超分子化学
单体
膜
聚合
聚合物
超分子聚合物
电荷(物理)
材料科学
自组装
化学物理
纳米技术
摩尔质量
肽
化学
神经突
阳离子聚合
高分子化学
芯(光纤)
结晶学
合成膜
分割
聚合度
订单(交换)
生物物理学
生物系统
作者
Michael D. Dore,Madison E. Strong,Simon A. Egner,Hiroaki Sai,Kyle J. Gray,Nozomu Takata,Alexie. Nyambi,Zhiwei Li,Liam C. Palmer,Samuel Isaac Stupp
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-10-01
卷期号:394 (6819): 125-132
标识
DOI:10.1126/science.aeg5583
摘要
Supramolecular polymers with precise micrometer-scale segments of opposite charge are challenging to synthesize as discrete assemblies in water. These systems could be used to pattern charged surfaces, interact with the membranes of cells, or form hierarchical structures. We report a living polymerization of fibrillar peptide assemblies with a central positively charged segment flanked by negative ones that can have a collective molar mass on the order of billions of daltons. The self-capping supramolecular polymerization required an untwisted β sheet core persisting along the entire length of the assembly as well as dormant ends in the absence of a monomer source. The positive domains of the segmented structures were anchored to the membranes of neurons, leaving the connected negative segments in a highly dynamic state near the cells through charge repulsion. The segmented architecture generated extensive neurite growth and synaptic activity.
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