生物分子
超分子化学
化学
纳米技术
笼子
主客化学
阳离子聚合
模板
分子识别
金属有机骨架
纳米结构
支柱
自组装
分子
吸附
晶体结构
结晶学
材料科学
有机化学
工程类
组合数学
结构工程
数学
作者
Ahmed Shaukat,Eduardo Anaya‐Plaza,Ngong Kodiah Beyeh,Mauri A. Kostiainen
标识
DOI:10.1002/chem.202104341
摘要
Supramolecular self-assembly of biomolecules provides a powerful bottom-up strategy to build functional nanostructures and materials. Among the different biomacromolecules, protein cages offer various advantages including uniform size, versatility, multi-modularity, and high stability. Additionally, protein cage crystals present confined microenvironments with well-defined dimensions. On the other hand, molecular hosts, such as cyclophanes, possess a defined cavity size and selective recognition of guest molecules. However, the successful combination of macrocycles and protein cages to achieve functional co-crystals has remained limited. In this study, we demonstrate electrostatic binding between cationic pillar[5]arenes and (apo)ferritin cages that results in porous and crystalline frameworks. The electrostatically assembled crystals present a face-centered cubic (FCC) lattice and have been characterized by means of small-angle X-ray scattering and cryo-TEM. These hierarchical structures result in a multiadsorbent framework capable of hosting both organic and inorganic pollutants, such as dyes and toxic metals, with potential application in water-remediation technologies.
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