Department of Physics, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, USA.
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
Cell Biol Int. 2022 May;46(5):683-700. doi: 10.1002/cbin.11762. Epub 2022 Jan 30.
The emergence of labeling strategies and live cell imaging methods enables the imaging of chromatin in living cells at single digit nanometer resolution as well as milliseconds temporal resolution. These technical breakthroughs revolutionize our understanding of chromatin structure, dynamics and functions. Single molecule tracking algorithms are usually preferred to quantify the movement of these intranucleus elements to interpret the spatiotemporal evolution of the chromatin. In this review, we will first summarize the fluorescent labeling strategy of chromatin in live cells which will be followed by a systematic comparison of live cell imaging instrumentation. With the proper microscope, we will discuss the image analysis pipelines to extract the biophysical properties of the chromatin. Finally, we expect to give practical suggestions to broad biologists on how to select methods and link to the model properly according to different investigation purposes.
标记策略和活细胞成像方法的出现使我们能够以单个纳米分辨率和毫秒时间分辨率对活细胞中的染色质进行成像。这些技术突破彻底改变了我们对染色质结构、动态和功能的理解。通常优先使用单分子跟踪算法来量化这些核内元素的运动,以解释染色质的时空演化。在这篇综述中,我们将首先总结活细胞中染色质的荧光标记策略,然后对活细胞成像仪器进行系统比较。有了合适的显微镜,我们将讨论图像分析管道,以提取染色质的生物物理特性。最后,我们希望根据不同的研究目的,为广大生物学家提供如何选择方法并正确链接模型的实用建议。