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一种利用增强绿色荧光蛋白(EGFP)介导的纯化和线性化来生成杆状病毒杆粒的新方法。

A novel method for generating baculovirus bacmids using EGFP-mediated purification and linearization.

作者信息

Su Wujie, Gu Haoyi, Zhang Xiaoxia, Wang Wenbing, Li Fanchi, Li Bing

机构信息

School of Life Sciences, Suzhou Medical College of Soochow University, Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.

Department of Preventive Medicine and Public Health Laboratory Science, School of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, Jiangsu, China.

出版信息

Biotechnol Lett. 2025 Jul 17;47(4):77. doi: 10.1007/s10529-025-03619-y.

Abstract

Baculovirus bacmids have been widely used in over-expression and gene deletion. Traditionally, baculovirus bacmids are developed by inserting an 8.6 kbp bacterial DNA cassette into baculovirus genomes either through homologous recombination in cultured cells or via in vitro cloning. In this study, by introducing Bsu36i-attached egfp to the 8.6 kbp bacterial DNA cassette, we develop a novel method for generating baculovirus bacmids. An 11.6 kbp bacterial DNA cassette containing the introduced egfp was used to generate an intermediate bacmid. With the EGFP reporter, purification was performed in cultured cells, increasing the proportions of recombinants. The intermediate bacmid containing the 11.6 kbp bacterial DNA cassette was obtained by transforming DH10B competent cells with viral DNA after 3 rounds of purification. The intermediate bacmid DNA was linearized by digestion with Bsu36i and then was co-transfected with the PCR-amplified 8.6 kbp bacterial cassette into BmN cells, where homologous recombination occurred between them. The final BmNPV bacmid was obtained by transforming DH10B competent cells with viral DNA. Capable of increasing the proportions of recombinants via purification and linearization, this method has great potential to be used for bacmid generation for baculoviruses, especially those that are not capable of producing high titers of viruses.

摘要

杆状病毒杆粒已广泛应用于过表达和基因缺失研究。传统上,杆状病毒杆粒是通过在培养细胞中进行同源重组或体外克隆,将一个8.6 kbp的细菌DNA盒插入杆状病毒基因组而构建的。在本研究中,通过将携带egfp的Bsu36i引入8.6 kbp的细菌DNA盒,我们开发了一种生成杆状病毒杆粒的新方法。使用一个包含引入的egfp的11.6 kbp细菌DNA盒来生成中间杆粒。利用EGFP报告基因,在培养细胞中进行纯化,提高了重组体的比例。经过三轮纯化后,用病毒DNA转化DH10B感受态细胞,获得了包含11.6 kbp细菌DNA盒的中间杆粒。用Bsu36i酶切使中间杆粒DNA线性化,然后与PCR扩增的8.6 kbp细菌盒共转染到BmN细胞中,它们之间发生同源重组。用病毒DNA转化DH10B感受态细胞,获得最终的BmNPV杆粒。该方法能够通过纯化和线性化提高重组体的比例,在杆状病毒杆粒的构建中具有很大的应用潜力,尤其是对于那些不能产生高滴度病毒的杆状病毒。

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