摘要
N16蛋白具有抑制破骨和促进成骨作用,对骨质疏松疾病的治疗具有潜在的应用价值。采用pRHis质粒和BL21(DE3)plysS菌株,建立了表达产量较高的N16-pRHis-BL21(DE3)plysS表达体系;并建立了N16蛋白分离纯化工艺。该工艺表达方式简单,分离纯化操作简便,蛋白产量高,成本低,周期短,为进一步研究N16蛋白的功能奠定了基础。
N16 protein is a potential agent for treatment of osteoporosis due to its favorable anabolic and antiresorptive effects on bone. Our work described a biological engineering method to prepare N16. To build the high level expression system,pRHis plasmid was transformed into BL21( DE3) plys S strain.The present study has established a complete N16 preparation process with simple protein expression and purification procedures. This procedure can improve N16 protein production,reduce the cost and shorten the cycle,which will facilitate further studies on the functions of N16.
出处
《中山大学学报(自然科学版)》
CAS
CSCD
北大核心
2016年第3期135-138,144,共5页
Acta Scientiarum Naturalium Universitatis Sunyatseni
基金
深圳市科技研发资金资助项目(SGLH20120926171131592)
广东省海洋渔业科技推广专项资助项目(A201301C01)
广东省重大科技专项资助项目(2013A022100021)
关键词
N16蛋白
表达
纯化
制备工艺
N16 protein
expression
purification
preparation method