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源自β-肽折叠体自组装的趋磁分子结构。

Magnetotactic molecular architectures from self-assembly of β-peptide foldamers.

作者信息

Kwon Sunbum, Kim Beom Jin, Lim Hyung-Kyu, Kang Kyungtae, Yoo Sung Hyun, Gong Jintaek, Yoon Eunyoung, Lee Juno, Choi Insung S, Kim Hyungjun, Lee Hee-Seung

机构信息

Molecular-Level Interface Research Center, Department of Chemistry, KAIST, Daejeon 305-701, Korea.

Center for Cell-Encapsulation Research, Department of Chemistry, KAIST, Daejeon 305-701, Korea.

出版信息

Nat Commun. 2015 Oct 29;6:8747. doi: 10.1038/ncomms9747.

Abstract

The design of stimuli-responsive self-assembled molecular systems capable of undergoing mechanical work is one of the most important challenges in synthetic chemistry and materials science. Here we report that foldectures, that is, self-assembled molecular architectures of β-peptide foldamers, uniformly align with respect to an applied static magnetic field, and also show instantaneous orientational motion in a dynamic magnetic field. This response is explained by the amplified anisotropy of the diamagnetic susceptibilities as a result of the well-ordered molecular packing of the foldectures. In addition, the motions of foldectures at the microscale can be translated into magnetotactic behaviour at the macroscopic scale in a way reminiscent to that of magnetosomes in magnetotactic bacteria. This study will provide significant inspiration for designing the next generation of biocompatible peptide-based molecular machines with applications in biological systems.

摘要

设计能够进行机械功的刺激响应性自组装分子系统是合成化学和材料科学中最重要的挑战之一。在此,我们报道了折叠结构,即β-肽折叠体的自组装分子结构,相对于施加的静磁场会均匀排列,并且在动态磁场中还会表现出瞬时取向运动。这种响应可通过折叠结构中分子有序排列导致的抗磁磁化率放大各向异性来解释。此外,折叠结构在微观尺度上的运动可以转化为宏观尺度上的趋磁行为,其方式类似于趋磁细菌中的磁小体。这项研究将为设计下一代具有生物相容性的基于肽的分子机器并应用于生物系统提供重要的灵感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bb1/4640081/0bf921ac8da4/ncomms9747-f1.jpg

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