Hierarchical Assembly of Conductive Fibers from Coiled-Coil Peptide Building Blocks

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Adam Grosvirt-Dramen, Zachary J. Urbach, Paul J. Hurst, Claire E. Kwok, Joseph P. Patterson, Fengbin Wang and Allon I. Hochbaum*, 
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引用次数: 0

Abstract

Biology provides many sources of inspiration for synthetic and multifunctional nanomaterials. Naturally evolved proteins exhibit specialized, sequence-defined functions and self-assembly behavior. Recapitulating their molecularly defined self-assembly behavior, however, is challenging in de novo proteins. Peptides, on the other hand, represent a more well-defined and rationally designable space with the potential for sequence-programmable, stimuli-responsive design for structure and function, making them ideal building blocks of bioelectronic interfaces. In this work, we design peptides that exhibit stimuli-responsive self-assembly and the capacity to transport electrical current over micrometer-long distances. A lysine–lysine (KK) motif inserted at solvent-exposed positions of a coiled-coil-forming peptide sequence introduces pH-dependent control over a transition from unordered to α-helical peptide structure. The ordered state of the peptide serves as a building block for the assembly of coiled coils and higher-order assemblies. Cryo-EM structures of these structures reveal a hierarchical organization of α-helical peptides in a cross coiled coil (CCC) arrangement. Structural analysis also reveals a β-sheet fiber phase under certain conditions and placements of the KK motif, revealing a complex and sensitive self-assembly pathway. Both solid-state and solution-based electrochemical characterizations show that CCC fibers are electronically conductive. Single-fiber conductive AFM measurement indicates that the solid-state electrical conductivity is comparable with bacterial cytochrome filaments. Solution-deposited fiber films approximately doubled the electroactive surface area of the electrode, confirming their conductivity in aqueous environments. This work establishes a stimuli-responsive peptide sequence element for balancing the order–disorder transitions in peptides to control their self-assembly into highly organized electronically conductive nanofibers.

Abstract Image

从螺旋状缩氨酸构建块中分层组装导电纤维
生物学为合成和多功能纳米材料提供了许多灵感来源。自然进化的蛋白质表现出特殊的、序列定义的功能和自组装行为。然而,概括其分子定义的自组装行为在新生蛋白中是具有挑战性的。另一方面,多肽代表了一个更明确、更合理的可设计空间,具有序列可编程、结构和功能刺激响应设计的潜力,使其成为生物电子界面的理想构建块。在这项工作中,我们设计了具有刺激响应性自组装和传输电流微米长距离能力的肽。赖氨酸-赖氨酸(KK)基序插入到螺旋状肽序列的溶剂暴露位置,引入了从无序到α-螺旋肽结构过渡的ph依赖控制。肽的有序状态作为组装线圈和高阶组装的构建块。这些结构的低温电镜结构揭示了α-螺旋肽在交叉线圈(CCC)排列中的分层组织。结构分析还揭示了在一定条件和位置下KK基序的β-薄片纤维相,揭示了一个复杂而敏感的自组装途径。固态和溶液电化学表征表明,CCC纤维具有导电性。单纤维导电AFM测量表明固态电导率与细菌细胞色素丝相当。溶液沉积的纤维膜大约使电极的电活性表面积增加了一倍,证实了它们在水环境中的导电性。这项工作建立了一个刺激响应肽序列元件,用于平衡肽中的有序-无序过渡,以控制它们自组装成高度组织化的导电纳米纤维。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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