= Meeting Abstracts and Slides =
=== Prof Arun Lahiri Majumdar and Dr Sonali Sengupta (Bose Institute) ===
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 '''Plant Systems' Biology: A Bird's Eye View'''


  . [[attachment:Majumdar.ppt|Download the slides]]

=== Dr Ashwani Pareek (Jawaharlal Nehru University, New Delhi) (with Neeta Lakra, Khalid Anwar and Sneh L Singla-Pareek) ===
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 '''Dissecting out the complex trait of abiotic stress tolerance in plants: will a systems biology approach be of some help?'''

  . Abiotic   stresses cause a significant decline in crop yield worldwide. We are   trying to dissect of the complex trait of salinity and drought response   in rice plants. Contemporary tools of transcriptomics, proteomics,   Ionomics, metabolomics etc are being used to understand the response of   rice seedlings towards these stresses. One of the important conclusion   which can be drawn easily from these analysis is that the response is   quite complex in nature. Hundereds of genes, proteins and metabolites   are found to be up regulated or down regulated in rice seedlings within   few minutes of salinity stress. The question still remains with us -   which gene shall we engineer? which genes should be pyramided? will   systems biology approach provide a solution to this? We have picked up a   set of "candidate genes" from this list and have used the tools of   functional genomics to validate the role of these unknown genes in   stress tolerance. Data pertaining to these experiments will be   discussed.

  . Slides not available

=== Dr Mark Poolman (Oxford Brookes University) ===
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 '''Genome-Scale Metabolic Modelling and its Application to Rice'''

  . This talk will introduce some of the common concepts of and theoretical basis of the analysis of metabolic models. These will be illustrated by their application to a recently constructed geneome scale model of Rice, specifically, how may we expect reaction fluxes to be redistributed given vriable light intensity nd a constant demand for biomass  components.

  . The results of this analysis suggest that different areas of metbolism, associated with energy production may show distinct and seperate, but nonetheless coordinated, responses at different levels of light intensity.

  . [[attachment:Poolman.pdf|Download the slides]]

=== Dr Sudip Kundu (University of Calcutta) ===
 . '''Analysis Of Metabolic Interactions Between Cellular Compartments In Rice'''

  . I shall present the potential function units of metabolism ofdifferent cellular compartments of rice. An analysis based on the in-silico deletion of the enzymatic genes would also be discussed. I shall also present how the  constraints imposed on intracellular transporters can vary the metabolic response of genome scale metabolism. Finally, integration of some transcriptomic data to analyze the metabolic efficiency would also be presented.

  . [[attachment:Kundu.ppt|Download the slides]]

=== Dr Hemant Ritturaj Kushwaha (ICGEB, New Delhi) ===
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 '''Pathway analysis in view of whole genome studies'''


  . Abstract/ slides not available

=== Dr Christine Faulkner (Oxford Brookes University) ===
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 '''The regulation of cell-to-cell communication during pathogen invasion'''

  . Cell-to-cell communication is a fundamental biological process, necessary for co-ordination of development and environmental responses in multicellular organisms. The receptor-like protein AtLYM2 is located at plasmodesmata and mediates chitin-triggered changes to cell-to-cell communication during fungal pathogen invasion . AtLYM2 functions independently of the chitin receptor CERK1 and thus identifies that there are multiple chitin perception mechanisms in plants.

  . [[attachment:Faulkner.pptx|Download the slides]]

=== Dr Nick Kruger (University of Oxford) ===
 . '''Probing the performance of central carbon metabolism in plant cells by ^13^C-metabolic flux analysis'''

  . Flux provides the most informative measure of the functioning of a metabolic network. In this talk I wish to consider recent developments in the implementation of steady-state stable-isotope (^13^C) metabolic flux analysis (MFA) to define the flux phenotype of plant systems. I will illustrate the contribution of MFA in dissecting network performance of carbon metabolism in a heterotrophic cell culture of Arabidopsis to changes in mineral nutrient status.

=== Prof A S Raghavendra (University of Hyderabad) ===
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 '''Optimisation of Photosynthesis by Multiple Intracellular Compartments in Plant Cells: A Systems Biochemistry Outlook'''

  . Key  metabolic processes in plant cells depend on dynamic inter-organelle  interactions.  The crosstalk between compartments is mediated by  multiple signals, such as, metabolite movements, redox status and even  pH.  My talk would describe the signalling network between chloroplasts,  mitochondria, peroxisomes, and cytoplasm, which achieves not only  optimisation of photosynthesis but also protects against  photoinhibition.

  . [[attachment:Raghavendra.ppt|Download the slides]]


=== Prof David Fell (Oxford Brookes University) ===
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 '''Modelling Tomato Fruit Metabolism'''

  .
  Both  genetic and environmental factors have a strong and multifaceted  influence on tomato fruit quality. They act and interact in such a  complex way that it is extremely difficult to study their effects by  experiment alone.  The EraSysBio project ''Fruit Integrative Modelling''  involves partners from Oxford and two groups in France. We aim to build  a virtual tomato fruit that enables the prediction of metabolite levels  given genetic and environmental inputs, by an iterative process between  laboratories that combine expertise in fruit biology, ecophysiology,  theoretical and experimental biochemistry, and biotechnology. Our  component is to build a kinetic model encompassing the routes carbon  takes, once imported into the fruit cells from the source organs of the  mother plant.  This will be combined with To integrate the kinetic model  with a phenomenological model predicting sugar and organic acid  contents as functions of time, light intensity, temperature and water  availability being developed in one of the French labs.  Our approach to  building the metabolic simulation will be described, as well as its  context within the whole project.

  . [[attachment:Fell.pdf|Download the slides]].  See also the [[http://frim.brookes.ac.uk/video|video]] shown in the talk.

=== Dr Anu Raghunathan (National Chemical Laboratory, Pune) ===
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 '''From cell lines to Tissue specific Flux Balance Models:  Cancer Cell Growth and Metabolism'''

  . Complex multi-hit, multi phenotype diseases like cancer have poor prognosis and their etiology is difficult to fathom due to multi-factorial emergent responses of the human system. Patients of such diseases would benefit highly from a personalized and individualized approach for treatment. Constraints-based flux balance models seem to provide such a platform for data integration and analysis of complex diseases. The focus of this talk is the development and analysis of tissue specific models for cancer. Global microarray gene expression data is used to develop cell-line and patient models for lung cancer using from legacy data using the genome scale model of human metabolism, Recon1 as the basis. The paradigm for metabolic systems biology as applied to lung cancer will be discussed in the context of computing the cancer phenotype. The predictions of clinical models using tissue data and blood data will be compared to the classical cell line models. Integration of results of routine blood work, specialized clinical tests like PET (Positron Emission Tomography) scans allow for better prognosis but also fundamental understanding of the disease. The challenge of such a task in the context of flux balance metabolic models for predictive differentiation of progressive disease states and their ability to predict outcomes will also be discussed.

  . Slides not available

=== Prof K V Venkatesh (Dept Chemical Engineering, IIT Bombay) (with Pramod Somvanshi and Anil Patel) ===
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 '''Multi-scale Structured Kinetic Model for Analyzing Disease States in Metabolic Syndrome'''

  . Metabolic syndrome is among the most complex diseases with multiple complications associated with it such as insulin   resistance,   central   obesity,   Type   2   diabetes,   hypercholesterolemia, hypertension, atherosclerosis and coronary artery disease. It has been found that these are system level diseases with defects at metabolic, signaling and genetic levels rather than defects in individual biological entities. In metabolic syndrome, insulin resistance is the key defects which affect various metabolic processes. Defects in insulin secretion, its activity, and its signaling generate insulin resistance. Insulin signaling pathway orchestrates its response with various other pathways coupled with feedback mechanisms to generate multiple effects. Moreover various other hormones and inflammatory pathways are known to modulate the insulin activity. Insulin resistance is thus a combinatorial effect of all these factors.

  . The systems biological approach with mathematical modeling of the biological networks serves as an important way to assess these diseases. We attempt to integrate the models of meal simulation, whole body metabolism, insulin signaling pathway and insulin secretion which scale from cellular to organ levels. We assort to the kinetic modeling and analysis of the integrated network and analyze the metabolic response with respect to perturbation in various parameters of the model. The detailed integrated network of various affected metabolic, signaling and genetic pathways is prepared. The kinetic models are developed that describe various interactions. Parameter values and other constants are collected from the literature and are also estimated through optimization and curve fitting for the model. The models are then simulated for sensitivity and phase-plane analysis to notice the key parameters that have major influence on the overall network behavior. Furthermore, Perturbation analysis is performed to get the matrix of parameters for healthy and disease phenotype. Such an analysis helps in understanding the system dynamics and help in answering various ‘What-if’ kinds of questions that can aid in identification of potential drug targets and design effective therapies. We further extend the analysis to address the link between metabolism and tumor genesis by extending the above model by integrating P53 pathway to AKT-PTEN and further representing the regulation of metabolism through HIF1 activity. Analysis shows that the perturbation at AKT node can affect metabolism leading to tumor genesis demonstrating Warburg Effect. Thus the model for the whole-body metabolism including signaling pathways can yield insights into the emergence of disease states.

  . [[attachment:Venkatesh.ppt|Download the slides]]

=== Dr Santanu Datta (Cellworks) ===
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 '''Delineating the genetic and chemical vulnerability of anti-infective drug targets'''

  . The  equity of a drug target is majorly evaluated by its genetic  vulnerability with tools ranging from antisense and microRNA driven  knockdowns to induced expression of the target protein. In order to  upgrade the process of antibacterial target identification and discern  its most effective type of inhibition, an in silico tool box that  evaluates its genetic and chemical vulnerability leading either to  stasis or cidal outcome was constructed and validated.

  . [[attachment:Datta.ppt|Download the slides]]