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ESE 680-003 Special topics in electrical and systems engineering: Systems Biology Pappas Kumar Rubin Julius Halász Roadmap to Systems Biology What next? • Cellular processes come down to molecular interactions – Rate laws – Kinetic constants – Differential equations • … so all we need to do is get all the reactions ,rate laws, constants, put them into a computer virtual cell What next? • Easier said than done: – Processes not typically known in detail – Kinetic constants • Not measurable/Not measurable in vivo • Meaningless – High dimensional, nonlinear systems • Yet often simple behavior: emergence – Even if individual processes can be studied, the cost of going through all of them is prohibitive What next? • Biologists have “told us so”: – Reductionism doesn’t work – There are exceptions to all “laws” – Qualitative descriptions are more meaningful • Source of limitations – Experimental input – Lack of fundamental understanding of processes – Lack of appropriate mathematical “language” What next? • Systems/quantitative biology today: – No mathematically expressed principles – Several qualitative principles • Robustness • Redundancy – Driven by experimental data – Certain clusters of modeling activity – Physics, circa 1670 (before Newton) • Incremental progress on many fronts • Best approach is to try to be useful to biology Some of the fronts • • • • • • • Genetic network identification Metabolic networks Signaling Cycles (cell, circadian) Mesoscopic / stochastic phenomena Synthetic biology Software tools Genetic network identification • Microarrays – One of the most spectacular advances in experimental technique – Typical of “high-throughput” approach – Made possible by • Genome sequencing projects of the 1990’s • Semiconductor, microchip technology Genetic network identification • Microarrays – Chips with a grid of RNA* microprobes – Each probe has a different sequence* – Probes represent genes – Probes hybridize to mRNA from a sample – Optical (fluorescence) readout • Parallel measurement of gene expression – Commercially available for several organisms • Affymetrix – “the Microsoft of biotechnology” Gene network identification • What can we learn from high throughput, semi-quantitative, perhaps time resolved, gene expression data? • Identification of transcription networks – Ignore all details of interactions – Focus on the existence of an influence of Gene A onto Gene B – Various levels of abstraction, from on/off to Hill coefficients Gene network identification • • • • Next lecture Papers by Collins, Liao A whole industry has been spawned Lots of room for new ideas coming from computer science/hybrid systems • Challenge: connect with biological knowledge Metabolic networks • Another “breadth-first” approach • Made possible by arduous work of many postdocs, PubMed, and other databases • Metabolic reactions curated into comprehensive databases • Stoichiometric information on hundreds of concurrent chemical reactions • The workings of the chemical factory Metabolic networks • The state of the system is the vector of all metabolite concentrations c. • Each reaction is represented by an integer vector: A + B 3X [-1, -1, 3, 0] 2A + B Y [-2, -1, 0, 1] • Stoichiometric matrix S • Vector of reaction rates v • External fluxes of metabolites f c S v f Metabolic networks • At steady state, c is constant • The state of the metabolic network is v • Many possible solutions – Feasiblity cone – Which state is picked by nature? – Determined by unknown kinetic details • Models postulate optimization principles Metabolic networks • Many papers: – Palsson, Church • Lecture by Marcin Imielinski (?) • Lots of linear algebra Signaling • Multi-cellular organisms are similar to highly organized societies – Every cell has the same genetic information – Yet they are highly specialized/differentiated – Widely different phenotypes, functions – The organism works because each cell does what it is supposed to Signaling ensures that cells act properly Signaling • In cancer, the signaling machinery breaks down – Wrong signals and/or wrong interpretation – Cells differentiate into the wrong type – They grow when they are not supposed to – Stop listening to the system commands – Take a life of their own (tumors) Signaling • Signaling tells cells to do everything – Lack of certain signals triggers cell suicide (apoptosis) • Signals are carried by special molecules in the organism – Hormones, growth factors • There are specialized receptors on the cell surface • Receptors transduce signals (binding of their ligand) into the cytosol (the inside of the cell) • Signaling cascades originate in the initial binding event • Complicated networks of multistep phosphorylation reactions • Eventually they control gene expression Signaling • Signaling malfunctions result from small mutations – Lack of signaling – Uninduced signals – Over/under- amplification • A few well studied networks – EGF Erb/Her • A few well studied cell lines Cell signaling • Huge literature • Lecture: Avi Ghosh (Drexel) Mesoscopic phenomena • Face the reality of small molecule numbers • Stochastic nature of reactions • Well established simulation methods • Often ignored, wrongly Mesoscopic phenomena • A few important results – Lambda phage (Arkin) – Lac system (van Oudenaarden) – Competence (Elowitz) • Relevant experimental results – Well delimited, controlled, yet live system • Lecture by Mustafa Khammash Cycles • Complicated control systems • Make sure that actions are taken in the correct sequence • Cell cycle – Papers by Tyson • Circadian cycle – Papers by Doyle Synthetic biology • From simple genetic switches • To tumor killing bacteria • In between: synthesis of artemisin (Keasling) Software • • • • • Large industry Lots of potential for new work Largely ten years behind in modeling Focus on languages standardization,.. Still very important