Broucke Ellen, Rolland Filip, Crepin Nathalie
Plant Metabolic Signaling Lab, Biology Department, KU Leuven, Heverlee, Leuven, Belgium.
KU Leuven Plant Institute (LPI), KU Leuven, Heverlee, Leuven, Belgium.
Methods Mol Biol. 2023;2642:215-231. doi: 10.1007/978-1-0716-3044-0_12.
Phosphorylation/dephosphorylation is a key posttranslational mechanism for signal transduction and amplification. Several techniques exist for assessing protein phosphorylation status, but each has its own drawbacks. The fast, straightforward, and low-tech approach described here uses transient overexpression of peptide-tagged proteins in Arabidopsis leaf mesophyll protoplasts and immunoblotting with Phos-tag™ SDS-PAGE and commercial anti-tag antibodies. We illustrate this with two relevant examples related to the SnRK1 protein kinase, which mediates metabolic stress signaling: Arabidopsis thaliana SnRK1 activation by T-loop (auto-)phosphorylation and SnRK1 phosphorylation of the Arabidopsis RAV1 transcription factor, which is involved in seed germination and early seedling development.
磷酸化/去磷酸化是信号转导和放大的关键翻译后机制。目前有多种技术可用于评估蛋白质的磷酸化状态,但每种技术都有其自身的缺点。本文所描述的快速、直接且技术要求较低的方法,是利用拟南芥叶片叶肉原生质体中肽标签蛋白的瞬时过表达,并结合使用Phos-tag™ SDS-PAGE和商业化抗标签抗体进行免疫印迹分析。我们通过与SnRK1蛋白激酶相关的两个实例对此进行说明,SnRK1蛋白激酶介导代谢应激信号传导:拟南芥SnRK1通过T环(自)磷酸化激活,以及参与种子萌发和幼苗早期发育的拟南芥RAV1转录因子的SnRK1磷酸化。