TY - JOUR
T1 - Reconfiguring Gene Regulatory Neural Network Computing for Regulating Biofilm Formation
AU - Ratwatte, Adrian
AU - Somathilaka, Samitha
AU - Balasubramaniam, Sasitharan
AU - Taggart, Megan
AU - Nair, Keerthi M.
AU - O'riordan, Alan
AU - Dooley, James
N1 - Publisher Copyright:
© 2013 IEEE.
PY - 2025
Y1 - 2025
N2 - The Gene Regulatory Network (GRN) in biological cells orchestrates essential functions for adaptation and survival in diverse environments, drawing on structural similarities with the Artificial Neural Network (ANN), which can be transformed into a Gene Regulatory Neural Network (GRNN). This transformation enables exploration of their natural computing capabilities regarding network reconfigurability and controllability, facilitating dynamic adjustments of gene-gene interaction weights to regulate biological processes. In this paper, we present a control-theoretic model for the GRNN that determines optimal chemical input concentrations, steering the GRNN towards desired weight configurations using the Linear Quadratic Regulator (LQR) approach. This method enhances network robustness by balancing stability and reconfigurability, ensuring responsive weight adjustments in dynamic environments. We develop mathematical models to identify critical genes using a Continuous-Time Markov Chain (CTMC) and derive temporal weight configurations, providing insights into the system's reconfiguration dynamics, while also quantifying stability and reconfigurability. Our findings demonstrate the effectiveness of the control model in mitigating Clostridioides difficile biofilm formation, outperforming sub-optimal and stochastic perturbation inputs, and highlighting the importance of determining optimal inputs for robust network behavior across diverse complexities.
AB - The Gene Regulatory Network (GRN) in biological cells orchestrates essential functions for adaptation and survival in diverse environments, drawing on structural similarities with the Artificial Neural Network (ANN), which can be transformed into a Gene Regulatory Neural Network (GRNN). This transformation enables exploration of their natural computing capabilities regarding network reconfigurability and controllability, facilitating dynamic adjustments of gene-gene interaction weights to regulate biological processes. In this paper, we present a control-theoretic model for the GRNN that determines optimal chemical input concentrations, steering the GRNN towards desired weight configurations using the Linear Quadratic Regulator (LQR) approach. This method enhances network robustness by balancing stability and reconfigurability, ensuring responsive weight adjustments in dynamic environments. We develop mathematical models to identify critical genes using a Continuous-Time Markov Chain (CTMC) and derive temporal weight configurations, providing insights into the system's reconfiguration dynamics, while also quantifying stability and reconfigurability. Our findings demonstrate the effectiveness of the control model in mitigating Clostridioides difficile biofilm formation, outperforming sub-optimal and stochastic perturbation inputs, and highlighting the importance of determining optimal inputs for robust network behavior across diverse complexities.
KW - biofilm formation
KW - Gene regulatory neural network (GRNN)
KW - network reconfigurability
KW - optimal input concentration
KW - stability
UR - https://www.scopus.com/pages/publications/105002034752
U2 - 10.1109/TNSE.2025.3555962
DO - 10.1109/TNSE.2025.3555962
M3 - Article
AN - SCOPUS:105002034752
SN - 2327-4697
VL - 12
SP - 3002
EP - 3014
JO - IEEE Transactions on Network Science and Engineering
JF - IEEE Transactions on Network Science and Engineering
IS - 4
ER -