TY - JOUR
T1 - Rules, hypergraphs, and probabilities: The three-level analysis of chemical reaction systems and other stochastic stoichiometric population processes
AU - Smith, Eric
AU - Smith, Harrison B.
AU - Andersen, Jakob Lykke
PY - 2024/12/5
Y1 - 2024/12/5
N2 - We consider problems in the functional analysis and evolution of combinatorial chemical
reaction networks as rule-based, or three-level systems. The first level consists of rules,
realized here as graph-grammar representations of reaction mechanisms. The second level
consists of stoichiometric networks of molecules and reactions, modeled as hypergraphs.
At the third level is the stochastic population process on molecule counts, solved for dynamics of population trajectories or probability distributions. Earlier levels in the hierarchy generate later levels combinatorially, and as a result constraints imposed in earlier and smaller
layers can propagate to impose order in the architecture or dynamics in later and larger
layers. We develop general methods to study rule algebras, emphasizing system consequences of symmetry; decomposition methods of flows on hypergraphs including the stoichiometric counterpart to Kirchhoff’s current decomposition and work/dissipation relations
studied by Wachtel et al.; and the large-deviation theory for currents in a stoichiometric stochastic population process, deriving additive decompositions of the large-deviation function
that relate a certain Kirchhoff flow decomposition to the extended Pythagorean theorem
from information geometry. The latter result allows us to assign a natural probabilistic cost
to topological changes in a reaction network of the kind produced by selection for catalystsubstrate specificity. We develop as an example a model of biological sugar-phosphate
chemistry from a rule system published by Andersen et al. It is one of the most potentially
combinatorial reaction systems used by biochemistry, yet one in which two ancient, widespread and nearly unique pathways have evolved in the Calvin-Benson cycle and the Pentose Phosphate pathway, which are additionally nearly reverses of one another. We
propose a probabilistic accounting in which physiological costs can be traded off against the
fitness advantages that select them, and which suggests criteria under which these pathways may be optimal.
AB - We consider problems in the functional analysis and evolution of combinatorial chemical
reaction networks as rule-based, or three-level systems. The first level consists of rules,
realized here as graph-grammar representations of reaction mechanisms. The second level
consists of stoichiometric networks of molecules and reactions, modeled as hypergraphs.
At the third level is the stochastic population process on molecule counts, solved for dynamics of population trajectories or probability distributions. Earlier levels in the hierarchy generate later levels combinatorially, and as a result constraints imposed in earlier and smaller
layers can propagate to impose order in the architecture or dynamics in later and larger
layers. We develop general methods to study rule algebras, emphasizing system consequences of symmetry; decomposition methods of flows on hypergraphs including the stoichiometric counterpart to Kirchhoff’s current decomposition and work/dissipation relations
studied by Wachtel et al.; and the large-deviation theory for currents in a stoichiometric stochastic population process, deriving additive decompositions of the large-deviation function
that relate a certain Kirchhoff flow decomposition to the extended Pythagorean theorem
from information geometry. The latter result allows us to assign a natural probabilistic cost
to topological changes in a reaction network of the kind produced by selection for catalystsubstrate specificity. We develop as an example a model of biological sugar-phosphate
chemistry from a rule system published by Andersen et al. It is one of the most potentially
combinatorial reaction systems used by biochemistry, yet one in which two ancient, widespread and nearly unique pathways have evolved in the Calvin-Benson cycle and the Pentose Phosphate pathway, which are additionally nearly reverses of one another. We
propose a probabilistic accounting in which physiological costs can be traded off against the
fitness advantages that select them, and which suggests criteria under which these pathways may be optimal.
U2 - 10.1371/journal.pcsy.0000022
DO - 10.1371/journal.pcsy.0000022
M3 - Journal article
SN - 2837-8830
VL - 1
JO - PLOS Complex Systems
JF - PLOS Complex Systems
IS - 4
M1 - e0000022
ER -