J. Vesco, F. Harris, S. Dascalu, Del R. Jackson, J. Baker
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引用次数: 2
Abstract
Some of the work done in the Baker lab at the University of Nevada, Reno has been directed towards the analysis of muscle tissue in a single molecule arrangement. The process is a novel high-throughput single molecule binding assay or SiMBA for short. This assay is performed by binding single-headed skeletal muscle myosin to a cover slip and looking at how the fluorescently labeled actin filaments bind to these myosin as imaged with a fluorescence microscope. The conditions are varied and the effects on actin-myosin binding kinetics are observed. In order to analyze the binding times and unbound times, a researcher must observe the interactions and manually collect the data. This particular method of data collection is tedious and time consuming, thereby making this portion of the experiment the "rate limiting" factor for producing results in a timely manner. As this can take many hours to analyze a one minute long movie, an automated or semi-automated solution would be beneficial to this assay. This paper presents the design and implementation of a semi-automated solution for identifying and tracking a variable number of objects that exhibit a multitude of behaviors, and extracting the specific behaviors of motion and stagnation as well as the duration of these behaviors.
内华达大学里诺分校(University of Nevada, Reno)的贝克实验室(Baker lab)所做的一些工作是针对单分子排列的肌肉组织进行分析的。该方法是一种新型的高通量单分子结合试验,简称SiMBA。该试验通过将单头骨骼肌肌球蛋白结合到覆盖片上,并观察荧光标记的肌动蛋白丝如何与这些肌球蛋白结合,并用荧光显微镜成像。观察了不同条件对肌动蛋白-肌球蛋白结合动力学的影响。为了分析绑定时间和未绑定时间,研究人员必须观察相互作用并手动收集数据。这种特殊的数据收集方法是冗长而耗时的,因此使这部分实验成为及时产生结果的“速率限制”因素。由于分析一分钟长的电影可能需要几个小时,因此自动化或半自动化的解决方案将有利于此分析。本文提出了一种半自动化解决方案的设计和实现,用于识别和跟踪表现出多种行为的可变数量的对象,并提取运动和停滞的特定行为以及这些行为的持续时间。