Moon Hyuk-Jin, Kim Hyun-Jung, Lee Dong-Hyun, Mun Seo-Yeong, Woo Soo-Dong
Department of Agricultural Biology, College of Agriculture, Life & Environment Science, Chungbuk National University, Cheongju 28644, Republic of Korea.
IPBL Inc., Cheongju 28644, Republic of Korea.
Insects. 2025 Apr 17;16(4):426. doi: 10.3390/insects16040426.
A baculovirus expression system (BES) for the production of recombinant proteins requires rapid and easy virus titer determination. In this study, a novel direct titration method was developed using a novel Sf9-QE cell line to easily and economically determine virus titers in a short time. This direct titration method can determine virus titers by directly counting the initially infected cells. This method requires the rapid identification of the initial virus-infected cells. The genome of Sf9-QE cells, which fluoresce upon virus infection, was found to contain at least seven copy numbers of the enhanced green fluorescent protein (EGFP) transgene. This result suggests that Sf9-QE cells in the early stages of virus infection can be identified by the high expression of EGFP. It was also shown that for accurate virus titration using the direct titration method, Sf9-QE cells should be used within 3 d of subculturing. Additionally, counting fluorescent cells to establish virus infection should be performed within 15 to 30 h after virus infection for reliable virus titration. The direct titration method using Sf9-QE cells provides a rapid, reliable, and cost-effective alternative for determining baculovirus titers in BES research.
用于生产重组蛋白的杆状病毒表达系统(BES)需要快速且简便地测定病毒滴度。在本研究中,开发了一种新型的直接滴定法,该方法使用新型的Sf9-QE细胞系,能够在短时间内轻松且经济地测定病毒滴度。这种直接滴定法可通过直接计数最初感染的细胞来测定病毒滴度。此方法需要快速识别最初被病毒感染的细胞。发现病毒感染时会发出荧光的Sf9-QE细胞的基因组包含至少七个拷贝数的增强型绿色荧光蛋白(EGFP)转基因。这一结果表明,病毒感染早期的Sf9-QE细胞可通过EGFP的高表达来识别。还表明,为了使用直接滴定法进行准确的病毒滴定,Sf9-QE细胞应在传代培养后3天内使用。此外,为了获得可靠的病毒滴定结果,应在病毒感染后15至30小时内对荧光细胞进行计数以确定病毒感染情况。使用Sf9-QE细胞的直接滴定法为BES研究中杆状病毒滴度的测定提供了一种快速、可靠且经济高效的替代方法。