Boyce Thompson Institute at Cornell University, Ithaca, NY 14853, USA.
BMC Biotechnol. 2010 Jul 5;10:50. doi: 10.1186/1472-6750-10-50.
The insect cell line is a critical component in the production of recombinant proteins in the baculovirus expression system and new cell lines hold the promise of increasing both quantity and quality of protein production.
Seventy cell lines were established by single-cell cloning from a primary culture of cells derived from eggs of the black witch moth (Ascalapha odorata; Lepidoptera, Noctuidae). Among 8 rapidly growing lines, cell line 38 (Ao38) was selected for further analysis, based on susceptibility to AcMNPV infection and production of secreted alkaline phosphatase (SEAP) from a baculovirus expression vector. In comparisons with low-passage High Five (BTI-Tn-5B1-4) cells, infected Ao38 cells produced beta-galactosidase and SEAP at levels higher (153% and 150%, respectively) than those measured from High Five cells. Analysis of N-glycans of SEAP produced in Ao38 cells revealed two N-glycosylation sites and glycosylation patterns similar to those reported for High Five and Sf9 cells. Glycopeptide isoforms consisted of pauci- or oligomannose, with and without fucose on N-acetylglucosamine(s) linked to asparagine residues. Estimates of Ao38 cell volume suggest that Ao38 cells are approximately 2.5x larger than Sf9 cells but only approximately 74% of the size of High Five cells. Ao38 cells were highly susceptible to AcMNPV infection, similar to infectivity of Sf9 cells. Production of infectious AcMNPV budded virions from Ao38 cells peaked at approximately 4.5 x 10(7) IU/ml, exceeding that from High Five cells while lower than that from Sf9 cells. Ao38 cells grew rapidly in stationary culture with a population doubling time of 20.2 hr, and Ao38 cells were readily adapted to serum-free medium (Sf-900III) and to a suspension culture system. Analysis of Ao38 and a parental Ascalapha odorata cell line indicated that these lines were free of the alphanodavirus that was recently identified as an adventitious agent in High Five cell lines.
Ao38 cells represent a highly productive new insect cell line that will be useful for heterologous protein expression and other applications in biotechnology.
昆虫细胞系是杆状病毒表达系统中重组蛋白生产的关键组成部分,新的细胞系有望提高蛋白生产的数量和质量。
从黑女巫蛾(Ascalapha odorata;鳞翅目,夜蛾科)的原代细胞培养物中通过单细胞克隆建立了 70 个细胞系。在 8 个快速生长的细胞系中,基于对 AcMNPV 感染的敏感性和杆状病毒表达载体分泌碱性磷酸酶(SEAP)的产生,选择了第 38 号细胞系(Ao38)进行进一步分析。与低传代 High Five(BTI-Tn-5B1-4)细胞相比,感染的 Ao38 细胞产生的β-半乳糖苷酶和 SEAP 的水平分别高于 High Five 细胞(分别为 153%和 150%)。对 Ao38 细胞中产生的 SEAP 的 N-糖链分析表明,存在两个 N-糖基化位点,糖基化模式与 High Five 和 Sf9 细胞报道的相似。糖肽同工型由低聚甘露糖或寡甘露糖组成,有或没有连接到天冬酰胺残基上的 N-乙酰葡萄糖胺上的岩藻糖。Ao38 细胞体积的估计表明,Ao38 细胞比 Sf9 细胞大约大 2.5 倍,但仅约为 High Five 细胞大小的 74%。Ao38 细胞对 AcMNPV 的感染高度敏感,类似于 Sf9 细胞的感染性。从 Ao38 细胞中产生的感染性 AcMNPV 芽生病毒粒子的产量峰值约为 4.5×10^7IU/ml,超过了 High Five 细胞,但低于 Sf9 细胞。Ao38 细胞在静止培养中快速生长,倍增时间为 20.2 小时,并且 Ao38 细胞很容易适应无血清培养基(Sf-900III)和悬浮培养系统。对 Ao38 和 Ascalapha odorata 亲本细胞系的分析表明,这些细胞系没有最近在 High Five 细胞系中被鉴定为偶然因子的α-诺达病毒。
Ao38 细胞代表一种高效的新昆虫细胞系,将可用于异源蛋白表达和生物技术的其他应用。