Difference between revisions of "Team:Bielefeld-CeBiTec/Results/Library/Phage"

Line 27: Line 27:
 
<figure class="figure">
 
<figure class="figure">
 
   <img src="https://static.igem.org/mediawiki/2016/0/07/Bielefeld_CeBiTec_2016_10_18_LIB_Phagemid_formula.png" class="figure-img" width="45%" alt="">
 
   <img src="https://static.igem.org/mediawiki/2016/0/07/Bielefeld_CeBiTec_2016_10_18_LIB_Phagemid_formula.png" class="figure-img" width="45%" alt="">
−
   <figcaption class="figure-caption"><b>Figure 2: Agar plate, showing <i>E. coli</i> ER2738 colonies after one panning round of phagemid display.</b> Every colony carries a phagemid with the CDS for a Monobody with binding affinity to FGE protein</figcaption>
+
   <figcaption class="figure-caption"><b></figcaption>
 
</figure>
 
</figure>
 
<div class="container text">  
 
<div class="container text">  
 
<br>
 
<br>
−
We gained a concentration of 2.99x10<sup>13</sup> of Monobody carrying phages per mL and 1.599x10<sup>13</sup> of Nanobody carrying phages per mL in an elution volume of 1.5 mL each.  
+
We gained a concentration of 2.99 x 10<sup>13</sup> of Monobody carrying phages per mL and 1.599 x 10<sup>13</sup> of Nanobody carrying phages per mL in an elution volume of 1.5 mL each.  
  
 
<br>
 
<br>
 
These phages were used to accomplish one stage of phage panning on immuno-tubes, coated with several different proteins, from transcription factors to enzymes and protein domains. We explicit relinquished further panning rounds, to simulate the conditions of our system. Thereby just an initial binder is required to get optimized by <i>in vivo</i> mutation and selection. After an exhaustive washing procedure and the following elution of phages with affinity imparting binding proteins an exponential growing culture of ER2738 was infected and plated on LB agar, containing chloramphenicol.  
 
These phages were used to accomplish one stage of phage panning on immuno-tubes, coated with several different proteins, from transcription factors to enzymes and protein domains. We explicit relinquished further panning rounds, to simulate the conditions of our system. Thereby just an initial binder is required to get optimized by <i>in vivo</i> mutation and selection. After an exhaustive washing procedure and the following elution of phages with affinity imparting binding proteins an exponential growing culture of ER2738 was infected and plated on LB agar, containing chloramphenicol.  
−
After incubation at 37°C, several colonies were detectable on agar plates of all used target proteins.
+
After incubation at 37°C, several colonies were detectable on agar plates of all used target proteins (Fig. 1).
 
  </div>
 
  </div>
 
<figure class="figure">
 
<figure class="figure">
 
   <img src="https://static.igem.org/mediawiki/2016/b/ba/Bielefeld_CeBiTec_2016_10_18_LIB_Phagemid_Platte.png" class="figure-img" width="45%" alt="">
 
   <img src="https://static.igem.org/mediawiki/2016/b/ba/Bielefeld_CeBiTec_2016_10_18_LIB_Phagemid_Platte.png" class="figure-img" width="45%" alt="">
−
   <figcaption class="figure-caption"><b>Figure 2: Agar plate, showing <i>E. coli</i> ER2738 colonies after one panning round of phagemid display.</b> Every colony carries a phagemid with the CDS for a Monobody with binding affinity to FGE protein</figcaption>
+
   <figcaption class="figure-caption"><b>Figure 1: Agar plate, showing <i>E. coli</i> ER2738 colonies after one panning round of phagemid display.</b> Every colony carries a phagemid with the CDS for a Monobody with binding affinity to FGE protein</figcaption>
 
</figure>
 
</figure>
−
<div class="container text">As an example, we isolated and sequenced one of the Monobody CDSs coding for a formylglycine-generating enzyme (FGE) binder (Figure 2).
+
<div class="container text">As an example, we isolated and sequenced one of the Monobody CDSs coding for a formylglycine-generating enzyme (FGE) binder (Fig.&nbsp;2).
 
  </div>
 
  </div>
 
<br>
 
<br>

Revision as of 17:17, 19 October 2016



Library Results

Phagemid Display

Screening the Initial Diversity


The core of our system is the combination of an initial library with a mutation system and a selection system, to optimize Evobodies by directed evolution. To get in this evolutional process, some binding proteins must show at least a marginal affinity to the chosen target protein. Low affinity binders than get mutated and selected in vivo during the replication under a rising selective pressure.
To make sure, that the designed binding proteins are able to attach target proteins and the initial libraries containing some compatible Monobodies and Nanobodies, we performed a phagemid display, using phagemid pAK100 and M13 derived helper phages. (Link to protocol)

After assembling the pAK100 backbone with the CDS of our designed bindng proteins via Gibson cloning, the phagemid was transformed into electrocompetent E. coli ER2738 and plated on LB agar, containing chloramphenicol and tetracycline. Thus, we generated a comparative small library of about 3000 clones for each, Monobody and Nanobody coding phagemids, as test library for use in phagemid display.
Infecting the eluted and incubated culture with M13 derived helper phages and the following purification of the composed phages leads to pelleted phages, diluted in PBS. The UV-VIS absorbance of an 1:50 aliquot at 269 nm and 320 nm was measured, to calculate the phage concentration, based on the following formula:

We gained a concentration of 2.99 x 1013 of Monobody carrying phages per mL and 1.599 x 1013 of Nanobody carrying phages per mL in an elution volume of 1.5 mL each.
These phages were used to accomplish one stage of phage panning on immuno-tubes, coated with several different proteins, from transcription factors to enzymes and protein domains. We explicit relinquished further panning rounds, to simulate the conditions of our system. Thereby just an initial binder is required to get optimized by in vivo mutation and selection. After an exhaustive washing procedure and the following elution of phages with affinity imparting binding proteins an exponential growing culture of ER2738 was infected and plated on LB agar, containing chloramphenicol. After incubation at 37°C, several colonies were detectable on agar plates of all used target proteins (Fig. 1).
Figure 1: Agar plate, showing E. coli ER2738 colonies after one panning round of phagemid display. Every colony carries a phagemid with the CDS for a Monobody with binding affinity to FGE protein
As an example, we isolated and sequenced one of the Monobody CDSs coding for a formylglycine-generating enzyme (FGE) binder (Fig. 2).

Figure 2: Example Monobody, identified as FGE binder by phagemid display. Top to bottom: Ordered sequence, chromatogram and sequencing result.

Summarized, the phagemid display was a good opportunity, to screen our Monobody and Nanobody libraries at initial binding proteins for our directed evolution system. We could show, that in a small extract of 3.000 variable Monobodies, as well as Nanobodies, out of a theoretical library size of about 1 billion CDS contains some potential candidates for getting an Evobody!