串联亲和纯化
烟草蚀刻病毒
蛋白酶
融合蛋白
蛋白质纯化
蛋白质A/G
蛋白质G
标志标签
蛋白质A
钙调蛋白
蛋白质-蛋白质相互作用
亲和层析
靶蛋白
结合蛋白
化学
生物化学
劈理(地质)
生物
抗体
病毒
重组DNA
遗传学
植物病毒
酶
基因
马铃薯Y病毒
断裂(地质)
古生物学
作者
Julie Viala,Emmanuelle Bouveret
出处
期刊:Methods in molecular biology
日期:2023-11-07
卷期号:: 285-297
被引量:4
标识
DOI:10.1007/978-1-0716-3445-5_19
摘要
The discovery of protein-protein interaction networks can lead to the unveiling of protein complex(es) forming cellular machinerie(s) or reveal component proteins of a specific cellular pathway. Deciphering protein-protein interaction networks therefore contributes to a deeper understanding of how cells function. Here we describe the protocol to perform tandem affinity purification (TAP) in bacteria, which enables the identification of the partners of a bait protein under native conditions. This method consists in two sequential steps of affinity purification using two different tags. For that purpose, the bait protein is translationally fused to the TAP tag, which consists of a calmodulin-binding peptide (CBP) and two immunoglobulin G (IgG)-binding domains of Staphylococcus aureus protein A (ProtA) that are separated by the tobacco etch virus (TEV) protease cleavage site. After the first round of purification based on the binding of ProtA to IgG-coated beads, TEV protease cleavage releases CBP-tagged bait protein along with its partners for a second round of purification on calmodulin affinity resin and leaves behind protein contaminants bound to IgG. Creating the TAP-tag translational fusion at the chromosomal locus allows detection of protein interactions occurring in physiological conditions.
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