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dc.contributor.authorMiller, Miles Aaron
dc.contributor.authorHafner, Marc
dc.contributor.authorSontag, Eduardo
dc.contributor.authorDavidsohn, Noah Justin
dc.contributor.authorSubramanian, Sairam
dc.contributor.authorPurnick, Priscilla E. M.
dc.contributor.authorLauffenburger, Douglas A.
dc.contributor.authorWeiss, Ron
dc.date.accessioned2013-02-21T19:39:41Z
dc.date.available2013-02-21T19:39:41Z
dc.date.issued2012-07
dc.date.submitted2012-04
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/77187
dc.description.abstractSynthetic biology efforts have largely focused on small engineered gene networks, yet understanding how to integrate multiple synthetic modules and interface them with endogenous pathways remains a challenge. Here we present the design, system integration, and analysis of several large scale synthetic gene circuits for artificial tissue homeostasis. Diabetes therapy represents a possible application for engineered homeostasis, where genetically programmed stem cells maintain a steady population of β-cells despite continuous turnover. We develop a new iterative process that incorporates modular design principles with hierarchical performance optimization targeted for environments with uncertainty and incomplete information. We employ theoretical analysis and computational simulations of multicellular reaction/diffusion models to design and understand system behavior, and find that certain features often associated with robustness (e.g., multicellular synchronization and noise attenuation) are actually detrimental for tissue homeostasis. We overcome these problems by engineering a new class of genetic modules for ‘synthetic cellular heterogeneity’ that function to generate beneficial population diversity. We design two such modules (an asynchronous genetic oscillator and a signaling throttle mechanism), demonstrate their capacity for enhancing robust control, and provide guidance for experimental implementation with various computational techniques. We found that designing modules for synthetic heterogeneity can be complex, and in general requires a framework for non-linear and multifactorial analysis. Consequently, we adapt a ‘phenotypic sensitivity analysis’ method to determine how functional module behaviors combine to achieve optimal system performance. We ultimately combine this analysis with Bayesian network inference to extract critical, causal relationships between a module's biochemical rate-constants, its high level functional behavior in isolation, and its impact on overall system performance once integrated.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH NIGMS grant R01GM086881)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Award #1001092)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Graduate Research Fellowship Program)en_US
dc.description.sponsorshipSwiss National Science Foundation (SystemsX.ch grant)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pcbi.1002579en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePublic Library of Scienceen_US
dc.titleModular Design of Artificial Tissue Homeostasis: Robust Control through Synthetic Cellular Heterogeneityen_US
dc.typeArticleen_US
dc.identifier.citationMiller, Miles et al. “Modular Design of Artificial Tissue Homeostasis: Robust Control Through Synthetic Cellular Heterogeneity.” Ed. Greg Tucker-Kellogg. PLoS Computational Biology 8.7 (2012): e1002579. CrossRef. Web.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorMiller, Miles Aaron
dc.contributor.mitauthorHafner, Marc
dc.contributor.mitauthorDavidsohn, Noah Justin
dc.contributor.mitauthorLauffenburger, Douglas A.
dc.contributor.mitauthorWeiss, Ron
dc.relation.journalPLoS Oneen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMiller, Miles; Hafner, Marc; Sontag, Eduardo; Davidsohn, Noah; Subramanian, Sairam; Purnick, Priscilla E. M.; Lauffenburger, Douglas; Weiss, Ronen
dc.identifier.orcidhttps://orcid.org/0000-0003-0396-2443
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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