| Literature DB >> 29680377 |
Marios Tomazou1, Mauricio Barahona2, Karen M Polizzi3, Guy-Bart Stan4.
Abstract
To perform well in biotechnology applications, synthetic genetic oscillators must be engineered to allow independent modulation of amplitude and period. This need is currently unmet. Here, we demonstrate computationally how two classic genetic oscillators, the dual-feedback oscillator and the repressilator, can be re-designed to provide independent control of amplitude and period and improve tunability-that is, a broad dynamic range of periods and amplitudes accessible through the input "dials." Our approach decouples frequency and amplitude modulation by incorporating an orthogonal "sink module" where the key molecular species are channeled for enzymatic degradation. This sink module maintains fast oscillation cycles while alleviating the translational coupling between the oscillator's transcription factors and output. We characterize the behavior of our re-designed oscillators over a broad range of physiologically reasonable parameters, explain why this facilitates broader function and control, and provide general design principles for building synthetic genetic oscillators that are more precisely controllable.Keywords: biosensors; computational biology; genetic oscillators; mutual information; orthogonal amplitude and period modulation; periodic signal generator in biology; protease; robustness; synthetic biology
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Year: 2018 PMID: 29680377 DOI: 10.1016/j.cels.2018.03.013
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304