The Molecular Foundry, Lawrence Berkeley National Laboratory , Berkeley, California 94720, United States.
J Am Chem Soc. 2018 Jan 31;140(4):1409-1414. doi: 10.1021/jacs.7b11005. Epub 2018 Jan 17.
Inspired by marine siderophores that exhibit a morphological shift upon metal coordination, hybrid peptide-polymer conjugates that assemble into different morphologies based on the nature of the metal ion coordination have been designed. Coupling of a peptide chelator, hexahistidine, with hydrophobic oligostyrene allows a modular strategy to be established for the efficient synthesis and purification of these tunable amphiphiles (oSt(His)). Remarkably, in the presence of different divalent transition metal ions (Mn, Co, Ni, Cu, Zn, and Cd) a variety of morphologies were observed. Zinc(II), cobalt(II), and copper(II) led to aggregated micelles. Nickel(II) and cadmium(II) produced micelles, and multilamellar vesicles were obtained in the presence of manganese(II). This work highlights the significant potential for transition metal ion coordination as a tool for directing the assembly of synthetic nanomaterials.
受海洋中的铁载体在与金属配位时表现出形态转变的启发,设计了基于金属离子配位性质而组装成不同形态的杂肽-聚合物缀合物。通过将肽螯合剂六组氨酸与疏水性低聚苯乙烯偶联,建立了一种用于高效合成和纯化这些可调谐两亲物(oSt(His))的模块化策略。值得注意的是,在存在不同的二价过渡金属离子(Mn、Co、Ni、Cu、Zn 和 Cd)时,观察到了多种形态。锌(II)、钴(II)和铜(II)导致聚集胶束。镍(II)和镉(II)生成胶束,而锰(II)存在时则得到了多层囊泡。这项工作突出了过渡金属离子配位作为指导合成纳米材料组装的工具的巨大潜力。