脚手架
支架蛋白
稳健性(进化)
纳米技术
表面改性
材料科学
合成生物学
可扩展性
计算机科学
蛋白质工程
计算生物学
化学
酶
生物
工程类
生物化学
机械工程
数据库
基因
信号转导
作者
R. Zhang,Sun-Young Kang,François Gaascht,Eliana L. Peña,Claudia Schmidt‐Dannert
标识
DOI:10.1101/2024.05.02.592261
摘要
ABSTRACT Inspired by the properties of natural protein-based biomaterials, protein nanomaterials are increasingly designed with natural or engineered peptides, or with protein building blocks. Very few examples describe the design of functional protein-based materials for biotechnological applications that can be readily manufactured, are amenable to functionalization, and exhibit robust assembly properties for macroscale material formation. Here, we designed a protein-scaffolding system that self-assembles into robust, macroscale materials suitable for cell-free applications. By controlling the co-expression in E. coli of self-assembling scaffold building blocks with and without modifications for covalent attachment of cross-linking cargo proteins, hybrid scaffolds with spatially organized conjugation sites are overproduced that can be readily isolated. Cargo proteins, including enzymes, are rapidly cross-linked onto scaffolds for the formation of functional materials. We show that these materials can be used for the cell-free operation of a co-immobilized two-enzyme reaction and that the protein material can be recovered and reused. We believe that this work will provide a versatile platform for the design and scalable production of functional materials with customizable properties and the robustness required for biotechnological applications.
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