Difference between revisions of "Team:Imperial College/Mechanisms"

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                 <p2>Redox molecules are maintained in a reduced form in ambient conditions. Application of a +0.5V potential oxidises the redox molecules, allowing for activation of the genetic circuit. Application of a -0.3V potential ensures the redox molecules remain reduced, preventing activation of the genetic circuit.</p2>
 
                 <p2>Redox molecules are maintained in a reduced form in ambient conditions. Application of a +0.5V potential oxidises the redox molecules, allowing for activation of the genetic circuit. Application of a -0.3V potential ensures the redox molecules remain reduced, preventing activation of the genetic circuit.</p2>
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                 <p2>Oxidised redox molecules oxidise the transcription factor SoxR. This allows it to bind to and initiate transcription from the pSoxS promoter. This allows for the electronic induction of any gene placed downstream of this promoter.</p2>
 
                 <p2>Oxidised redox molecules oxidise the transcription factor SoxR. This allows it to bind to and initiate transcription from the pSoxS promoter. This allows for the electronic induction of any gene placed downstream of this promoter.</p2>
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                     <p2>In ambient conditions or at -0.3V sulfite maintains pyocyanin in a reduced state whereas ferrocyanide is stable in its reduced form. The SoxR transcription factor therefore remains reduced, preventing induction of gene transcription from the pSoxS promoter.</p2>
 
                     <p2>In ambient conditions or at -0.3V sulfite maintains pyocyanin in a reduced state whereas ferrocyanide is stable in its reduced form. The SoxR transcription factor therefore remains reduced, preventing induction of gene transcription from the pSoxS promoter.</p2>
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                     <p2>An electrode pulse of +0.5V oxidises the redox molcules pyocyanin and ferrocyanide. Pyocyanin oxidises the SoxR transcription factor which in turn initiates transcription of any gene downstream of pSoxS. This electronic induction of gene expression is amplified by the oxidised ferricyanide which pulls electrons out of the respiratory transport chain.</p2>
 
                     <p2>An electrode pulse of +0.5V oxidises the redox molcules pyocyanin and ferrocyanide. Pyocyanin oxidises the SoxR transcription factor which in turn initiates transcription of any gene downstream of pSoxS. This electronic induction of gene expression is amplified by the oxidised ferricyanide which pulls electrons out of the respiratory transport chain.</p2>
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Revision as of 05:08, 17 October 2018


Design

Design Overview

PixCell is a major improvement on an existing electrogenetic system, making it aerobic, more responsive and fully modular. The system depends on a complex network of electrochemical, chemical and biomolecular interactions.

Electrochemical Module Design

Redox molecules are maintained in a reduced form in ambient conditions. Application of a +0.5V potential oxidises the redox molecules, allowing for activation of the genetic circuit. Application of a -0.3V potential ensures the redox molecules remain reduced, preventing activation of the genetic circuit.

Potentiostat:

The controller of the system. It generates either a +0.5V (ON) or -0.3V (OFF) current in the electrodes.

Electrode or Electrode Array:

The electrode is the driving force of the system. It allows for oxidation and reduction of redox molecules.

Pyocyanin:

This is a redox-cycling molecule produced by Pseudomonas aeuriginosa. In its oxidised form it can activate gene transcription of redox-signalling pathways, either directly or by oxidative stress. In normal aerobic conditions it is oxidised.

Ferrocyanide/Ferricyanide:

These molecules are well known redox mediators. The oxidised form (ferrocyanide) can draw electrons from the cells quinone pool. This amplifies the activity of redox-cycling molecules like pyocyanin. When the reduced form (ferricyanide) is present the opposite is true.

Sodium Sulfite:

This is an oxygen scavenger as it removes oxygen from solution. This allows for pyocyanin to be maintained in a reduced form but does not diminish GFP fluorescence, suggesting cells remain in aerobic conditions.

Biological Module Design

Oxidised redox molecules oxidise the transcription factor SoxR. This allows it to bind to and initiate transcription from the pSoxS promoter. This allows for the electronic induction of any gene placed downstream of this promoter.

SoxR:

SoxR is a transcription factor which is constitutively expressed from the pSoxR portion of the pSoxR/pSoxS bidirectional promoter. Upon oxidation by a redox-cycling drug (such as pyocyanin) SoxR is able to activate gene transcription downstream of the pSoxS portion of the bidirectional promoter. The PixCell library contains a series of SoxR transcription factors with different activities which can be assembled modularly.

pSoxS:

pSoxS forms one half of the pSoxR/pSoxS bidirectional promoter. It is constitutively inactive, being activated by oxidised SoxR. The PixCell library includes engineered, unidirectional pSoxS promoters with variable activity which can be assembled modularly.

Quinone Pool:

Quinones are molecules found in respiratory membranes which shuttle electrons across the electron transport chain. Ferricyanide has been known to oxidise the quinone pool, drawing electrons out of a cell to amplify the response of pyocyanin. The full mechanism of this pathway is currently unknown.

PixCell Electrogenetic System Design

In ambient conditions or at -0.3V sulfite maintains pyocyanin in a reduced state whereas ferrocyanide is stable in its reduced form. The SoxR transcription factor therefore remains reduced, preventing induction of gene transcription from the pSoxS promoter.
An electrode pulse of +0.5V oxidises the redox molcules pyocyanin and ferrocyanide. Pyocyanin oxidises the SoxR transcription factor which in turn initiates transcription of any gene downstream of pSoxS. This electronic induction of gene expression is amplified by the oxidised ferricyanide which pulls electrons out of the respiratory transport chain.