Team:Toulouse-INSA-UPS/Demonstrate

DEMONSTRATE


The integration of our entrepreneurial and social analysis led us to consider finding a way to functionalize bacterial cellulose. For this purpose, we designed a three headed proteic platform that we named Cerberus in reference to the mythological dog. It is composed of a cellulose-binding molecular module (CBM3a) fused at its N-terminal part to a biotinylated molecule-binding head (monomeric streptavidin) and at its C-terminal part to an unnatural amino acid (UnAA) 4-azido-L-phenylalanine moiety. We also successfully set up a workflow allowing the synthesis of Cerberus (Figure 1).

Fluorescence Retained
Figure 1: Workflow of our Cerberus project experimental validation process.

Validation of the Three Binding Heads


Cellulose Binding


We designed a fusion protein between the Carbohydrate Binding Module type 3a and a fluorescent reporter and named it Sirius. Its purpose is to validate the association of our system towards cellulose. We demonstrated, using mRFP1 alone as negative control, the binding of our protein as showned in Figure 2. We were then confident in the binding of our protein to cellulose.

Fluorescence Retained
Figure 2: Picture of cellulose pull-down assay with mRFP1 alone (left tube) or with the Sirius construction (right tube)

Biotinylated compound affinity


Our second construction consisted on our Cerberus protein but lacking the unnatural amino acid. This construction aimed to prove the binding affinity of our system toward biotinylated compounds. As biotinylation can be both performed at high yield in vivo and in vitro, this construction is already a molecular binding plateform, allowing the purification of biotinylated compounds at low cost, using cellulose. We validated this construction using biotinylated mTag Blue Fluorescent Protein (Figure 3.a), biotinylated in vivo in E. coli.

Fluorescence Retained
Figure 3: Functionalization of cellulose with Orthos bound to biotinylated BFP. Fluorescence remaining on cellulose fraction after several washes (*Mann Whitney test p-value 0.01)

Click chemistry


Our plateform aims to have a binding capacity as wide as possible. The azide groupment offers a high efficiency covalent bound formation through cycloaddition reaction, mostyl known by Click chemistry. The possibilities offered by this system are therefore included in the unnatural amino acid : 4-azido-L-phenylalanine. We designed our protein to bear an Amber stop codon for unnatural amino acid integration in our plateform. We confirmed the activity of this integration using DBCO-Fluorescein as showed in figure 4.

Fluorescence Retained
Figure 4: Functionalization of cellulose with FITC conjugated to Cerberus. Fluorescence remaining in cellulose fraction after several washes (quadruplicate test). (*Mann Whitney test p-value 0.03)

Compounds Fuctionalization


Fluorescence


Once our system proved, we tried to associate several molecules in order to prove the system versatility. We successfully associate fluorescein to the streptavidin head. We made it possible thanks to the click chemistry with which we brought the necessary biotin for the streptavidin interaction.

Fluorescence Retained
Figure 1: Picture of functionalized cellulose under UV ligth with Sirius (CBM3a fused with mRFP1). Left: control mRFP1 alone; Right: Sirius

Color


Thanks to Sirius and its brightness, we could observe how the color remained on Bacterial Cellulose (figure 2) even after dozen of washes!

Fluorescence Retained
Figure 2: Picture of functionalized cellulose with Sirius (CBM3a fused with mRFP1). Left: control mRFP1 alone; Right: Sirius

Antibacterial Activity


We also conjugated an antimicrobial peptide, scygonadin, to the streptavidin, even if we need to optimize protocol (figure 3) we are comfident in the remaining biological activity after peptide binding on Cerberus.

Fluorescence Retained
Figure 3: Halo of inhibition of Orthos alone ( C), scygonadin alone (S) and Orthos+scygonadin (C+S) samples

Paramagnetism


For the AzF head, we decided to bind an inorganic molecule: paramagnetic beads, and it was a success (see the video below, figure 4). So our Cerberus platform has allowed us to make magnetic cellulose.

Figure 4: Video of the Cerberus-functionalized paramagnetic cellulose: on the left, control with paramagnetic beads alone; on the right, Cerberus-paramagnetic beads.

Versatility of the system


All of our experiments demonstrated the versatility of our system. Indeed, click chemistry is a real advantage to increase number of possibilities of functionalities. DBCO-biotin compound may be used as an adaptor between the streptavidin head and the AzF head as showed in figure 6.

Fluorescence Retained
Figure 6: Functionalization of cellulose with Orthos bound to in vitro-biotinylated FITC. Fluorescence remaining on cellulose pellet fraction after several washes (quadruplicate test). (*Mann Whitney test p-value 0.1)

Perspectives and conclusion


We successfully set up a workflow allowing the synthesis of Cerberus, a proteic platform that is composed of a cellulose-binding molecular module (CBM3a) fused at its N-terminal part to a biotinylated molecule-binding head (monomeric streptavidin) and at its C-terminal part to an unnatural amino acid (UnAA) 4-azido-L-phenylalanine moiety. Combining molecular modeling, synthetic biology and chemistry, we proved that Cerberus is a valuable and versatile platform allowing to functionalize cellulose with organic and inorganic compounds.

We can also plan to associate carbon nanotubes and graphene to AzF head in the aim to change cellulose fibre rigidity and create conductive cellulose, respectively. In order to do that, we successfully activated these compounds by diazotization reaction. The click chemistry assay and validation protocol need improvement to obtain our goal.

Bacterial cellulose has unique properties such as its natural purity may give it a bright future in the industries, that is why we decided to produce functionalized bacterial cellulose in vivo in reactor. As a first step towards the production of functionalized bacterial cellulose in a reactor, we demonstrate that CBM3a module of Cerberus fused to Red fluorescent protein is able to make bacterial cellulose fluorescent. Moreover, our first production of Orthos in Pichia pastoris are very conclusive, but we have to optimize the production.

Finally, we can also imagine to change our CBM3a to another proteic domain to associate functionalizing proteins to new materials as plastic to facilitate its degradation for example.