# Item

ITEM ACTIONSEXPORT

Released

Thesis

#### Constraint-based Analysis of Substructures of Metabolic Networks

##### Locator

There are no locators available

##### Fulltext (public)

Sayed-Amir_Marashi_Diss.pdf

(Any fulltext), 2MB

##### Supplementary Material (public)

There is no public supplementary material available

##### Citation

Marashi, S.-A. (in preparation). Constraint-based Analysis of Substructures of Metabolic Networks.

Cite as: http://hdl.handle.net/11858/00-001M-0000-0010-77AB-9

##### Abstract

Constraint-based methods (CBMs) are promising tools for the analysis of
metabolic networks, as they do not require detailed knowledge of the biochemical
reactions. Some of these methods only need information about the stoichiometric
coefficients of the reactions and their reversibility types, i.e., constraints for
steady-state conditions. Nevertheless, CBMs have their own limitations. For
example, these methods may be sensitive to missing information in the models.
Additionally, they may be slow for the analysis of genome-scale metabolic models.
As a result, some studies prefer to consider substructures of networks, instead of
complete models. Some other studies have focused on better implementations of
the CBMs.
In Chapter 2, the sensitivity of flux coupling analysis (FCA) to missing reactions
is studied. Genome-scale metabolic reconstructions are comprehensive,
yet incomplete, models of real-world metabolic networks. While FCA has proved
an appropriate method for analyzing metabolic relationships and for detecting
functionally related reactions in such models, little is known about the impact of
missing reactions on the accuracy of FCA. Note that having missing reactions is
equivalent to deleting reactions, or to deleting columns from the stoichiometric
matrix. Based on an alternative characterization of flux coupling relations using
elementary flux modes, we study the changes that flux coupling relations may
undergo due to missing reactions. In particular, we show that two uncoupled
reactions in a metabolic network may be detected as directionally, partially or
fully coupled in an incomplete version of the same network. Even a single missing
reaction can cause significant changes in flux coupling relations. In case of two
consecutive E. coli genome-scale networks, many fully-coupled reaction pairs in
the incomplete network become directionally coupled or even uncoupled in the
more complete reconstruction. In this context, we found gene expression correlation
values being significantly higher for the pairs that remained fully coupled
than for the uncoupled or directionally coupled pairs. Our study clearly suggests
that FCA results are indeed sensitive to missing reactions. Since the currently
available genome-scale metabolic models are incomplete, we advise to use FCA
results with care.
In Chapter 3, a different, but related problem is considered. Due to the
large size of genome-scale metabolic networks, some studies suggest to analyze
subsystems, instead of original genome-scale models. Note that analysis of a subsystem
is equivalent to deletion of some rows from the stoichiometric matrix, or
identically, assuming some internal metabolites to be external. We show mathematically
that analysis of a subsystem instead of the original model can lead the
flux coupling relations to undergo certain changes. In particular, a pair of (fully,
partially or directionally) coupled reactions may be detected as uncoupled in the
chosen subsystem. Interestingly, this behavior is the opposite of the flux coupling
changes that may happen due to the existence of missing reactions, or equivalently,
deletion of reactions. We also show that analysis of organelle subsystems has relatively little influence on the results of FCA, and therefore, many of these
subsystems may be studied independent of the rest of the network.
In Chapter 4, we introduce a rapid FCA method, which is appropriate for
genome-scale networks. Previously, several approaches for FCA have been proposed
in the literature, namely flux coupling finder algorithm, FCA based on
minimal metabolic behaviors, and FCA based on elementary flux patterns. To
the best of our knowledge none of these methods are available as a freely available
software. Here, we introduce a new FCA algorithm FFCA (Feasibility-based Flux
Coupling Analysis). This method is based on checking the feasibility of a system
of linear inequalities. We show on a set of benchmarks that for genome-scale
networks FFCA is faster than other existing FCA methods. Using FFCA, flux
coupling analysis of genome-scale networks of S. cerevisiae and E. coli can be
performed in a few hours on a normal PC. A corresponding software tool is freely
available for non-commercial use.
In Chapter 5, we introduce a new concept which can be useful in the analysis
of fluxes in network substructures. Analysis of elementary modes (EMs) is proven
to be a powerful CBM in the study of metabolic networks. However, enumeration
of EMs is a hard computational task. Additionally, due to their large numbers,
one cannot simply use them as an input for subsequent analyses. One possibility
is to restrict the analysis to a subset of interesting reactions, rather than the whole
network. However, analysis of an isolated subnetwork can result in finding incorrect
EMs, i.e. the ones which are not part of any steady-state flux distribution in
the original network. The ideal set of vectors to describe the usage of reactions in
a subnetwork would be the set of all EMs projected onto the subset of interesting
reactions. Recently, the concept of “elementary flux patterns” (EFPs) has been
proposed. Each EFP is a subset of the support (i.e. non-zero elements) of at least
one EM. In the present work, we introduce the concept of ProCEMs (Projected
Cone Elementary Modes). The ProCEM set can be computed by projecting the
flux cone onto the lower-dimensional subspace and enumerating the extreme rays
of the projected cone. In contrast to EFPs, ProCEMs are not merely a set of
reactions, but from the mathematical point of view they are projected EMs. We
additionally prove that the set of EFPs is included in the set of ProCEM supports.
Finally, ProCEMs and EFPs are compared in the study of substructures
in biological networks.