Team:Utah State/Results

How our system works

In looking at the registry we found the AMP LL37 which is commonly found in Humans. Unfortunately the previous iterations of LL37 were not suitable for our purposes (either lacking a start codon: BBa_K245114, or not RFC 23, BBa_K875009 was RFC10). We decided to construct our own LL37 with RFC 23 under consideration as well as adding a star codon.
All other AMPs were new to the registry (and all submitted). These AMPs were also designed under the same parameters set forth in the LL37 (addition of start codon, and RFC23). It should be mentioned that all AMPs were codon optimized for expression in E. coli.

All AMPs were first cloned in front of a 10x His-Tag (BBa_K844000) and double terminator (BBa_B0015). A promoter and rbs was added to the construct to have a complete AMP production system.

After growing cells and purifying protein (see protocols page), SDS-PAGE gels were run with the elution fraction of each AMP from the nickel column. After coomassie staining and de-staining it was found that it was too hard to see the if there was any AMP expression as the final AMP products were so small.

The next step was to fuse the AMPs with GFP at the C-terminal. Since the AMPs were designed with RFC 23 under consideration creating a AMP-GFP fusion would not be an issue. Having GFP at the C-terminal means that if fluorescence is seen then AMPs were being expressed. In addition to fluorescence we wanted to try and purify AMP-GFP protein. This led to the creation/modification of an existing GFP to remove the stop codons (BBa_K1162011). The removal of the stop codon enabled the fusion of a C-terminal His-Tag to the end of the GFP. Protein purification was carried out using 0.2 mL Nickel columns.

The image above demonstrates that there is expression of LL37 and WAM in E c.oli as demonstrated by GFP fluorescence (GFP is at the C-terminal end). Unfortunately there were issues with binding to the Nickel column which will be troubleshooted in future work.

To demonstrate that antimicrobial spider silk could be manufactured in E. coli, the AMP LL-37 (BBa_K1162006) was fused to 8 repeats of spider silk (BBa_K844004. A lac inducible promoter system (BBa_K208010), 10x His Tag (BBa_K844000), and double terminator (BBa_B0015) were added to create the first antimicrobial spider silk generator with BioBricks.

The schematic below demonstrates the experimental process for validating and manufacturing of of AMP-spider silk fused proteins. As an example, the LL37-spider silk construct (BBa_K1162306) was chosen for expression studies (other AMP-spider silk constructs are listed on the BioBrick page). First 50 mL cultures were used to grow up bacteria containing LL37-spider silk. Protein was purified using a 0.2 mL nickel column and protein gel was run with: cell lysate, flow through, wash, and elution fractions. Gel from 50 mL culture did not show any evidence to suggest protein expression.

Next we decided to scale up the process to a 500 mL culture, purify on a 3 mL nickel column and carry out the protein analysis again (similar to 50 mL culture). We hypothesized that maybe our expression levels were low and proceeded to a 10 L fermentation and purified the protein on a 5 mL nickel column. The results of the 10L fermentation are shown in the gel below. In the elution fraction of the gel image below, we can see a protein band at approximately 55-60 kDa that is the size of the LL37-silk protein. From this study we have demonstrated that antimicrobial spider silk can be produced in E. coli and scale-up. Since we also have additional AMP-spider silk constructs(see BioBricks page for a complete list), the next step would be to manufacture more of them using a similar approach to LL37-spider silk. Furthermore, in future work, optimization of LL37-spider silk production would also need to take place.

Text descriptions go here.

To demonstrate that the N-terminal 10x His Tag (BBa_K1162009) functions correctly, it was cloned in front of Green Florescent Protein (GFP)with the lac promoter+rbs system (BBa_K208010)to give the complete construct BBa_K1162013. This construct was expressed in E. coli grown in 50mL LB media with the addition of chloramphenicol and induced with IPTG. After allowing to grow overnight the cells were spun down and protein was purified with a nickel spin column (see protein purification protocol on protocols page). Fractions from this nickel spin column procedure were saved and run on an SDS-PAGE gel (see below). Since this was a GFP purification procedure, the different fractions were dotted on parafilm and place on a UV gel box to visualize the protein (see below).

From the SDS-PAGE gel it can be seen that there is pure GFP (~26.9 kDa) in the elution fraction number 2 and 3. The wash fractions do not appear to have any GFP which indicates that the N terminal 10x His Tag is strongly bound to the Nickel Column during washing steps. Coupled with the GFP dot image it is clear that this method of purification works as desired and adds another purification system to the registry.

After demonstration that the N-terminal purification system functioned as desired, other constructs can be built to purify protein using this method.

To visually monitor the structures of AMPs, amino acid sequences were entered into the Protein Homology/analogY Recognition Engine (PHYRE2,Protein structure prediction on the web: a case study using the Phyre server Kelley LA and Sternberg MJE. Nature Protocols 4, 363 - 371 (2009),http://www.sbg.bio.ic.ac.uk/~phyre2/html/page.cgi?id=index). Output for each of the AMPs used by Utah State iGEM 2013 team is given below. Note: Grammistin (BBa_K1162003) was too small to model with this program. Interestingly when amino acid sequence for each AMP was entered into the program fused with 10x Histag, no change was seen the in the protein structure.