Josh Tycko

Systematic discovery of protein functions in human cells to understand gene regulation and enable gene therapy



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Josh Tycko

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Department of Neurobiology

Harvard Medical School




Josh Tycko

Systematic discovery of protein functions in human cells to understand gene regulation and enable gene therapy



Department of Neurobiology

Harvard Medical School



Toolbox for Exploring Modular Gene Regulation in Synthetic Biology Training.


Journal article


Michael S. Magaraci, Jessica G Bermudez, Deeksha Yogish, D. H. Pak, Viktor Mollov, Josh Tycko, D. Issadore, Sevile G. Mannickarottu, B. Chow
ACS synthetic biology, 2016

Semantic Scholar DOI PubMed
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Cite

APA   Click to copy
Magaraci, M. S., Bermudez, J. G., Yogish, D., Pak, D. H., Mollov, V., Tycko, J., … Chow, B. (2016). Toolbox for Exploring Modular Gene Regulation in Synthetic Biology Training. ACS Synthetic Biology.


Chicago/Turabian   Click to copy
Magaraci, Michael S., Jessica G Bermudez, Deeksha Yogish, D. H. Pak, Viktor Mollov, Josh Tycko, D. Issadore, Sevile G. Mannickarottu, and B. Chow. “Toolbox for Exploring Modular Gene Regulation in Synthetic Biology Training.” ACS synthetic biology (2016).


MLA   Click to copy
Magaraci, Michael S., et al. “Toolbox for Exploring Modular Gene Regulation in Synthetic Biology Training.” ACS Synthetic Biology, 2016.


BibTeX   Click to copy

@article{michael2016a,
  title = {Toolbox for Exploring Modular Gene Regulation in Synthetic Biology Training.},
  year = {2016},
  journal = {ACS synthetic biology},
  author = {Magaraci, Michael S. and Bermudez, Jessica G and Yogish, Deeksha and Pak, D. H. and Mollov, Viktor and Tycko, Josh and Issadore, D. and Mannickarottu, Sevile G. and Chow, B.}
}

Abstract

We report a toolbox for exploring the modular tuning of genetic circuits, which has been specifically optimized for widespread deployment in STEM environments through a combination of bacterial strain engineering and distributable hardware development. The transfer functions of 16 genetic switches, programmed to express a GFP reporter under the regulation of the (acyl-homoserine lactone) AHL-sensitive luxR transcriptional activator, can be parametrically tuned by adjusting high/low degrees of transcriptional, translational, and post-translational processing. Strains were optimized to facilitate daily large-scale preparation and reliable performance at room temperature in order to eliminate the need for temperature controlled apparatuses, which are both cost-limiting and space-constraining. The custom-designed, automated, and web-enabled fluorescence documentation system allows time-lapse imaging of AHL-induced GFP expression on bacterial plates with real-time remote data access, thereby requiring trainees to only be present for experimental setup. When coupled with mathematical models in agreement with empirical data, this toolbox expands the scalability and scope of reliable synthetic biology experiments for STEM training.


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