Department of Biotechnology and Biosciences, University of Milano-Bicocca, 20125 Milan, Italy.
STAR Protoc. 2022 Feb 3;3(1):101146. doi: 10.1016/j.xpro.2022.101146. eCollection 2022 Mar 18.
Here we describe a protocol for the generation of site-specific DNA damage, including double and single strand breaks, using the 405 nm laser of a confocal microscope in cells pre-sensitized with Hoechst. This is a simple approach, particularly useful to assess the involvement of proteins and the roles of liquid-liquid phase separation in DNA damage repair. Examples of transfection protocol, drug concentrations, and microscopy are provided, although optimization may be needed for specific experimental setups and cell lines used. For complete details on the use and execution of this protocol, please refer to Levone et al. (2021).
在这里,我们描述了一种在经 Hoechst 预敏化的细胞中使用共聚焦显微镜的 405nm 激光产生特定位置的 DNA 损伤的方案,包括双链和单链断裂。这是一种简单的方法,特别有助于评估蛋白质的参与以及液-液相分离在 DNA 损伤修复中的作用。提供了转染方案、药物浓度和显微镜的示例,尽管可能需要针对特定的实验设置和使用的细胞系进行优化。如需详细了解本方案的使用和执行情况,请参阅 Levone 等人(2021 年)。