Difference between revisions of "Team:William and Mary/Measurement"

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For our project this year we successfully designed and characterized an accessible and modular degradation-based system for the control of gene expression speed. Utilizing an <i>E. coli</i> orthogonal tmRNA degradation system consisting of a  <i>Mesoplasma florum</i> Lon (mf-Lon) protease [1] and highly engineered tmRNA tags [2] with a range of protease affinities, we were able to create a qualitative and quantitative gene expression speed change that was dependent on degradation rate. To do this we first had developed a time course measurement protocol that would allow robust and reproducible single cell measurements. Developing this method was time intensive, and meant that we spent a large portion of the summer without getting high-quality gene expression speed data, but ultimately our final <a href='https://2017.igem.org/Team:William_and_Mary/Protocols' style='text-decoration: underline;'>time course protocol</a> ensured that we got <a href='https://2017.igem.org/Team:William_and_Mary/Results' style='text-decoration: underline;'>robust, reproducible data</a> that we could feel confident in.  
 
For our project this year we successfully designed and characterized an accessible and modular degradation-based system for the control of gene expression speed. Utilizing an <i>E. coli</i> orthogonal tmRNA degradation system consisting of a  <i>Mesoplasma florum</i> Lon (mf-Lon) protease [1] and highly engineered tmRNA tags [2] with a range of protease affinities, we were able to create a qualitative and quantitative gene expression speed change that was dependent on degradation rate. To do this we first had developed a time course measurement protocol that would allow robust and reproducible single cell measurements. Developing this method was time intensive, and meant that we spent a large portion of the summer without getting high-quality gene expression speed data, but ultimately our final <a href='https://2017.igem.org/Team:William_and_Mary/Protocols' style='text-decoration: underline;'>time course protocol</a> ensured that we got <a href='https://2017.igem.org/Team:William_and_Mary/Results' style='text-decoration: underline;'>robust, reproducible data</a> that we could feel confident in.  
 
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<div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;'> Beyond simply tracking gene expression over time to obtain basic speed measurements, we were able to successfully measure and exert control over more complex aspects of the temporal dynamics of gene expression. Informed by our mathematical model, we not only predicted but executed a functional <a href="https://2017.igem.org/Team:William_and_Mary/Dynamic_Control"><u>incoherent feedforward loop</u></a> enabling control over pulse-like behavior using our protein degradation system. To that end, we provided a thorough characterization of gene expression dynamics over time, comparing simultaneous induction to pre-induction of protease to yield qualitatively different results. </div>
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<div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;'>Furthermore, </div>
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Revision as of 23:57, 1 November 2017



Overview
For our project this year we successfully designed and characterized an accessible and modular degradation-based system for the control of gene expression speed. Utilizing an E. coli orthogonal tmRNA degradation system consisting of a Mesoplasma florum Lon (mf-Lon) protease [1] and highly engineered tmRNA tags [2] with a range of protease affinities, we were able to create a qualitative and quantitative gene expression speed change that was dependent on degradation rate. To do this we first had developed a time course measurement protocol that would allow robust and reproducible single cell measurements. Developing this method was time intensive, and meant that we spent a large portion of the summer without getting high-quality gene expression speed data, but ultimately our final time course protocol ensured that we got robust, reproducible data that we could feel confident in.
Beyond simply tracking gene expression over time to obtain basic speed measurements, we were able to successfully measure and exert control over more complex aspects of the temporal dynamics of gene expression. Informed by our mathematical model, we not only predicted but executed a functional incoherent feedforward loop enabling control over pulse-like behavior using our protein degradation system. To that end, we provided a thorough characterization of gene expression dynamics over time, comparing simultaneous induction to pre-induction of protease to yield qualitatively different results.
Furthermore,
We believe that our team should be considered for this award not only for the quality of our characterization but also for our choice of what properties to measure. Rigorous measurements of the temporal aspects of genetic processes are overshadowed by an emphasis on the characterization of concentration- or strength-dependent features. This bias is so strong that even though the mf-Lon protein degradation tags have been available to the community since 2014, no direct experimental demonstrations of the relationship between genetic response speed and degradation rate existed in the synthetic biology literature before our project. By emphasizing the importance of temporal circuit dynamics and providing future iGEM teams with a modular, simple and predictable system to control and measure those dynamical properties by altering gene expression speed, our project helps to drive iGEM forward as a continual innovator in making the kinds of enabling measurements which open the door to qualitatively new technologies.
References
[1] Eyal Gur and Robert T Sauer. Evolution of the ssra degradation tag in mycoplasma: specificity switch to a different protease. Proceedings of the National Academy of Sciences, 105(42):16113– 16118, 2008.
[2] D Ewen Cameron and James J Collins. Tunable protein degradation in bacteria. Nature biotechnology, 32(12):1276–1281, 20