"I've always believed that if you put in the work, the results will come." - Michael Jordan

Results

Figure 1: Transcriptional activity of PcstA during growth measured by RNA levels.

In the following chapter you will all our results from the lab.

Figure 2: Streaks of BTH101 on LB/X-gal plates, containing pSB1C3-T18 + pSB1K3-T25, pSB1C3-T18-Zip + pSB1K3-T25, pSB1C3-T18-Zip + pSB1K3-T25 and pSB1C3-T18-Zip + pSB1K3-T25-Zip.

Our goal was to screen for peptide aptamers using a bacteria-based system. This system can be used to study protein-protein interactions. We used the bacterial two-hybrid system which is based on the reconstitution of the adenylate cyclase. In order to detect the rise in intracellular cAMP we used a RFP reporter system with a cAMP-activated promoter, PcstA. Valitadion of a functional two-hybrid system and characterization of the reporter system was needed, before we could screen for peptide aptamers.

Characterization of promotor PcstA,was done by meassuring levels of mRNA during growth. The promoter is sensitive to the glucose concentrations.

To validate if the main components of the "Two-hybrid System", T18 and T25 can be used to study protein-protein interactions, a control experiment set up, where the leucine zipper region from the GCN4 yeast (Saccharomyces cerevisiae) protein were fused to the T18 and T25 domains (T18-Zip+T25-Zip). As leucine zippers form homodimers, their interaction should lead to functional complementation between T18 and T25.

We used the E.coli K12 BTH101-strain, which is deficient in the gene encoding adenylate cyclase, cyaA. Our results showed that only when leucine zippers was fused to both T18 and T25, complementation was observed.

17 parts were sent to the Parts Registry. In Submitted Parts you can browse through our parts and be redirected to the Parts Registry. Where you will find more information for each parts.

This year we participated in iGEM's Second Internation InterLab Measurement Study. The goal of this study was to measure fluorescence from three different devices expressing GFP. We were able to measure the fluorescence of these devices using FACS. The data we acquired showed that there was a relative difference in promoter activity in the mutated promoters compared to the wild type.