Team:Prairie View/Project

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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, and a lab notebook.  PLEASE keep all of your pages within your Team:Example namespace. 
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
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|align="center"|[[Team:Prairie_View | Team Example 2]]
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!align="center"|[[Team:Prairie_View/Notebook|Notebook]]
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(''Or you can choose different headings.  But you must have a team page, a project page, and a notebook page.'')
 
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== '''Overall project''' ==
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Our work is aimed at developing a biosensor for the detection of cations by introducing electron network system proteins into the chassy best suited to receive an enhanced energy flow. The flow of electrons is fueled through the network of oxidation reactions of bivalent metals across Ion channels and Cytochrome complexes. By facilitating the flow of electrons in a cell, we have showed an increase of ATP production. Bacterial cells use ATP for anabolic reactions, including the synthesis of DNA. Through our electron network system, we can enhance the expression of DNA, increasing cell replication along with the fluorescence of our reporters. Together, these incorporated proteins enhance the capacity of our sensor device.<br><br>
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Your abstract
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Our goal is to establish specificity within the sensing device. To accomplish this, we have selected new vectors (BSK and pET) and have designed primers to replicate the parts used in previous experiments along with the addition of cytochrome C. Our approach in designing these parts is to assemble ligations with a more modular construction enabling specificity in our sensor. We can now test with each metal alone and in combinations with and without Cytochrome C & Ion Channels.<br><br>
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Our testing system is designed for training a computer model with the data on an accept/reject basis. The targeted divalent cations are accepted by the model because their electrical configurations allow oxidation for the electron network system. Introduced anions will be used for rejected data because their valence decline oxidation and consequently will not produce the ATP/fluorescent values that the model is trained to accept. This accept/reject basis enhances the degree of specificity of our sensor and of the computational model.<br><br>
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To expand on this research, we would like to design our own proteins; new ion channels and cytochrome complexes that are specific to the electrical configurations of the target ions. These electrically gated proteins would discriminate passage based on the energy of the ion. This kind of project would involve a collaborative field effort and we are seeking cooperative interest.
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!align="center"|[[Team:Prairie_View|Home]]
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== Project Details==
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!align="center"|[[Team:Prairie_View/Team|The Team]]
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!align="center"|[[Team:Prairie_View/Project|The Project]]
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!align="center"|[[Team:Prairie_View/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Prairie_View/Modeling|Modeling]]
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!align="center"|[[Team:Prairie_View/Notebook|Notebook]]
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=== Part 2 ===
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=== The Experiments ===
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=== Part 3 ===
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== Results ==
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Latest revision as of 19:14, 29 October 2008

Prairie View iGEM.jpg
Home The Team The Project Parts Submitted to the Registry Modeling Notebook


Our work is aimed at developing a biosensor for the detection of cations by introducing electron network system proteins into the chassy best suited to receive an enhanced energy flow. The flow of electrons is fueled through the network of oxidation reactions of bivalent metals across Ion channels and Cytochrome complexes. By facilitating the flow of electrons in a cell, we have showed an increase of ATP production. Bacterial cells use ATP for anabolic reactions, including the synthesis of DNA. Through our electron network system, we can enhance the expression of DNA, increasing cell replication along with the fluorescence of our reporters. Together, these incorporated proteins enhance the capacity of our sensor device.

Our goal is to establish specificity within the sensing device. To accomplish this, we have selected new vectors (BSK and pET) and have designed primers to replicate the parts used in previous experiments along with the addition of cytochrome C. Our approach in designing these parts is to assemble ligations with a more modular construction enabling specificity in our sensor. We can now test with each metal alone and in combinations with and without Cytochrome C & Ion Channels.

Our testing system is designed for training a computer model with the data on an accept/reject basis. The targeted divalent cations are accepted by the model because their electrical configurations allow oxidation for the electron network system. Introduced anions will be used for rejected data because their valence decline oxidation and consequently will not produce the ATP/fluorescent values that the model is trained to accept. This accept/reject basis enhances the degree of specificity of our sensor and of the computational model.

To expand on this research, we would like to design our own proteins; new ion channels and cytochrome complexes that are specific to the electrical configurations of the target ions. These electrically gated proteins would discriminate passage based on the energy of the ion. This kind of project would involve a collaborative field effort and we are seeking cooperative interest.




Home The Team The Project Parts Submitted to the Registry Modeling Notebook
Retrieved from "http://2008.igem.org/Team:Prairie_View/Project"