Difference between revisions of "Team:William and Mary/Composite Part"

We utilized a suite of 6 protein degradation tags (pdts) originally designed by [Collins et al 2014]. Each tag confers a distinct level of protein degradation; tags are lettered (A-F) in order of protease affinity, from strongest (highest level of degradation) to weakest. These parts have been made BioBrick compatible, codon-optimized for E. coli, and placed in between UNS sites, so that teams may easily insert them after their gene of choice using Gibson Assembly. They are also flanked by BsaI cut sites, for ease of use with Golden Gate Assembly. This allows future teams to efficiently adapt the speed-control system to their own parts and circuits, regardless of their preferred assembly method.

Our next collection of parts consist of a protein degradation tagged mScarlet reporter under the control of the strong constitutive promoter J23100. These parts, in combination with inducible mf-Lon protease constructs (listed below), allowed us to characterize the degradation properties of each protein degradation tag on a plasmid-based system. We successfully demonstrated distinct levels of protein degradation by each of the 6 pdt’s; see our full characterization here [HYPERLINK TO RESULTS PAGE]. We also included a tagless control construct (J23100 mScarlet with no pdt) as a comparison. In order to demonstrate that our protein degradation tags operated similarly regardless of the tagged protein, we also built and characterized analogous constructs with an sfGFP reporter; these are listed below in the “All Parts” table. mScarlet and sfGFP reporters have been codon-optomized for E. coli and feature a double stop codon.

We further include a collection of 6 aTc-inducible mScarlet-I reporter constructs tagged with each respective protein degradation tag (and a pdt-less inducible mScarlet-I control construct), all under the control of the pTet promoter. This collection of parts was used in our gene expression speed measurements, allowing us to control the initiation of reporter expression using the small molecule aTc. We used these constructs along with the IPTG-inducible mf-Lon protease (listed directly below) to demonstrate distinct levels of speed to steady state in reporter expression proportional to the relative strength of each pdt; the full results of these experiments are found here (HYPERLINK TO RESULTS PAGE). We also took advantage of the inducible nature of these constructs by manipulating levels of aTc exposure in order to adjust final steady state values independently of speed control; the details of our readjustment experiments are found here (HYPERLINK TO RESULTS PAGE). Once again, we also created analogous constructs for each of these parts, replacing mScarlet with sfGFP. These constructs are listed in the All Parts table at the bottom of this page.

Our gene expression speed control system features the E. coli-orthogonal mf-Lon protease originally characterized by [sauer citation] , which specifically targets the above protein degradation tags with varying affinities corresponding to varying degradation rates. We have modified the mf-Lon gene via codon-optimization for iGEM use and added a double terminator (for details see [link basic part]). We have submitted mf-Lon constructs that are inducible by IPTG and arabinose, respectively. We used the IPTG-inducible mf-Lon construct in tandem with the above aTc-inducible pdt reporter constructs to obtain gene expression speed measurements--these results can be found here (HYPERLINK TO RESULTS PAGE).

As part of our collaboration with the University of Maryland iGEM team, we built 6 additional constructs incorporating our protein degradation tags onto their CueR-based copper sensor (link to UMD copper sensor part page??). These parts allowed us to demonstrate persistence of speed-change effects for protein outputs beyond simple reporter proteins, and provide an example of a practical application of our speed-control system to improve biosensor output speed. The details of these experiments can be found here (HYPERLINK TO RESULTS PAGE).