Dickinson Daniel J, Schwager Francoise, Pintard Lionel, Gotta Monica, Goldstein Bob
Department of Biology and Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Cell Physiology and Metabolism, University of Geneva Medical Faculty, 1, rue Michel Servet, 1211 Geneva, Switzerland.
Dev Cell. 2017 Aug 21;42(4):416-434.e11. doi: 10.1016/j.devcel.2017.07.024.
Regulated protein-protein interactions are critical for cell signaling, differentiation, and development. For the study of dynamic regulation of protein interactions in vivo, there is a need for techniques that can yield time-resolved information and probe multiple protein binding partners simultaneously, using small amounts of starting material. Here we describe a single-cell protein interaction assay. Single-cell lysates are generated at defined time points and analyzed using single-molecule pull-down, yielding information about dynamic protein complex regulation in vivo. We established the utility of this approach by studying PAR polarity proteins, which mediate polarization of many animal cell types. We uncovered striking regulation of PAR complex composition and stoichiometry during Caenorhabditis elegans zygote polarization, which takes place in less than 20 min. PAR complex dynamics are linked to the cell cycle by Polo-like kinase 1 and govern the movement of PAR proteins to establish polarity. Our results demonstrate an approach to study dynamic biochemical events in vivo.
受调控的蛋白质-蛋白质相互作用对于细胞信号传导、分化和发育至关重要。为了研究体内蛋白质相互作用的动态调控,需要能够产生时间分辨信息并使用少量起始材料同时探测多个蛋白质结合伙伴的技术。在此,我们描述了一种单细胞蛋白质相互作用测定法。在特定时间点生成单细胞裂解物,并使用单分子下拉法进行分析,从而获得体内动态蛋白质复合物调控的信息。我们通过研究PAR极性蛋白确立了这种方法的实用性,PAR极性蛋白介导多种动物细胞类型的极化。我们发现,秀丽隐杆线虫受精卵的极化过程在不到20分钟内发生,期间PAR复合物的组成和化学计量发生了显著调控。PAR复合物的动态变化通过Polo样激酶1与细胞周期相联系,并控制PAR蛋白的移动以建立极性。我们的结果展示了一种研究体内动态生化事件的方法。