纳米颗粒
堆积
静电学
化学物理
肽
液晶
胶体
结晶学
分子动力学
表面电荷
六方晶系
静电
材料科学
粒子(生态学)
化学
电荷(物理)
航程(航空)
自组装
氨基酸
Crystal(编程语言)
晶体结构
纳米技术
化学工程
纳米结构
胶体晶体
粒径
生物矿化
静电相互作用
电荷
肽序列
作者
Yao Tang,Tianren Zhang,Dai-Bei Yang,Jacob Schwartz,Christopher J. Kloxin,Jeffery G. Saven,Darrin J. Pochan
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-02-05
卷期号:391 (6785): 604-610
标识
DOI:10.1126/science.adz6812
摘要
Programmable control of protein or colloidal nanoparticle self-assembly into targeted nanostructures, while maintaining stability across extreme pH conditions, remains a major challenge. We designed coiled-coil bundlemer peptide nanoparticles that form ordered, hierarchical materials across an unusually broad pH range (1, 7, and 14) dependent on patchy surface charge display. Nematic liquid crystal formation was observed at low concentration (~0.5 to 4 weight %) at pH 1 and pH 14, whereas higher concentration at pH 1 yielded hexagonal columnar phases. At neutral pH, the same patchy nanoparticles assembled into ordered lattices through electrostatic complexation. Molecular dynamics simulations revealed end-to-end particle stacking underlying all phases. Coiled coils with identical amino acid composition but lacking designed charge patches displayed no ordered assembly, demonstrating the importance of programmable electrostatic interactions with protein-like specificity of spatial display.
科研通智能强力驱动
Strongly Powered by AbleSci AI