纳米笼
纳米结构
蛋白质工程
纳米技术
肽
自组装
合成生物学
融合蛋白
蛋白质设计
材料科学
化学
蛋白质结构
计算生物学
生物
生物化学
重组DNA
基因
催化作用
酶
作者
Naoya Kobayashi,Ryoichi Arai
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 79-94
被引量:2
标识
DOI:10.1007/978-1-0716-3222-2_4
摘要
Protein cages and nanostructures are promising biocompatible medical materials, such as vaccines and drug carriers. Recent advances in designed protein nanocages and nanostructures have opened up cutting-edge applications in the fields of synthetic biology and biopharmaceuticals. A simple approach for constructing self-assembling protein nanocages and nanostructures is the design of a fusion protein composed of two different proteins forming symmetric oligomers. In this chapter, we describe the design and methods of protein nanobuilding blocks (PN-Blocks) using a dimeric de novo protein WA20 to construct self-assembling protein cages and nanostructures. A protein nanobuilding block (PN-Block), WA20-foldon, was developed by fusing an intermolecularly folded dimeric de novo protein WA20 and a trimeric foldon domain from bacteriophage T4 fibritin. The WA20-foldon self-assembled into several oligomeric nanoarchitectures in multiples of 6-mer. De novo extender protein nanobuilding blocks (ePN-Blocks) were also developed by fusing tandemly two WA20 with various linkers, to construct self-assembling cyclized and extended chain-like nanostructures. These PN-Blocks would be useful for the construction of self-assembling protein cages and nanostructures and their potential applications in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI