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用于控制纳米颗粒组装和生物传感的合成从头设计多肽。

Synthetic de novo designed polypeptides for control of nanoparticle assembly and biosensing.

作者信息

Aili D, Enander K, Baltzer L, Liedberg B

机构信息

Department of Physics, Biology and Chemistry, Linköping University, SE-581 83 Linköping, Sweden.

出版信息

Biochem Soc Trans. 2007 Jun;35(Pt 3):532-4. doi: 10.1042/BST0350532.

Abstract

This contribution describes how de novo designed synthetic helix-loop-helix polypeptides are utilized to control the assembly of gold nanoparticles and as scaffolds for biosensing. The synthetic polypeptides are designed to fold into a four-helix bundle upon dimerization. When immobilized on gold nanoparticles, dimerization and folding occur between peptides on neighbouring particles as an effect of particle aggregation and the folded polypeptides are rigid enough to keep the particles separated at a distance corresponding to the size of the four-helix bundle. Moreover, peptide dimerization offers a convenient route to assemble nanoparticles into hybrid multilayers on planar substrates. The drastic change in the resonance conditions of the localized nanoparticle surface plasmon upon particle aggregation is shown to be useful for optical detection of biomolecular interactions.

摘要

本论文描述了如何利用从头设计的合成螺旋-环-螺旋多肽来控制金纳米颗粒的组装,并将其作为生物传感的支架。合成多肽被设计成在二聚化时折叠成四螺旋束。当固定在金纳米颗粒上时,相邻颗粒上的肽之间会发生二聚化和折叠,这是颗粒聚集的结果,并且折叠后的多肽足够刚性,能够使颗粒以对应于四螺旋束大小的距离分开。此外,肽二聚化提供了一种将纳米颗粒组装成平面基底上的混合多层膜的便捷途径。研究表明,颗粒聚集时局部纳米颗粒表面等离子体共振条件的剧烈变化可用于生物分子相互作用的光学检测。

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