Lin Bo, Meng Hailing, Bing Hui, Zhangsun Dongting, Luo Sulan
Key Laboratory of Tropical Biological Resources, Ministry of Education, Key Lab for Marine Drug of Haikou, Hainan University, Haikou, Hainan 570228, China.
Biomed Res Int. 2014;2014:691480. doi: 10.1155/2014/691480. Epub 2014 Jul 20.
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 ∼5 mg/L, which needs 55 h incubation after infection at the cell density of 2 × 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.
杆状病毒表达系统(Bac-to-Bac)能够高效生产重组蛋白,但针对不同的候选蛋白,该系统可能需要进行优化以实现高水平表达。我们在此报告了海兔(Aplysia californica)乙酰胆碱结合蛋白(Ac-AChBP)的高效表达以及在该表达系统中监测蛋白表达水平的便捷方法。为了使产量最大化,对影响Ac-AChBP表达的三个关键因素进行了优化,包括细胞密度、感染性杆状病毒接种物的体积以及感染后的培养时间。我们发现,在细胞密度为2×10⁶个细胞/mL、接种物体积比为1∶100的情况下,感染后经过55小时孵育,产量可高达约5 mg/L。本研究中优化的表达系统还成功用于表达来自椎实螺(Lymnaea stagnalis)的另一种蛋白Ls-AChBP。因此,这种已建立的方法有助于大量生产AChBP蛋白,用于X射线晶体学结构和功能研究。