Inferring local molecular dynamics from the global actin network structure: A case study of 2D synthetic branching actin networks

被引:0
作者
Rostami, Minghao W. [1 ]
Bannish, Brittany E. [2 ]
Gasior, Kelsey [3 ]
Pinals, Rebecca L. [4 ]
Copos, Calina [5 ,6 ]
Dawes, Adriana T. [7 ,8 ]
机构
[1] Binghamton Univ, Dept Math & Stat, Binghamton, NY USA
[2] Univ Cent Oklahoma, Dept Math & Stat, Edmond, OK USA
[3] Univ Notre Dame, Dept Appl & Computat Math & Stat, Notre Dame, IN USA
[4] MIT, Picower Inst Learning & Memory, Boston, MA USA
[5] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[6] Northeastern Univ, Dept Math, Boston, MA 02115 USA
[7] Ohio State Univ, Dept Math, Columbus, OH 43210 USA
[8] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
基金
美国国家科学基金会; 美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
Actin; Branched actin network; Lamellipodium; Machine learning; Agent-based model; Cell cytoskeleton; ARP2/3; COMPLEX; MOTILITY; ORGANIZATION; FILAMENTS;
D O I
10.1016/j.jtbi.2023.111613
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cells rely on their cytoskeleton for key processes including division and directed motility. Actin filaments are a primary constituent of the cytoskeleton. Although actin filaments can create a variety of network architectures linked to distinct cell functions, the microscale molecular interactions that give rise to these macroscale structures are not well understood. In this work, we investigate the microscale mechanisms that produce different branched actin network structures using an iterative classification approach. First, we employ a simple yet comprehensive agent-based model that produces synthetic actin networks with precise control over the microscale dynamics. Then we apply machine learning techniques to classify actin networks based on measurable network density and geometry, identifying key mechanistic processes that lead to particular branched actin network architectures. Extensive computational experiments reveal that the most accurate method uses a combination of supervised learning based on network density and unsupervised learning based on network symmetry. This framework can potentially serve as a powerful tool to discover the molecular interactions that produce the wide variety of actin network configurations associated with normal development as well as pathological conditions such as cancer.
引用
收藏
页数:15
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