Arakawa Masashi, Morita Eiji
Department of Biochemistry and Molecular Biology, Faculty of Agriculture and Life Science, Hirosaki University, 3 Bunkyo-cho, Hirosaki-shi, Aomori, Japan.
Bio Protoc. 2023 Mar 20;13(6):e4640. doi: 10.21769/BioProtoc.4640.
Co-immunoprecipitation or pull-down assays are frequently used to analyze protein-protein interactions. In these experiments, western blotting is commonly used to detect prey proteins. However, sensitivity and quantification problems remain in this detection system. Recently, the HiBiT-tag-dependent NanoLuc luciferase system was developed as a highly sensitive detection system for small amounts of proteins. In this report, we introduce the method of using HiBiT technology for the detection of prey protein in a pull-down assay. Using this protocol, we demonstrate the formation of a ternary complex consisting of Japanese encephalitis virus NS4B and two host factors, namely valosin-containing protein, and nuclear protein localization protein 4, which is a critical biological event during flavivirus replication in cells.
免疫共沉淀或下拉分析常用于分析蛋白质-蛋白质相互作用。在这些实验中,蛋白质印迹法通常用于检测靶蛋白。然而,该检测系统仍存在灵敏度和定量问题。最近,基于HiBiT标签的纳米荧光素酶系统被开发为一种用于检测少量蛋白质的高灵敏度检测系统。在本报告中,我们介绍了在下拉分析中使用HiBiT技术检测靶蛋白的方法。使用该方案,我们证明了由日本脑炎病毒NS4B与两种宿主因子(即含缬酪肽蛋白和核蛋白定位蛋白4)组成的三元复合物的形成,这是黄病毒在细胞中复制过程中的一个关键生物学事件。