纳米技术
材料科学
合理设计
纳米颗粒
药物输送
生物结合
蛋白质设计
蛋白质结构
化学
生物化学
作者
Bhuvana K. Shanbhag,Chang Liu,Pradeep G.C.,Tayyaba Younas,Kevin K.Y. Hu,Alex J. Fulcher,Weston B. Struwe,David L. Steer,Geoff Dumsday,Ian S. Harper,Philipp Kukura,Victoria S. Haritos,Lizhong He
标识
DOI:10.1002/adfm.202108039
摘要
Abstract Assembled protein particles, as emerging biomaterials, have broad applications ranging from vaccines and drug delivery to biocatalysis and particle tracking, but to date these require trial‐and‐error rational design experimentation and/or intensive computational methods to generate. Here, the authors describe an easy‐to‐implement engineering strategy to generate customized protein particles as multifunctional biomaterials. They utilize protein–peptide modules to generate functional nanoparticles whose assembly and size is controlled by the addition of mild stimuli. The protein assembling method is versatile, as exemplified through particle formation with 7 distinct protein modules, using a variety of assembly conditions tailored by the chemistries of 3 peptide partners. They have generated customized protein particles using enzymes, binding and reporter proteins, and their functions and utilities are demonstrated using biocatalysis, sensing, and labelling applications, respectively. Furthermore, co‐assembly with two functional proteins within one particle has been successfully achieved and demonstrated. Physical insights into the kinetics and molecular mechanisms of particle formation are revealed by small angle X‐ray scattering and mass photometry, providing fundamental knowledge to guide design and manufacture these interesting biomaterials in future. Their protein assembling strategy is a reliable method for fabricating a protein particle to deliver new functionalities on‐demand.
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