high structural durability, which facilitates recycling. Some creative strategies have been developed to construct protein nanostructures based on molecular recognition, such as symmetry, metal ion induction, or supramolecular interactions. Some protein nanostructures, such as artificial protein nanowires, protein rings, and protein spheres haye been created by these strategies and applied in catalysis, tissue imaging, diagnostics, and therapeutic treatments. Among them, host-guest supramolecular interactions have provided desirable driving forces in a reversible and bioorthogonal manner. Although host-guest interactions have been successfully developed using protein-ligand interactions, such as biotin-streptavidin,dihydro-folate reductase-methotrexate,and lectin concanavalin A-mannopyranoside, the construction of functional protein nanostructures by small molecule host-guest interactions has rarely been explored.
机译:蛋白质纳米结构不仅在生物仿生领域具有生物相容性和可生物降解性,而且由于其高结构耐久性(有利于回收利用)而在仿生学领域引起了广泛关注。已经开发出一些创新的策略来构建基于分子识别的蛋白质纳米结构,例如对称性,金属离子诱导或超分子相互作用。这些策略创建了一些蛋白质纳米结构,例如人造蛋白质纳米线,蛋白质环和蛋白质球,并应用于催化,组织成像,诊断和治疗。其中,宿主-客体超分子相互作用以可逆的和生物正交的方式提供了所需的驱动力。尽管已经使用蛋白质-配体相互作用成功开发了宿主-客体相互作用,例如生物素-链霉亲和素,二氢叶酸还原酶-甲氨蝶呤和凝集素伴刀豆球蛋白A-甘露吡喃糖苷,但通过小分子宿主-客体相互作用构建功能性蛋白质纳米结构的情况很少被探索了。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号