超嗜热菌
酶
绿色荧光蛋白
蛋白质工程
化学
生物物理学
纳米技术
材料科学
生物化学
生物
大肠杆菌
基因
作者
Yusuke Azuma,Donald Hilvert
出处
期刊:Methods in molecular biology
日期:2018-01-01
卷期号:: 39-55
被引量:14
标识
DOI:10.1007/978-1-4939-7893-9_4
摘要
The packaging of active enzymes in protein cages is a powerful strategy to control catalytic activity. Using a positively supercharged variant of green fluorescent protein, GFP(+36), as a genetically programmable tag, enzymes can be rapidly and quantitatively loaded into an engineered variant of the Aquifex aeolicus cage-forming protein lumazine synthase (AaLS-13) that possesses a negatively charged lumen. The cargo is spontaneously localized within AaLS-13 cages by simply mixing the components in aqueous solution. This chapter describes a detailed protocol for the preparation of AaLS-13 cages and GFP(+36)-enzyme fusions, as well as characterization of the inclusion complexes. Suitable conditions for encapsulation and enzyme kinetic assays are also discussed.
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