Difference between revisions of "Team:LMU-TUM Munich/Proof"

(Creating the perfect "sausage")
(Creating the perfect "sausage")
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The tests showed that the polymerization effect is only dependent on three things:
 
The tests showed that the polymerization effect is only dependent on three things:
* amount of cells/mL in the ink
+
* "cell density" in the biotINK
* concentration of BSA in the ink
+
* concentration of "BSA" in the biotINK
* concentration of Streptavidin inside the printing medium
+
* concentration of "Streptavidin" inside the printing medium
  
 
Since the addition or removal of biotinylated eGFP from the ink did not show a significant effect on then polymerization it was added to every sample for better visualization.
 
Since the addition or removal of biotinylated eGFP from the ink did not show a significant effect on then polymerization it was added to every sample for better visualization.

Revision as of 09:12, 19 October 2016

Muc16 Sticker Proof 001.png

Wichtiger Kommentar: Polymerization wird Proof-of-Principle page.

Introduction to polymerization

Design: Why we chose the Avidin & Biotin affinity pair

  • Vergleich mit anderen Polymerisationsmöglichkeiten die wir diskutiert hatten
  • Tabelle mit Literaturwerten zu Assoziationsraten
Properties of membrane proteins
Affinity pair Kind of interaction Dissociation constant Association rate Comment
Avidin - Biotin non covalent 10-15M [1] 55 440
SpyCatcher - SpyTag covalent not applicable
StrepTactin - Strep-tag II

Multivalency and avidity as major principles for polymerization

  • Strukturmodeling

Muc16-eGFP-annimatedGIF.gif Muc16-BSA-annimatedGIF.gif

Different polymers possible with biotINK polymerization

Since the foundation of our polymerization reaction is the interaction of Streptavidin and its binding partner Biotin (Referenz) we used biotinylated polymers to convery the polymerization between the cells.

  • Mesh-Bilder von Luisa

Results: Polymerization experiments

Creating the perfect "sausage"

In order to characterize our cells concerning their biotin binding capabilities by taking a look at their polymerization behaviour after adding them to a medium, which is rich of biotinylated protein linkers.

Since the expression of the two biotin binding receptor constructs was significantly higher than the expression of the biotin presenting one, we mainly used one of the biotin binding constructs, the scAvidin version. The main idea behind the polymerization experiments was that we wanted to find the perfect conditions for the cells to stick together, concerning the right medium, concentration and biotinylation degree of the protein linker.


The main components of all our polymerization experiments were svAvidin-construct-transfected Trex cells, biotinylated bovine serum albumine and streptavidin (or streptactin).

Our first experiments were not conducted with our printer, but under a fluorescence microscope for better analysability of the produced polymer.

The tests showed that the polymerization effect is only dependent on three things:

  • "cell density" in the biotINK
  • concentration of "BSA" in the biotINK
  • concentration of "Streptavidin" inside the printing medium

Since the addition or removal of biotinylated eGFP from the ink did not show a significant effect on then polymerization it was added to every sample for better visualization.

Experiments showed that the concentration of biotinylated BSa in our biotINK is the limiting factor for polymerization. The Higher the concentration of BSA was, the more structural integrity of the "printed" polymer could be oberved.

Negativ

After the

In the Micromanipulator










References

  1. Green, N. M. (1963). Avidin. 1. The use of [14C] biotin for kinetic studies and for assay. Biochemical Journal, 89(3), 585.

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LMU & TUM Munich

Technische Universität MünchenLudwig-Maximilians-Universität München

United team from Munich's universities

Contact us:

Address

iGEM Team TU-Munich
Emil-Erlenmeyer-Forum 5
85354 Freising, Germany