SmartBac是一种新的杆状病毒系统,用于生产大的蛋白质复合物

IF 3.5 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yujia Zhai , Danyang Zhang , Leiye Yu , Fang Sun , Fei Sun
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引用次数: 17

摘要

近年来低温电子显微镜技术的革新为解决无结晶大分子复合物的高分辨率结构打开了新的大门,而如何高效地获得均匀的大分子复合物样品也因此成为一个瓶颈。在这里,我们报告了SmartBac,一个简单而通用的系统,用于构建大尺寸的转移质粒,用于在昆虫细胞中产生表达大的多蛋白复合物的重组杆状病毒。SmartBac系统集成了单载体质粒融合系统、Gibson组装法和多蛋白策略来构建最终的转移质粒。设计荧光蛋白与靶标共表达以监测转染和表达效率。提供了一种筛选最佳标记亚基以进行有效纯化的方案。成功地表达和纯化了6个大型多蛋白复合物,包括人囊复合物和动力蛋白复合物,这表明SmartBac系统在未来的广泛应用中具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SmartBac, a new baculovirus system for large protein complex production

SmartBac, a new baculovirus system for large protein complex production

Recent revolution of cryo-electron microscopy has opened a new door to solve high-resolution structures of macromolecule complexes without crystallization while how to efficiently obtain homogenous macromolecule complex sample is therefore becoming a bottleneck. Here we report SmartBac, an easy and versatile system for constructing large-sized transfer plasmids used to generate recombinant baculoviruses that express large multiprotein complexes in insect cells. The SmartBac system integrates the univector plasmid-fusion system, Gibson assembly method and polyprotein strategy to construct the final transfer plasmid. The fluorescent proteins are designed co-expressed with the target to monitor transfection and expression efficiencies. A scheme of screening an optimal tagged subunit for efficient purification is provided. Six large multiprotein complexes including the human exocyst complex and dynactin complex were successfully expressed and purified, suggesting a great potential of SmartBac system for its wide application in the future.

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来源期刊
Journal of Structural Biology: X
Journal of Structural Biology: X Biochemistry, Genetics and Molecular Biology-Structural Biology
CiteScore
6.50
自引率
0.00%
发文量
20
审稿时长
62 days
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