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具有遗传编码相互作用位点的分子蛋白衔接子指导等离子体活性纳米粒子结构的分级组装。

Molecular protein adaptor with genetically encoded interaction sites guiding the hierarchical assembly of plasmonically active nanoparticle architectures.

机构信息

Freiburg Institute for Advanced Studies (FRIAS), School of Soft Matter Research, University of Freiburg, Albertstrasse 19, Freiburg 79104, Germany.

Faculty of Biology, Schaenzlestrasse 1, Freiburg 79104, Germany.

出版信息

Nat Commun. 2015 Mar 27;6:6705. doi: 10.1038/ncomms7705.

Abstract

The control over the defined assembly of nano-objects with nm-precision is important to create systems and materials with enhanced properties, for example, metamaterials. In nature, the precise assembly of inorganic nano-objects with unique features, for example, magnetosomes, is accomplished by efficient and reliable recognition schemes involving protein effectors. Here we present a molecular approach using protein-based 'adaptors/connectors' with genetically encoded interaction sites to guide the assembly and functionality of different plasmonically active gold nanoparticle architectures (AuNP). The interaction of the defined geometricaly shaped protein adaptors with the AuNP induces the self-assembly of nanoarchitectures ranging from AuNP encapsulation to one-dimensional chain-like structures, complex networks and stars. Synthetic biology and bionanotechnology are applied to co-translationally encode unnatural amino acids as additional site-specific modification sites to generate functionalized biohybrid nanoarchitectures. This protein adaptor-based nano-object assembly approach might be expanded to other inorganic nano-objects creating biohybrid materials with unique electronic, photonic, plasmonic and magnetic properties.

摘要

利用基于蛋白质的“适配子/连接器”和具有遗传编码相互作用位点的方法,引导不同等离子体活性金纳米颗粒结构(AuNP)的组装和功能,实现对具有 nm 精度的纳米物体的定义组装的控制,对于创造具有增强性能的系统和材料(例如超材料)非常重要。在自然界中,通过涉及蛋白质效应物的高效且可靠的识别方案,实现了具有独特特性的无机纳米物体的精确组装,例如磁小体。本文提出了一种分子方法,

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