Team:TU Eindhoven/Achievements/Submitted Parts/COMPx

COMPx

Usage and Biology

CPX, or Circularly permuted OmpX, was developed as a bacterial display methodology for N- and C- terminal display. It has been shown to enable rapid screening of very large peptide libraries with high precision and efficiency. OmpX possesses four extracellular loops, with loops 2 and 3 forming a semi rigid β-sheets protruding from the cell surface. The native N- and C-termini were fused together by a GGSG linker, and the newly formed N and C termini reside on the cell surface.

CPX was created by Rice et al1 as a scaffold for peptide libraries. Rice et al added a part at the N terminus that is used for the random mutation needed for Peptide Libraries. Furthermore Rice et al shows that CPX can easily be overexpressed without effecting the cell growth or cell viability. This makes CPX a very useful protein for any type of displaying.

Gene Design

To integrate a Non-natural amino acid in the sequence of CPX some modifications were made. Within the part in which originally random mutations were induced a codon was mutated into the amber stop codon TAG. With a specific tRNA it is possible to implement a Non-Natural amino acid at the place of the TAG codon. The TAG codon was introduced into the Peptide Library by Site-Directed Mutagenesis. A HA-tag was also added to the C-terminus of the protein using overhang primers to use in characterization. After the modifications the protein was renamed to Clickable Outer Membrane Protein X (COMPx).

Characterization

Team TU_Eindhoven 2014 tried to create a membrane anchor to which molecules could covalently bind. With this protein it is possible to bind anything to the membrane by using a bio-orthogonal “click” reaction. To test the functionality of the protein several assays were done.

For all the assays we used the following vectors pET29a COMPx (Membrane Protein) and pEVOL-PylT-2xTyrRS. (tRNA, tRNA synthetase). Both vectors were transformed into BL21(DE3) strain. Colonies of this transformation were grown on LB. After culturing, glycerol stocks were made. All the assays were done by culturing the bacteria from this glycerol stock. Check our Protocol Page for all the protocols of TU Eindhoven 2014.

Antibody Confirmation

First assay done was to confirm that the protein was expressed on the membrane. This was done by adding an anti-HA antibody labeled with TAMRA dye to bacteria in solution that had been expressing COMPx. The bacteria were then analyzed with FACS. Results show that COMPx is expressed on the membrane of the bacteria (Figure 3). For the used protocol see Antibody Labeling.

DBCO-PEG4-TAMRA Confirmation

Now that it is proven that the protein is expressed on the membrane the next step can be taken. This assay is to see whether or not the non-natural amino acid is being incorporated into COMPx. For labeling DBCO-PEG4-TAMRA was used. If the non-natural amino acid is present in the protein then DBCO-PEG4-TAMRA should be measured after washing steps. DBCO-PEG4-TAMRA was added in two different concentrations, in excess, to bacteria in solution that had been expressing COMPx. The bacteria were then analyzed with FACS. Data clearly shows that DBCO-PEG4-TAMRA is still on the membrane after washing steps. (Figure 4) Therefore it was concluded that the DBCO of the dye is clicked to the Azide, in other words: the dye has covalently bound to the protein. For the used protocol see FACS sorting with DBCO-PEG(10kDa) and FACS sorting with DBCO-TAMRA.

Anti-Body Titration

In order to verify expression of our designed outer membrane protein COMPx and to obtain further insight the degree of expression, we performed an antibody titration. Out of this titration a K_d can be calculated if the upper and lower plateau is measured. With the K_d it is possible to calculate the number of anchors on the membrane. This was an important assay for the TU Eindhoven 2014 team to determine how many binding sites there were per bacteria. For this titration several concentration of anti-HA antibody have been used. Bacteria have been analyzed with FACS. For the used protocol see Antibody Titration with FACS.

Unfortunately the upper plateau was not reached. Therefore it is not possible to calculate a K_d from this data. Reasons for this can be that the washing steps were not effective enough, or the protein is expressed in really high numbers.