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作 者:Dan Cheng Fan Jia Yun-Bao Jiang Vincent P.Conticello Tao Jiang
机构地区:[1]The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation,Department of Chemistry,College of Chemistry and Chemical Engineering,Xiamen University,Xiamen 361005,China [2]Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province(IKKEM),Xiamen 361005,China [3]Department of Chemistry,Emory University,Atlanta 30033,USA
出 处:《Nano Research》2024年第1期151-161,共11页纳米研究(英文版)
基 金:supported by the National Natural Science Foundation of China(Nos.22074128 and 22241503);Fundamental Research Funds for the Central Universities(Nos.20720210013 and 20720220005).
摘 要:Controlled peptide assembly offers significant promise to develop synthetic supramolecular nanostructures to display material and biological properties that mimic protein assemblies in nature.Despite the progress in forming peptide nanostructures of various morphology,there exists a distinct gap between natural and synthetic assembly systems in terms of size control.Constructing nanostructures with a narrow size distribution that can be tuned over a wide range of length-scales is essential for applications that require precise spacing between objects.This approach provides the opportunity to correlate materials and biological properties of interest with assembly size.In this review,we discuss representative endeavors over the past two decades for design of size-controllable peptide nanostructures using tunable building blocks.Other mechanisms for size control,e.g.,molecular frustration,template-directed peptide assembly,and multi-component peptide co-assembly,will also be discussed.We also demonstrate the applicable scopes of these strategies and suggest potential future avenues for scientific advances in this field.
关 键 词:peptide assembly controllable size TEMPLATE MULTI-COMPONENT
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