Raab Christopher A, Wegner Seraphine V
Institute of Physiological Chemistry and Pathobiochemistry, University of Münster, Münster, Germany.
Bio Protoc. 2024 May 20;14(10):e4995. doi: 10.21769/BioProtoc.4995.
The cell-cell adhesion molecule E-cadherin has been intensively studied due to its prevalence in tissue function and its spatiotemporal regulation during epithelial-to-mesenchymal cell transition. Nonetheless, regulating and studying the dynamics of it has proven challenging. We developed a photoswitchable version of E-cadherin, named opto-E-cadherin, which can be toggled OFF with blue light illumination and back ON in the dark. Herein, we describe easy-to-use methods to test and characterise opto-E- cadherin cell clones for downstream experiments. Key features • This protocol describes how to implement optogenetic cell-cell adhesion molecules effectively (described here on the basis of opto-E-cadherin), while highlighting possible pitfalls. • Utilises equipment commonly found in most laboratories with high ease of use. • Phenotype screening is easy and done within a few hours (comparison of cell clusters in the dark vs. blue light in an aggregation assay). • Three different functionality assay systems are described. • After the cell line is established, all experiments can be performed within three days.
细胞间粘附分子E-钙粘蛋白因其在组织功能中的普遍性及其在上皮-间充质细胞转化过程中的时空调节而受到深入研究。尽管如此,调节和研究其动力学已被证明具有挑战性。我们开发了一种可光开关的E-钙粘蛋白版本,称为光控E-钙粘蛋白,它可以通过蓝光照射关闭并在黑暗中重新开启。在此,我们描述了用于测试和表征光控E-钙粘蛋白细胞克隆以进行下游实验的易用方法。主要特点 • 本方案描述了如何有效地实施光遗传学细胞间粘附分子(在此以光控E-钙粘蛋白为例进行描述),同时突出可能的陷阱。 • 使用大多数实验室常见的设备,易于操作。 • 表型筛选简单,在几小时内即可完成(在聚集试验中比较黑暗与蓝光下的细胞簇)。 • 描述了三种不同的功能测定系统。 • 细胞系建立后,所有实验可在三天内完成。