Dynamic Modeling of Cell-Free Biochemical Networks Using Effective Kinetic Models

Abstract

Cell-free systems offer many advantages for the study, manipulation and modeling of metabolism compared to in vivo processes. Many of the challenges confronting genome-scale kinetic modeling can potentially be overcome in a cell-free system. For example, there is no complex transcriptional regulation to consider, transient metabolic measurements are easier to obtain, and we no longer have to consider cell growth. Thus, cell-free operation holds several significant advantages for model development, identification and validation. Theoretically, genome-scale cell-free kinetic models may be possible for industrially important organisms, such as E. coli, if a simple, tractable framework for integrating allosteric regulation with enzyme kinetics can be formulated. Toward this unmet need, we present an effective biochemical network modeling framework for building dynamic cell-free metabolic models. The key innovation of our approach is the integration of simple effective rules encoding complex allosteric regulation with traditional kinetic pathway modeling. We tested our approach by modeling the time evolution of several hypothetical cell-free metabolic networks. We found that simple effective rules, when integrated with traditional enzyme kinetic expressions, captured complex allosteric patterns such as ultra sensitivity or non-competitive inhibition in the absence of mechanistic information. Second, when integrated into network models, these rules captured classic regulatory patterns such as product-induced feedback inhibition. Lastly, we showed, at least for the network architectures considered here, that we could simultaneously estimate kinetic parameters and allosteric connectivity from synthetic data starting from an unbiased collection of possible allosteric structures using particle swarm optimization.

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Document Details

Document Type
Technical Report
Publication Date
Mar 03, 2015
Accession Number
AD1027865

Entities

People

  • Adithya Sagar
  • Jeffrey D Varner
  • Joseph A. Wayman

Organizations

  • University of California, Santa Barbara

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Algorithms
  • Biology
  • Cell-Free System
  • Cells
  • Computational Biology
  • Computational Science
  • Engineering
  • Enzyme Kinetics
  • Equations
  • Experimental Data
  • Kinetics
  • Metabolism
  • Particle Swarm Optimization
  • Steady State
  • Synthetic Biology
  • Systems Biology
  • Transfer Functions

Fields of Study

  • Biology
  • Computer science

Readers

  • Computational Modeling and Simulation
  • Molecular Genetics
  • Molecular and Cellular Biochemistry