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

Line 12: Line 12:
 
</ul>
 
</ul>
 
<article>
 
<article>
<h2>Abstract: BiotINK – Rethink tissueprinting</h2>
+
<h2>Abstract: BiotINK – rethINK tissueprinting</h2>
 
<p>
 
<p>
In the present decade, the possibilities enabled by 3D printing and scanning have led to an industrial revolution in
+
Living in an aging society and facing the concomitant organ shortage, we have developed a game-changing approach to bioprint tissues for biomedical application. Our interdisciplinary work entails creating a novel bioink that exploits the rapid and specific interaction of biotin and its tetrameric binding protein streptavidin. By employing this affinity, we have engineered cells presenting biotin moieties or biotin binding proteins on their surfaces and recombinant biotinylated proteins as spacer molecules, which both co-polymerize upon contact with streptavidin. Furthermore, we have explored different cellular circuits, which allow us to control pancreatic cell lines, induce tissue vascularization, or install biosafety mechanisms for printed tissues. To deliver these cells, we employ a hijacked 3D printer that enables us to manufacture three-dimensional multi-cellular structures in a user-definable manner. <br>
prototyping and the production industry as well as in households. Predictably, this new way of simple, tailored fabrication
+
Altogether, we are confident that our system provides the necessary means to advance the SynBio community to the next level – the tissue level.
will have an enormous impact when applied to the fields of personalized medicine and synthetic biology. Bio-printing
+
has the potential to meet the huge global demand for replacement organs and therefore to greatly increase the life quality of
+
elderly people.<br><br>
+
Successfully developing bio-printing requires a strongly interdisciplinary team for a harmonized development, including: i) bio-printers with special print heads, ii) BioInk composed of proteins providing mechanical stability, and iii) cells that need
+
to be understood, engineered and adapted by means of Synthetic Biology.
+
We will transform an affordable household 3D printer into a bio-printer for Synthetic Biology applications. This includes engineering a printhead for bioprinting and adapting the 3D printer software, through which bioprinters will be made accessible for a broad scientific community.<br><br>
+
Additionally, our team has developed a new BioInk that is based on the ability of proteins to specifically interact with their clients: The challenge is to develop a BioInk that remains fluid in the printhead and will rapidly assemble when printed to provide mechanical stability. Our new approach utilizes the affinity between biotin and the biotin-binding proteins streptavidin and avidin - the strongest non-covalent interaction in biology. In employing this tight molecular interaction, our team has
+
designed an innovative dual-component “protein glue” (BioInk) that opens unprecedented opportunities for the field of
+
bio-printing.<br><br>  
+
Regarding the third main field, we will use genetically engineered cells for bio-printing. We have engineered tunable cellular
+
membrane proteins that allow the cells to interact with the surrounding matrix formed by our new BioInk. Subsequently, we will engineer functions into our printed cells that allow the printed tissue to be employed to treat different diseases. For a controlled release of these chosen therapeutic proteins, we have also used existing knowledge on optigenetics to render production of these therapeutic proteins inducible by illuminating the therapeutic implant
+
with a tissue-penetrating lamp.<br>
+
 
</p>
 
</p>
  

Revision as of 11:38, 15 August 2016

LMU and TU Munich 2016

Abstract: BiotINK – rethINK tissueprinting

Living in an aging society and facing the concomitant organ shortage, we have developed a game-changing approach to bioprint tissues for biomedical application. Our interdisciplinary work entails creating a novel bioink that exploits the rapid and specific interaction of biotin and its tetrameric binding protein streptavidin. By employing this affinity, we have engineered cells presenting biotin moieties or biotin binding proteins on their surfaces and recombinant biotinylated proteins as spacer molecules, which both co-polymerize upon contact with streptavidin. Furthermore, we have explored different cellular circuits, which allow us to control pancreatic cell lines, induce tissue vascularization, or install biosafety mechanisms for printed tissues. To deliver these cells, we employ a hijacked 3D printer that enables us to manufacture three-dimensional multi-cellular structures in a user-definable manner.
Altogether, we are confident that our system provides the necessary means to advance the SynBio community to the next level – the tissue level.

Sponsors