蛋白酶
融合蛋白
鼻病毒
烟草蚀刻病毒
重组DNA
生物化学
串联亲和纯化
半胱氨酸蛋白酶
酶
亲和层析
化学
分子生物学
生物
病毒
病毒学
马铃薯Y病毒
植物病毒
基因
作者
Elwy H. Abdelkader,Gottfried Otting
标识
DOI:10.1016/j.jbiotec.2020.11.005
摘要
The human rhinovirus 14 3C protease (HRV3C protease), in fusion with glutathione S-transferase also referred to as PreScission™ protease, is a cysteine protease of particular interest for affinity tag removal from fusion proteins due to its stringent recognition sequence specificity (LEVLFQ/GX) and superior activity at low temperature. Here we report the expression, purification and use of a fusion construct of HRV3C protease, NT*-HRV3CP, that affords high expression yield in E. coli (over 300 mg/L cell culture), facile single-step purification, high solubility (>10 mg/mL) and excellent storage properties. NT*-HRV3CP cleaves affinity tags at 4 °C in minutes, making it an attractive tool for the production of recombinant proteins for biotechnological, industrial and pharmaceutical applications.
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