2013/02/19 by Carlos F. Lopez, Jeremy L. Muhlich, John A. Bachman +1 · 3 citations
Biochemistry, Genetics and Molecular Biology · #Gene Regulatory Network Analysis #Protein Structure and Dynamics #Microbial Metabolic Engineering and Bioproduction
paper · doi:10.1038/msb.2013.1
openalex publication_date 2013/02/19 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/02
Mathematical equations are fundamental to modeling biological networks, but as networks get large and revisions frequent, it becomes difficult to manage equations directly or to combine previously developed models. Multiple simultaneous efforts to create graphical standards, rule-based languages, and integrated software workbenches aim to simplify biological modeling but none fully meets the need for transparent, extensible, and reusable models. In this paper we describe PySB, an approach in which models are not only created using programs, they are programs. PySB draws on programmatic modeling concepts from little b and ProMot, the rule-based languages BioNetGen and Kappa and the growing library of Python numerical tools. Central to PySB is a library of macros encoding familiar biochemical actions such as binding, catalysis, and polymerization, making it possible to use a high-level, action-oriented vocabulary to construct detailed models. As Python programs, PySB models leverage tools and practices from the open-source software community, substantially advancing our ability to distribute and manage the work of testing biochemical hypotheses. We illustrate these ideas using new and previously published models of apoptosis.