Team:NYMU-Taipei/Our institute

From 2011.igem.org

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To achieve this goal, we use a species of magnetic bacteria, Magnetospirillum magneticum AMB-1. We have chosen mms13, a transmembrane protein as our target for protein design, as it serves as a linker between reception of wireless magnetic field and optogenetic neuro-stimulation output. Regarding the neuroimmune response, we choose three genes to achieve symbiosis within glial cell: ''MinC'', a division inhibitor, ''INV'', a gene for invasion and ''LLO'', a gene for facilitated escape from phagosomes.</font>
To achieve this goal, we use a species of magnetic bacteria, Magnetospirillum magneticum AMB-1. We have chosen mms13, a transmembrane protein as our target for protein design, as it serves as a linker between reception of wireless magnetic field and optogenetic neuro-stimulation output. Regarding the neuroimmune response, we choose three genes to achieve symbiosis within glial cell: ''MinC'', a division inhibitor, ''INV'', a gene for invasion and ''LLO'', a gene for facilitated escape from phagosomes.</font>
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*'''<font size=3>Our design is made up of following two devices:</font>'''<br>
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<font size=2>
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*[https://2011.igem.org/Team:NYMU-Taipei/optomagnetic-design Optomagnetic Design]
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**The bridge of magnetic and optogenetic
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*[https://2011.igem.org/Team:NYMU-Taipei/immunological-solution Immunological Solution]
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**Make magnetic bacteria symbiosis with glia cell
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</font>

Revision as of 13:05, 5 October 2011

  • Our design

To achieve this goal, we use a species of magnetic bacteria, Magnetospirillum magneticum AMB-1. We have chosen mms13, a transmembrane protein as our target for protein design, as it serves as a linker between reception of wireless magnetic field and optogenetic neuro-stimulation output. Regarding the neuroimmune response, we choose three genes to achieve symbiosis within glial cell: MinC, a division inhibitor, INV, a gene for invasion and LLO, a gene for facilitated escape from phagosomes.

  • Our design is made up of following two devices:

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