论文标题
在Covid-19时期建模:基于统计和规则的中尺度模型
Modeling in the Time of COVID-19: Statistical and Rule-based Mesoscale Models
论文作者
论文摘要
我们提出了一种新技术,用于快速建模和构建科学准确的中尺度生物学模型。最终的3D模型基于几个2D显微镜扫描,以及有关代表的一组几何关系的生物实体的最新知识。我们的新技术基于统计和基于规则的建模方法,这些方法是迅速作者,快速构建且易于修改的方法。从几个2D显微镜扫描中,我们了解各种结构方面的统计特性,例如外膜形状,空间特性和大分子在膜上的分布特性。此信息用于3D模型构建中。一旦将所有成像证据纳入模型,就可以通过在空间表征其余生物实体的规则(例如大分子之间的相互作用,它们对其他结构的距离和方向)进行交互定义规则来纳入其他信息。这些规则是通过直观的3D交互式可视化和建模反馈循环来定义的。我们在SARS-COV-2病毒颗粒超微结构的建模过程中证明了方法的实用性。我们在这里提出的第一个完整的原子模型可以将生物学研究引导到战斗病毒传播方面的新方向。
We present a new technique for rapid modeling and construction of scientifically accurate mesoscale biological models. Resulting 3D models are based on few 2D microscopy scans and the latest knowledge about the biological entity represented as a set of geometric relationships. Our new technique is based on statistical and rule-based modeling approaches that are rapid to author, fast to construct, and easy to revise. From a few 2D microscopy scans, we learn statistical properties of various structural aspects, such as the outer membrane shape, spatial properties and distribution characteristics of the macromolecular elements on the membrane. This information is utilized in 3D model construction. Once all imaging evidence is incorporated in the model, additional information can be incorporated by interactively defining rules that spatially characterize the rest of the biological entity, such as mutual interactions among macromolecules, their distances and orientations to other structures. These rules are defined through an intuitive 3D interactive visualization and modeling feedback loop. We demonstrate the utility of our approach on a use case of the modeling procedure of the SARS-CoV-2 virus particle ultrastructure. Its first complete atomistic model, which we present here, can steer biological research to new promising directions in fighting spread of the virus.