Orosa Beatriz, Viczián András
School of Biological and Biomedical Sciences, University of Durham, Durham, County Durham, UK.
Biological Research Centre, Plant Biology Institute, Szeged, Hungary.
Methods Mol Biol. 2019;2026:69-83. doi: 10.1007/978-1-4939-9612-4_5.
Posttranslational modifications (PTMs) happen after or during protein translation. Small Ubiquitin-like Modifier (SUMO) proteins are covalently attached to certain lysine residues of the target proteins to modify their activity, stability, or localization. This process is called SUMOylation, which is a reversible PTM: SUMO protease enzymes can cleave SUMOs off the target protein backbone. Although many ubiquitinated proteins are targeted for degradation, SUMOylation does not necessary lead to the degradation of the modified protein but lead to the regulation of various physiological responses. SUMOylation of the examined protein cannot simply be monitored by immunoblotting techniques performed on total protein extracts, due to the SUMO-specific signals derived from other modified molecules. Furthermore, the fact that only a limited fraction of the target protein pool is SUMOylated makes the detection of SUMOylated proteins challenging. This protocol shows how SUMOylated phytochrome B (phyB) molecules can be detected using homologous and heterologous experimental systems in planta.
翻译后修饰(PTMs)发生在蛋白质翻译之后或期间。小泛素样修饰物(SUMO)蛋白共价连接到靶蛋白的某些赖氨酸残基上,以改变其活性、稳定性或定位。这个过程称为SUMO化,它是一种可逆的翻译后修饰:SUMO蛋白酶可以将SUMO从靶蛋白主链上切割下来。虽然许多泛素化蛋白会被靶向降解,但SUMO化不一定会导致被修饰蛋白的降解,而是会导致各种生理反应的调节。由于来自其他修饰分子的SUMO特异性信号,仅通过对总蛋白提取物进行免疫印迹技术无法简单地监测所检测蛋白的SUMO化。此外,只有有限比例的靶蛋白池被SUMO化这一事实使得SUMO化蛋白的检测具有挑战性。本方案展示了如何在植物中使用同源和异源实验系统检测SUMO化的光敏色素B(phyB)分子。