Efficient Expression of Acetylcholine-Binding Protein from Aplysia californica in Bac-to-Bac System

被引:6
|
作者
Lin, Bo [1 ]
Meng, Hailing [1 ]
Bing, Hui [1 ]
Zhangsun, Dongting [1 ]
Luo, Sulan [1 ]
机构
[1] Hainan Univ, Key Lab Marine Drug Haikou, Minist Educ, Key Lab Trop Biol Resources, Haikou 570228, Hainan, Peoples R China
基金
中国国家自然科学基金;
关键词
CRYSTAL-STRUCTURE; STRUCTURAL DETERMINANTS; ACHBP; RECEPTOR; REVEALS; COMPLEX; DESIGN; NACHR;
D O I
10.1155/2014/691480
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Bac-to-Bac baculovirus expression system can efficiently produce recombinant proteins, but the system may have to be optimized to achieve high-level expression for different candidate proteins. We reported here the efficient expression of acetylcholine-binding proteins from sea hares Aplysia californica (Ac-AChBP) and a convenient method to monitor protein expression level in this expression system. Three key factors affecting expression of Ac-AChBP were optimized for maximizing the yield, which included the cell density, volume of the infecting baculovirus inoculums, and the culturing time of postinfection. We have found it to reach a high yield of similar to 5mg/L, which needs 55 h incubation after infection at the cell density of 2 x 10(6) cells/mL with an inoculum volume ratio of 1 : 100. The optimized expression system in this study was also applied for expressing another protein Ls-AChBP from Lymnaea stagnalis successfully. Therefore, this established method is helpful to produce high yields of AChBP proteins for X-ray crystallographic structural and functional studies.
引用
收藏
页数:9
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