成核
费斯特共振能量转移
肽
化学
离解(化学)
合理设计
静电学
动力学
自组装
纳米技术
单体
化学物理
分子
组合化学
生物物理学
材料科学
有机化学
物理化学
聚合物
生物化学
荧光
物理
生物
量子力学
作者
Wang Li,Yang Zhou,Xinran Zhang,Sheng He,Liulin Yang,Xiaoyu Cao,Zhong‐Qun Tian
标识
DOI:10.1021/acs.jpcb.4c05751
摘要
Nucleation is a critical step that determines the assembly pathway and the structure and functions of the peptide assemblies. However, the dynamic evolution of interactions between nucleating agents and peptides, as well as between peptides themselves during the nucleation process, remains elusive. Herein, we show that the heterogeneous nucleating agent carboxymethylcellulose (CMC) can promote the nucleation of Aβ16-20 (KF) peptide. The Förster resonance energy transfer (FRET) technology was used to unveil the interaction dynamics between the CMC and KF peptide. Initially, CMC enriches KF monomers through weak nondirectional electrostatic interactions. The electrostatic screening reduces the electrostatic repulsion between KF molecules. Subsequently, KF-KF interactions become dominant, leading to the dissociation of KF from the CMC and nucleation. By adjustment of the adding time, dosage, size, and active sites of CMC, the assembly kinetics of KF can be effectively controlled. This study helps gain a deep understanding of the early heterogeneous nucleation process of peptide assembly and provides valuable guidance for the rational design of efficient nucleating agents for peptide assembly toward functional materials.
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