Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.
Biochemistry (Mosc). 2010 Jul;75(7):881-91. doi: 10.1134/s0006297910070102.
To elaborate a high-performance system for expression of genes of G-protein coupled receptors (GPCR), methods of direct and hybrid expression of 17 GPCR genes in Escherichia coli and selection of strains and bacteria cultivation conditions were investigated. It was established that expression of most of the target GPCR fused with the N-terminal fragment of OmpF or Mistic using media for autoinduction provides high output (up to 50 mg/liter).
为了阐述一个用于表达 G 蛋白偶联受体 (GPCR) 基因的高效系统,我们研究了在大肠杆菌中直接和混合表达 17 个 GPCR 基因的方法,以及菌株和细菌培养条件的选择。结果表明,使用自诱导培养基表达与 OmpF 或 Mistic 的 N 端片段融合的大多数目标 GPCR 可以提供高产量(高达 50mg/L)。