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Emergence by Design in Self-Assembling Protein Shells

机译:在自组装蛋白壳中的设计出现

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The use of proteins and peptides as nanoscale components to generate new-to-nature physical entities holds great promise in biocatalysis, therapeutic or diagnostic delivery, and materials templating. The majority of functionalized particles have been based on existing structures found in nature. Developing biomimetic particles in this way takes advantage of highly evolved platforms for organization or encapsulation of functional moieties, offering significant advantages in stoichiometry, multivalency, and sequestration. However, novel assembly paradigms for the modular construction of macromolecular structures are now greatly expanding the functional diversity of protein-based nanoparticles in health and manufacturing. In the February issue of ACS Nano, Kepiro et al. demonstrate the refinement of this concept, engineering the capacity for self-assembly such that it is integral to pore-forming peptide motifs, resulting in superior antibiotic activity of the self-assembled particle. Nature encodes multiple functions in proteins with exquisite efficiency, and emulating this multiplicity may be the ultimate goal of biomimetic nanotechnologies.
机译:使用蛋白质和肽作为纳米级组分产生新的物理实体,具有良好的生物催化,治疗或诊断递送和材料模板。大多数官能化颗粒基于本质上发现的现有结构。以这种方式开发仿生颗粒利用功能性部分的组织或封装的高度进化平台,在化学计量,多价和封存中提供了显着的优势。然而,新的组装范例用于模块化结构的大分子结构现在大大扩展了蛋白质的纳米粒子在健康和制造中的功能多样性。在2月份发行ACS Nano,Kepiro等人。证明了这种概念的改进,工程自组装的能力使得它与孔形成肽基序是一体的,导致自组装颗粒的优异抗生素活性。 Nature在蛋白质中用精致效率进行多种功能,并模拟这种多重性可能是仿生纳米技术的最终目标。

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