Bao Y, Mugume Y, Bassham D C
Iowa State University, Ames, IA, United States.
Iowa State University, Ames, IA, United States.
Methods Enzymol. 2017;588:497-513. doi: 10.1016/bs.mie.2016.09.090. Epub 2016 Nov 16.
The study of autophagy in plants is rapidly increasing, due to its pivotal and fundamental roles in responding to stressful stimuli, recycling nutrients during senescence, and maintaining growth under normal conditions. Assays for detecting autophagy in plants have generally been based on microscopic observations, providing qualitative information on autophagy activity. Here, we discuss biochemical assays for detecting autophagy, which have the potential for providing more quantitative information, with a focus on immunoblotting with antibodies against ATG8, NBR1, or epitope tags fused to ATG proteins.
由于自噬在植物应对胁迫刺激、衰老过程中循环利用营养物质以及在正常条件下维持生长方面发挥着关键和基础的作用,植物自噬的研究正在迅速增加。检测植物自噬的方法通常基于显微镜观察,可提供有关自噬活性的定性信息。在此,我们讨论用于检测自噬的生化方法,这些方法有可能提供更多定量信息,重点是使用针对ATG8、NBR1或与ATG蛋白融合的表位标签的抗体进行免疫印迹分析。