生物素化
链霉亲和素
泛素
NEDD8公司
体内
转基因
生物
分子生物学
生物化学
化学
癌症研究
细胞生物学
生物素
泛素连接酶
遗传学
基因
作者
Marina Serrano‐Maciá,Teresa C. Delgado,María Luz Martínez‐Chantar
出处
期刊:Methods in molecular biology
日期:2022-11-29
卷期号:: 151-162
被引量:3
标识
DOI:10.1007/978-1-0716-2859-1_11
摘要
In the last years, our group and others have uncovered the role of ubiquitin (Ub) and ubiquitin-like proteins such as the neural precursor cell expressed, developmentally downregulated 8 (NEDD8)-mediated modifications in several types of liver disease, including nonalcoholic fatty liver disease, liver fibrosis, and hepatocellular carcinoma. For this purpose, we have taken advantage of biotinylated ubiquitin (bioUb) and biotinylated NEDD8 (bioNEDD8) mice, transgenic mouse models in which ubiquitin and NEDD8, respectively, are biotinylated in vivo. Using these genetic tools and pull-down assays that exploit the strong biotin-streptavidin interaction, denaturing lysis conditions, and stringent washing procedures, only proteins modified by Ub or NEDD8 are isolated from mammalian tissues in vivo. Here, we report a protocol of streptavidin pull-down of ubiquitinated and NEDDylated liver proteins using the bioUb and bioNEDD8 mice that can potentially be used to characterize both the hepatic ubiquitome and NEDDylome in different models of liver injury.
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