Ristic Marko, Brockly Frédérique, Piechaczyk Marc, Bossis Guillaume
Equipe Labellisée par la Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, CNRS UMR 5535, Université de Montpellier, CNRS, 1919 Route de Mende, Montpellier, Cedex 5, 34293, France.
Methods Mol Biol. 2016;1449:279-90. doi: 10.1007/978-1-4939-3756-1_17.
The detection of protein-protein interactions by imaging techniques often requires the overexpression of the proteins of interest tagged with fluorescent molecules, which can affect their biological properties and, subsequently, flaw experiment interpretations. The recent development of the proximity ligation assays (PLA) technology allows easy visualization of endogenous protein-protein interactions at the single molecule level. PLA relies on the use of combinations of antibodies coupled to complementary oligonucleotides that are amplified and revealed with a fluorescent probe, each spot representing a single protein-protein interaction. Another application of this technique is the detection of proteins posttranslational modifications to monitor their localization and dynamics in situ. Here, we describe the use of PLA to detect protein SUMOylation, a posttranslational modification related to ubiquitination, as well as interaction of SUMOylated substrates with other proteins, using both adherent and suspension cells.
通过成像技术检测蛋白质-蛋白质相互作用通常需要对标记有荧光分子的目标蛋白质进行过表达,这可能会影响其生物学特性,进而导致实验解释出现偏差。邻近连接分析(PLA)技术的最新发展使得在单分子水平上轻松可视化内源性蛋白质-蛋白质相互作用成为可能。PLA依赖于使用与互补寡核苷酸偶联的抗体组合,这些抗体通过荧光探针进行扩增和显示,每个斑点代表一次单一的蛋白质-蛋白质相互作用。该技术的另一个应用是检测蛋白质的翻译后修饰,以原位监测其定位和动态变化。在这里,我们描述了使用PLA检测蛋白质SUMO化(一种与泛素化相关的翻译后修饰)以及SUMO化底物与其他蛋白质的相互作用,同时使用贴壁细胞和悬浮细胞。