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= <font style="color:brown">Research</font> =
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The group research activities are in the area of systems biology with particular emphasis in the development and application of systems theoretic tools for modeling, analysis, and control of diseases, including cancer and other infectious illnesses. The overarching goal is to elucidate the causality in diseases through modeling and systems analysis for the identification of drug targets, disease biomarkers, and other treatments. <BR> The specific applications include:
==Aging==
# Reverse-engineering of stochastic biological systems
# Synergistic analysis of apoptotic inducing cancer drugs,
# Modeling of quorum sensing bacterial infection.
We are working closely with cancer biologists and infectious disease experts to validate and implement the results of our research.


<font style="color:maroon"> <b> Reverse-engineering of Stochastic Biological Systems </b> </font>
;<font style="color:brown"> <b> Stochastic Modeling of Mitochondrial Mutagenesis </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:LakshmiNarayanan_Lakshmanan|LakshmiNarayanan Lakshmanan]]<br>
: <p align='justify'> Mitochondria are intracellular membrane bound organelles, which are believed to be originated through prokaryotic endosymbiosis. Mitochondria posses their own circular DNA and also they perform a myriad of functions inside a living cell (e.g.) ATP production, TCA cycle, Fatty Acid oxidation, Calcium signaling and Apoptosis. Dysfunction of mitochondria due to mitochondrial DNA mutations has been consistently observed with aging and degenerative diseases.  In our lab we are interested in quantitative analysis of formation and accumulation of mitochondrial DNA mutations using stochastic models in different model organisms.  Mutagenesis is an inherently stochastic process with different mutation load and spectrum in different cells of same tissue, hence stochastic formulation of chemical kinetics is used along with the knowledge about different aspects of mitochondrial DNA mutations to model the mutation process. [[Gunawan:LakshmiNarayanan_Lakshmanan| more...]]</p>


A cell can be likened to a microscopic chemical plant, where different cellular components (mRNAs, proteins) are produced, transformed, and consumed (or degraded) to accomplish myriad cellular functions. However, unlike a typical chemical plant, cellular processes, such as gene transcription and protein translation, involve very low concentrations of molecules (on the order of nanomolar). Such low concentration means that these processes can only occur intermittently as discrete and random events. The intrinsic stochastic behavior gives rise to variations in cellular phenotype, even in clonal cell population. Thus, to understand the functioning behavior of a biological network, the intrinsic variations in cellular processes should be explicitly taken into consideration in the system modeling. Here, we are developing a reverse-engineering framework for the identification of biological models that can represent the discrete stochastic nature of processes in a cell. This framework will explicitly consider the stochastic variations in cellular processes and the robust characteristics of cellular systems in the reverse engineering steps
;<font style="color:brown"> <b> Reverse-engineering of Stochastic Biological Systems </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:Suresh_Poovathingal|Suresh Kumar Poovathingal]]<br>
: <b>Collaborators :</b> Jan Gruber & [http://www.med.nus.edu.sg/bioweb/acad_staff/barry_halliwell.html Barry Halliwell]
: <p align='justify'> A cell can be seen as a microscopic chemical plant, where different cellular components (mRNAs, proteins) are produced, transformed, and consumed (or degraded) to accomplish myriad cellular functions. However, unlike a typical chemical plant, cellular processes, such as gene transcription and protein translation, involve very low concentrations of molecules (on the order of nanomolar). Such low concentration means that these processes can only occur intermittently as discrete and random events. The intrinsic stochastic behavior gives rise to variations in cellular phenotype, even in clonal cell population. Thus, to understand the functioning behavior of a biological network, the intrinsic variations in cellular processes should be explicitly taken into consideration in the system modeling. Here, we are developing a reverse-engineering framework for the identification of biological models that can represent the discrete stochastic nature of processes in a cell. This framework will explicitly consider the stochastic variations in cellular processes and the robust characteristics of cellular systems in the reverse engineering steps. In our preliminary investigation we have implemented a point mutation stochastic framework in unraveling the inherent stochastic nature of aging process. The stochastic model is based on the mitochondrial free radical theory of aging, which implicates the mutations in mitochondrial genome to be largely responsible for the organism’s aging. [[Gunawan:Suresh_Poovathingal| more...]]</p>


   
;<font style="color:brown"> <b> Mitochondria dynamics and the propagation of mtDNA mutant </b> </font> <br>
: <b>Investigator :</b> [[Gunawan:Tam_Zhi_Yang|Tam Zhi Yang]]<br>
: <p align='justify'> mtDNA mutation has been implicated as a contributing factor that causes aging. Mitochondria is commonly referred to as the powerhouse of a cell. Far from being a static organelle in the cell, mitochondria continuously moves around the cytoplasm (directed movement) and can undergo fusion and fission with other mitochondria. It could also undergo mitochondrial biogenesis to multiply in numbers and can be removed via mitophagy. How does these dynamics contribute to the maintenance of mtDNA mutation is not known, and the focus of my study is to understand this through modeling of the mitochondria dynamics in silico</p>


<font style="color:maroon"> <b> Synergistic Analysis of Apoptosis Network </b> </font>
==Tools==


Apoptosis is the machinery of programmed cell death (cell suicide), whose failure has been associated with many diseases including cancer. Indeed, reinstating apoptosis in has become a major strategy in new cancer drug development, some of which currently under clinical trials. Though promising, many of these drugs have limited effectiveness when used individually. Nevertheless, scientists have found that cocktails of drugs can have synergistic activities beyond the cumulative efficacy of each drug. The identification of such cocktails however is still done in an ad-hoc manner. The goal of this research is to develop system analysis tools that can assist the identification of synergistic drugs combination, and can further suggest scheduling and (relative) dosing of these drugs, through mathematical modeling. Conversely, the same analysis tool can also be used to identify synergistic toxicity of different cancer drugs when used at the same time. Using models of cancerous and healthy cells, such analysis can also characterize drug(s) that will induce apoptosis with a specific efficacy in tumor cells.
;<font style="color:brown"> <b> Parameter Estimation of Oscillatory Systems </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:Ang Kok Siong|Ang, Kok Siong]]<br>
: <p align='justify'>Oscillatory behavior is exhibited by many biological systems. Examples these include the circadian rhythm and p53-mdm2 response to DNA damage. Such dynamical behavior is important and integral of a higher biological function, such as sleeping and feeding patterns (circadian rhythm) and DNA repair (p53-mdm2). To study these systems, in-silico models have been developed to aid in the analysis. However, the corresponding model parameters are usually chosen qualitatively such that the system to exhibit the general characteristics of experimental data. The focus of the research here is to facilitate reconciliation of the model with experimental data in a quantitative manner. [[Gunawan:Ang Kok Siong| more...]]</p>




<font style="color:maroon"> <b> Quorum Sensing of P. aeruginosa Bacterial Infection </b> </font>
;<font style="color:brown"> <b> Metabolic Model Identification Parameter Estimation and Structure Identification  </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:Jia Gengjie|Jia Gengjie]]<br>
: <p align='justify'>The inverse modeling of dynamic metabolic pathways is challenging, a model identification cycle is proposed based on the work of many scientists. To make this cycle complete, a streamlined work-flow is needed, consisting of solving the potential problems encountered in the process. These problems include data issues, computational issues, and mathematical issues associated with parameter estimation algorithms and structure identification strategies.This project focuses on parameter estimation and structure identification, tackling those challenges. Specifically, there are three proposals which have been tested or are going to be tested. [[Gunawan:Jia Gengjie| more...]]</p>  


In the natural environment, cells do not live independently, but rather they interact with each other. In a bacterial colony, for example, the survival of a single bacterium should become secondary to that of the whole population. One of such interactions is the cell-to-cell signalling, known as quorum sensing, which is used to sense population density and to synchronize gene expression. Some of these bacteria have been associated with infections in human and animals, such as P. aeruginosa which causes infections in immunocompromised patients. The goals of the research are to establish an accurate dynamical representation of QS population using a population balance model, to understand the implications of QS on the sensitivity and robustness properties of a single cell and the colony through the application of system analysis, and finally to identify the treatment options and procedures for infection caused by QS bacteria through model-based optimization. The specific application of the research is on P. aeruginosa virulence. The framework for representing cell population dynamics in this work will have general applicability to other multicellular biological systems.
 
 
;<font style="color:brown"> <b> Model Identification in Biochemical Systems Theory </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:Sridharan Srinath|Sridharan Srinath]]<br>
: <p align='justify'> Recent advances in technology permit high throughput experiments at genomic, transcriptomic, proteomic and metabolomic levels. The information obtained from time-series data, however, is implicit and requires extensive data analysis.The focus of this work is to investigate the identifiability of metabolic network models (particularly BST models), and to suggest model refinement or experimental design that maximizes the number of estimable parameters from data. Two types of identifiability property are considered. First, a priori identifiability analysis yields the identifiable parameters under the assumption of noise-free data. Parametric sensitivities are used as a basis for selecting the a priori identifiable parameters. Secondly, practical identifiability gives the identifiable parameters when the data are contaminated with noise. In other words, this analysis gives the accuracy with which the parameters can be estimated. The practical identifiability analysis methods are based on linear(ized) and nonlinear regression analysis, particularly the statistical inference of confidence interval or region of the parameter estimates. [[Gunawan:Sridharan Srinath| more...]]</p>
 
 
 
;<font style="color:brown"> <b> Robustness Analysis in Systems Biology </b> </font> <br>
: <b>Investigator  :</b> [[Gunawan:Thanneer Malai|Thanneer Malai Perumal]]<br>
: <p align='justify'> Biological Robustness, an evolved property of biological systems gives rise to cellular functioning and complexity. Hence understanding robustness will enhance our understanding of cellular pathways and underlying mechanisms. The focus of our research is in developing novel robustness measures and analysis methodologies for both deterministic and stochastic models of cellular signalling networks. Of particular interest is the development of an effective sensitivity based methodology named Two-Time Molecular Sensitivity (TTMS) analysis complementing the existing Parametric Sensitivity analysis. We have also successfully developed a novel local TTMS analysis for deterministic models and applied to various cellular signalling pathways. In practice, the analysis can guide model identification and reduction of cellular systems and suggest experimentally testable hypotheses. In addition, the biological knowledge gained can assist drug discovery efforts in the identification of potential drug targets, the understanding of drug efficacy and specificity, and finally the optimization of drug dosing and timing. [[Gunawan:Thanneer Malai| more...]]</p>

Latest revision as of 03:14, 12 February 2011

Chemical and Biological Systems Engineering Laboratory

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Aging

Stochastic Modeling of Mitochondrial Mutagenesis
Investigator  : LakshmiNarayanan Lakshmanan

Mitochondria are intracellular membrane bound organelles, which are believed to be originated through prokaryotic endosymbiosis. Mitochondria posses their own circular DNA and also they perform a myriad of functions inside a living cell (e.g.) ATP production, TCA cycle, Fatty Acid oxidation, Calcium signaling and Apoptosis. Dysfunction of mitochondria due to mitochondrial DNA mutations has been consistently observed with aging and degenerative diseases. In our lab we are interested in quantitative analysis of formation and accumulation of mitochondrial DNA mutations using stochastic models in different model organisms. Mutagenesis is an inherently stochastic process with different mutation load and spectrum in different cells of same tissue, hence stochastic formulation of chemical kinetics is used along with the knowledge about different aspects of mitochondrial DNA mutations to model the mutation process. more...

Reverse-engineering of Stochastic Biological Systems
Investigator  : Suresh Kumar Poovathingal
Collaborators : Jan Gruber & Barry Halliwell

A cell can be seen as a microscopic chemical plant, where different cellular components (mRNAs, proteins) are produced, transformed, and consumed (or degraded) to accomplish myriad cellular functions. However, unlike a typical chemical plant, cellular processes, such as gene transcription and protein translation, involve very low concentrations of molecules (on the order of nanomolar). Such low concentration means that these processes can only occur intermittently as discrete and random events. The intrinsic stochastic behavior gives rise to variations in cellular phenotype, even in clonal cell population. Thus, to understand the functioning behavior of a biological network, the intrinsic variations in cellular processes should be explicitly taken into consideration in the system modeling. Here, we are developing a reverse-engineering framework for the identification of biological models that can represent the discrete stochastic nature of processes in a cell. This framework will explicitly consider the stochastic variations in cellular processes and the robust characteristics of cellular systems in the reverse engineering steps. In our preliminary investigation we have implemented a point mutation stochastic framework in unraveling the inherent stochastic nature of aging process. The stochastic model is based on the mitochondrial free radical theory of aging, which implicates the mutations in mitochondrial genome to be largely responsible for the organism’s aging. more...

Mitochondria dynamics and the propagation of mtDNA mutant
Investigator  : Tam Zhi Yang

mtDNA mutation has been implicated as a contributing factor that causes aging. Mitochondria is commonly referred to as the powerhouse of a cell. Far from being a static organelle in the cell, mitochondria continuously moves around the cytoplasm (directed movement) and can undergo fusion and fission with other mitochondria. It could also undergo mitochondrial biogenesis to multiply in numbers and can be removed via mitophagy. How does these dynamics contribute to the maintenance of mtDNA mutation is not known, and the focus of my study is to understand this through modeling of the mitochondria dynamics in silico

Tools

Parameter Estimation of Oscillatory Systems
Investigator  : Ang, Kok Siong

Oscillatory behavior is exhibited by many biological systems. Examples these include the circadian rhythm and p53-mdm2 response to DNA damage. Such dynamical behavior is important and integral of a higher biological function, such as sleeping and feeding patterns (circadian rhythm) and DNA repair (p53-mdm2). To study these systems, in-silico models have been developed to aid in the analysis. However, the corresponding model parameters are usually chosen qualitatively such that the system to exhibit the general characteristics of experimental data. The focus of the research here is to facilitate reconciliation of the model with experimental data in a quantitative manner. more...


Metabolic Model Identification Parameter Estimation and Structure Identification
Investigator  : Jia Gengjie

The inverse modeling of dynamic metabolic pathways is challenging, a model identification cycle is proposed based on the work of many scientists. To make this cycle complete, a streamlined work-flow is needed, consisting of solving the potential problems encountered in the process. These problems include data issues, computational issues, and mathematical issues associated with parameter estimation algorithms and structure identification strategies.This project focuses on parameter estimation and structure identification, tackling those challenges. Specifically, there are three proposals which have been tested or are going to be tested. more...


Model Identification in Biochemical Systems Theory
Investigator  : Sridharan Srinath

Recent advances in technology permit high throughput experiments at genomic, transcriptomic, proteomic and metabolomic levels. The information obtained from time-series data, however, is implicit and requires extensive data analysis.The focus of this work is to investigate the identifiability of metabolic network models (particularly BST models), and to suggest model refinement or experimental design that maximizes the number of estimable parameters from data. Two types of identifiability property are considered. First, a priori identifiability analysis yields the identifiable parameters under the assumption of noise-free data. Parametric sensitivities are used as a basis for selecting the a priori identifiable parameters. Secondly, practical identifiability gives the identifiable parameters when the data are contaminated with noise. In other words, this analysis gives the accuracy with which the parameters can be estimated. The practical identifiability analysis methods are based on linear(ized) and nonlinear regression analysis, particularly the statistical inference of confidence interval or region of the parameter estimates. more...


Robustness Analysis in Systems Biology
Investigator  : Thanneer Malai Perumal

Biological Robustness, an evolved property of biological systems gives rise to cellular functioning and complexity. Hence understanding robustness will enhance our understanding of cellular pathways and underlying mechanisms. The focus of our research is in developing novel robustness measures and analysis methodologies for both deterministic and stochastic models of cellular signalling networks. Of particular interest is the development of an effective sensitivity based methodology named Two-Time Molecular Sensitivity (TTMS) analysis complementing the existing Parametric Sensitivity analysis. We have also successfully developed a novel local TTMS analysis for deterministic models and applied to various cellular signalling pathways. In practice, the analysis can guide model identification and reduction of cellular systems and suggest experimentally testable hypotheses. In addition, the biological knowledge gained can assist drug discovery efforts in the identification of potential drug targets, the understanding of drug efficacy and specificity, and finally the optimization of drug dosing and timing. more...