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

(Abstract: biotINK - rethINK tissue printing)
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==<span style="color:#000000">Abstract:</span> <span style="color:#009440">biot</span><span style="color:#3070b3">INK</span> <span style="color:#8d8d8d">- rethINK tissue printing</span>==
 
==<span style="color:#000000">Abstract:</span> <span style="color:#009440">biot</span><span style="color:#3070b3">INK</span> <span style="color:#8d8d8d">- rethINK tissue printing</span>==
We are living in an aging society that is facing a decreasing supply of donor organs. To confront this pressing issue, w e developed a game-changing approach to
+
We are living in an aging society that is facing a decreasing supply of donor organs. To confront this pressing issue, we developed a game-changing approach to bioprint tissues for biomedical applications. Our interdisciplinary w ork aims to create a unique ink, named biotINK, to revolutionize bioprinting. The printing process uses a hijacked 3D printer and two components of biotINK to induce an instantaneous polymerization reaction, creating three-dimensional multi-cellular structures in a user-definable manner. The principle of this two-component glue relies on the rapid and specific interaction of biotin and its tetrameric binding protein, avidin. To employ the high biotin-avidin affinity, w e engineered cells presenting biotin moieties or biotin-binding proteins on their surfaces, as well as recombinant matrix proteins, which both co-polymerize upon printing. Furthermore, w e explored different genetic circuits which allow us to functionalize the bio-synthetic tissue and install biosafety mechanisms. Altogether, we are confident that our system provides the necessary means to advance the SynBio community to the next level – the tissue level.<br>
bioprint tissues for biomedical applications. Our interdisciplinary w ork aims to create a unique ink, named biotINK, to revolutionize bioprinting. The printing process
+
uses a hijacked 3D printer and two components of biotINK to induce an instantaneous polymerization reaction, creating three-dimensional multi-cellular structures in
+
a user-definable manner. The principle of this tw o-component glue relies on the rapid and specific interaction of biotin and its tetrameric binding protein, avidin. To
+
employ the high biotin-avidin affinity, w e engineered cells presenting biotin moieties or biotin-binding proteins on their surfaces, as w ell as recombinant matrix proteins,
+
which both co-polymerize upon printing. Furthermore, w e explored different genetic circuits which allow us to functionalize the bio-synthetic tissue and install
+
biosafety mechanisms. Altogether, w e are confident that our system provides the necessary means to advance the SynBio community to the next level – the tissue
+
level.<br>
+
 
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[[File:Muc_Finalsphoto_001.png|center|950px]]
 
<html><video width="830" controls><source src="https://static.igem.org/mediawiki/2016/6/64/Muc16_video3.mp4">
 
<html><video width="830" controls><source src="https://static.igem.org/mediawiki/2016/6/64/Muc16_video3.mp4">

Revision as of 17:13, 16 November 2016

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2016/11/02: We will update our wiki within the next 10 days. Please do not hesitate to contact us at iGEM2016.Munich@gmail.com.

Abstract: biotINK - rethINK tissue printing

We are living in an aging society that is facing a decreasing supply of donor organs. To confront this pressing issue, we developed a game-changing approach to bioprint tissues for biomedical applications. Our interdisciplinary w ork aims to create a unique ink, named biotINK, to revolutionize bioprinting. The printing process uses a hijacked 3D printer and two components of biotINK to induce an instantaneous polymerization reaction, creating three-dimensional multi-cellular structures in a user-definable manner. The principle of this two-component glue relies on the rapid and specific interaction of biotin and its tetrameric binding protein, avidin. To employ the high biotin-avidin affinity, w e engineered cells presenting biotin moieties or biotin-binding proteins on their surfaces, as well as recombinant matrix proteins, which both co-polymerize upon printing. Furthermore, w e explored different genetic circuits which allow us to functionalize the bio-synthetic tissue and install biosafety mechanisms. Altogether, we are confident that our system provides the necessary means to advance the SynBio community to the next level – the tissue level.

Muc Finalsphoto 001.png

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LMU & TUM Munich

Technische Universität MünchenLudwig-Maximilians-Universität München

United team from Munich's universities

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iGEM Team TU-Munich
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