arXiv subjects

Nida Obatake

Publications and source records attributed to Nida Obatake.

6 recordsLinked to original sources

arXiv2022

Newton-Okounkov bodies of chemical reaction systems

Despite their noted potential in polynomial-system solving, there are few concrete examples of Newton-Okounkov bodies arising from applications. Accordingly, in this paper, we introduce a new application of Newton-Okounkov body theory to the study of chemical reaction networks, and compute several examples. An important invariant of a chemical reaction network is its maximum number of positive steady states, which is realized as the maximum number of positive real roots of a parametrized polynomial system. Here, we introduce a new upper bound on this number, namely the `Newton-Okounkov body bound' of a chemical reaction network. Through explicit examples, we show that the Newton-Okounkov body bound of a network gives a good upper bound on its maximum number of positive steady states. We also compare this Newton-Okounkov body bound to a related upper bound, namely the mixed volume of a chemical reaction network, and find that it often achieves better bounds.

q-bio.MN↗

arXiv2020

Mixed volume of small reaction networks

An important invariant of a chemical reaction network is its maximum number of positive steady states. This number, however, is in general difficult to compute. Nonetheless, there is an upper bound on this number -- namely, a network's mixed volume -- that is easy to compute. Moreover, recent work has shown that, for certain biological signaling networks, the mixed volume does not greatly exceed the maximum number of positive steady states. Continuing this line of research, we further investigate this overcount and also compute the mixed volumes of small networks, those with only a few species or reactions.

q-bio.MN↗

arXiv2019

Dynamics of ERK regulation in the processive limit

We consider a model of extracellular signal-regulated kinase (ERK) regulation by dual-site phosphorylation and dephosphorylation, which exhibits bistability and oscillations, but loses these properties in the limit in which the mechanisms underlying phosphorylation and dephosphorylation become processive. Our results suggest that anywhere along the way to becoming processive, the model remains bistable and oscillatory. More precisely, in simplified versions of the model, precursors to bistability and oscillations (specifically, multistationarity and Hopf bifurcations, respectively) exist at all "processivity levels". Finally, we investigate whether bistability and oscillations can exist together.

q-bio.MN↗

arXiv2019

Identifiability of Linear Compartmental Models: The Effect of Moving Inputs, Outputs, and Leaks

A mathematical model is identifiable if its parameters can be recovered from data. Here we investigate, for linear compartmental models, whether (local, generic) identifiability is preserved when parts of the model -- specifically, inputs, outputs, leaks, and edges -- are moved, added, or deleted. Our results are as follows. First, for certain catenary, cycle, and mammillary models, moving or deleting the leak preserves identifiability. Next, for cycle models with up to one leak, moving inputs or outputs preserves identifiability. Thus, every cycle model with up to one leak (and at least one input and at least one output) is identifiable. Next, we give conditions under which adding leaks renders a cycle model unidentifiable. Finally, for certain cycle models with no leaks, adding specific edges again preserves identifiability. Our proofs, which are algebraic and combinatorial in nature, rely on results on elementary symmetric polynomials and the theory of input-output equations for linear compartmental models.

math.DS↗

arXiv2019

Oscillations and bistability in a model of ERK regulation

This work concerns the question of how two important dynamical properties, oscillations and bistability, emerge in an important biological signaling network. Specifically, we consider a model for dual-site phosphorylation and dephosphorylation of extracellular signal-regulated kinase (ERK). We prove that oscillations persist even as the model is greatly simplified (reactions are made irreversible and intermediates are removed). Bistability, however, is much less robust -- this property is lost when intermediates are removed or even when all reactions are made irreversible. Moreover, bistability is characterized by the presence of two reversible, catalytic reactions: as other reactions are made irreversible, bistability persists as long as one or both of the specified reactions is preserved. Finally, we investigate the maximum number of steady states, aided by a network's "mixed volume" (a concept from convex geometry). Taken together, our results shed light on the question of how oscillations and bistability emerge from a limiting network of the ERK network -- namely, the fully processive dual-site network -- which is known to be globally stable and therefore lack both oscillations and bistability. Our proofs are enabled by a Hopf bifurcation criterion due to Yang, analyses of Newton polytopes arising from Hurwitz determinants, and recent characterizations of multistationarity for networks having a steady-state parametrization.

q-bio.MN↗

arXiv2018

On the identification of $k$-inductively pierced codes using toric ideals

Neural codes are binary codes in $\{0,1\}^n$; here we focus on the ones which represent the firing patterns of a type of neurons called place cells. There is much interest in determining which neural codes can be realized by a collection of convex sets. However, drawing representations of these convex sets, particularly as the number of neurons in a code increases, can be very difficult. Nevertheless, for a class of codes that are said to be $k$-inductively pierced for $k=0,1,2$ there is an algorithm for drawing Euler diagrams. Here we use the toric ideal of a code to show sufficient conditions for a code to be 1- or 2-inductively pierced, so that we may use the existing algorithm to draw realizations of such codes.

q-bio.NC↗