Difference between revisions of "Team:Paris Bettencourt"

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<div id="projectdescription">
 
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<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/9/9f/LogobiomatPB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/6/61/RochePB.gif"></div><h4>Biomaterials</h4>Three different biomaterials with differing/distinct properties were developed on: Calcium Carbonate, Polysilicate and P3HB. Each material has unique properties and differing applications, allowing for a broad spectrum of fields that the 3D printer belongs to.</div>
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<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/2/2c/RocheinertePB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/6/61/RochePB.gif"></div><h4>Biomaterials</h4>Three different biomaterials with differing/distinct properties were developed on: Calcium Carbonate, Polysilicate and P3HB. Each material has unique properties and differing applications, allowing for a broad spectrum of fields that the 3D printer belongs to.</div>
 
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<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/b/bc/LogolaserPB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/a/ad/LaserPB.gif"></div><h4>Light control</h4>Optogenetics allows fully reversible control of gene expression in both time and space. Both photosensory transmembrane proteins as well as photoswitchable protein caging were developed to expand the existing library of optogenetic tools.</div>
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<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/5/51/LaserinertePB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/a/ad/LaserPB.gif"></div><h4>Light control</h4>Optogenetics allows fully reversible control of gene expression in both time and space. Both photosensory transmembrane proteins as well as photoswitchable protein caging were developed to expand the existing library of optogenetic tools.</div>
 
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<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/2/28/LogoRNAPB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/e/ec/RNAtlogoPB.gif"></div><h4>RNA Agglomerations</h4>RNA is a light cost nucleotide material in the cell, which has potential to act as a scaffold and transporter. We aim to recreate RNA agglomerations as formed in mammalian cells with triple repeat disorders, which show liquid phase separation, forming a organelle-like vesicle, where local concentrations of enzymes can be created.</div>
 
<img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/2/28/LogoRNAPB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/e/ec/RNAtlogoPB.gif"></div><h4>RNA Agglomerations</h4>RNA is a light cost nucleotide material in the cell, which has potential to act as a scaffold and transporter. We aim to recreate RNA agglomerations as formed in mammalian cells with triple repeat disorders, which show liquid phase separation, forming a organelle-like vesicle, where local concentrations of enzymes can be created.</div>

Revision as of 23:26, 28 October 2017

BRINGING CONTROL TO THE
THIRD DIMENSION

Proof of concept - 3D printer: by creating a printer, it is a clear and easily quantified way to validate our 3D controls. It also allowed us to engineer biomaterials that would be compatible and useful in biotech. We also optimised production by creating local concnetrations of enzymes in the RNA organelles.
By creating logic circuits with photo sensitive proteins, we control and study cells in 3D.

Biomaterials

Three different biomaterials with differing/distinct properties were developed on: Calcium Carbonate, Polysilicate and P3HB. Each material has unique properties and differing applications, allowing for a broad spectrum of fields that the 3D printer belongs to.

Light control

Optogenetics allows fully reversible control of gene expression in both time and space. Both photosensory transmembrane proteins as well as photoswitchable protein caging were developed to expand the existing library of optogenetic tools.

RNA Agglomerations

RNA is a light cost nucleotide material in the cell, which has potential to act as a scaffold and transporter. We aim to recreate RNA agglomerations as formed in mammalian cells with triple repeat disorders, which show liquid phase separation, forming a organelle-like vesicle, where local concentrations of enzymes can be created.

Centre for Research and Interdisciplinarity (CRI)
Faculty of Medicine Cochin Port-Royal, South wing, 2nd floor
Paris Descartes University
24, rue du Faubourg Saint Jacques
75014 Paris, France
bettencourt.igem2017@gmail.com