The Francis Crick Institute, London, NW1 1AT, UK.
Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.
Sci Rep. 2024 Aug 28;14(1):20032. doi: 10.1038/s41598-024-70925-2.
Recent advances in light microscopy have enabled single molecules to be imaged and tracked within living cells and this approach is impacting our understanding of cell biology. Computer modeling and simulation are important adjuncts to the experimental cycle since they aid interpretation of experimental results and help refine, test and generate hypotheses. Object-oriented computer modeling is particularly well-suited for simulating random, thermal, movements of individual molecules as they interact with other molecules and subcellular structures, but current models are often limited to idealized systems consisting of unit volumes or planar surfaces. Here, a simulation tool is described that combines a 3-dimensional, voxelated, representation of the cell consisting of subcellular structures (e.g. nucleus, endoplasmic reticulum, cytoskeleton, vesicles, and filopodia) combined with numerical floating-point precision simulation of thousands of individual molecules moving and interacting within the 3-dimensional space. Simulations produce realistic time-series video sequences comprising single fluorophore intensities and realistic background noise which can be directly compared to experimental fluorescence video microscopy data sets.
近年来,光学显微镜技术的进步使得我们能够在活细胞内对单个分子进行成像和跟踪,这种方法正在影响我们对细胞生物学的理解。计算机建模和模拟是实验周期的重要辅助手段,因为它们有助于解释实验结果,并帮助改进、测试和生成假说。面向对象的计算机建模特别适合于模拟单个分子与其他分子和亚细胞结构相互作用时的随机、热运动,但当前的模型通常仅限于由单位体积或平面组成的理想化系统。这里描述了一种模拟工具,它将由亚细胞结构(如核、内质网、细胞骨架、囊泡和丝状伪足)组成的细胞的三维体素化表示与对数千个在三维空间中移动和相互作用的单个分子的数值浮点精度模拟相结合。模拟生成的真实时间序列视频序列包含单个荧光团强度和真实背景噪声,可以直接与实验荧光视频显微镜数据集进行比较。