Team:Technion

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Latest revision as of 18:59, 18 October 2012

Our project, in short

Viruses can be described as complex 3D structures capable of efficient infection of their target organism. Because of their highly specific infection ability, they can be used as vessels for "smart" therapeutic strategies which rely on an agent that can effectively analyze the cellular environment and compute an appropriate response. To demonstrate the potential of a "smart" strategy, we are developing a "Trojan Horse" type of approach based on bactriophage-lambda.

Our project uses phage lambda and its target organism, E.coli, as a proof of concept for creating a system with predefined actions that demonstrates the described strategy. The design is based on a high specificity system which combines several different cell elements that will function as a type of logic AND gate. The phage will not harm the bacteria unless three independent conditions are met, activating the phage's lytic cycle and resulting in the bacteria's death; imitating a "Trojan Horse".
Read more about our project on the project description and project overview pages.

The reporter system standard

One of our main achievements was a reporter system standard. This standard was used to measure the expression of phage RNA polymerases (such as T7 RNA polymerase), which were an intermediate product in our system. The reporter system is composed of phage promoters followed by one of two reporter genes: alkaline phosphatase and xylE. These reporters expand the variety of reporter proteins beyond the commonly used fluorescent proteins, lacZ and luciferase. Read more about this standard here.

Our team

The pioneers

We are the first iGEM team from Israel and we are proud to represent the Technion in the competition. Make sure you read about our advisors, check out the team members and read about where we are from.

Human practice

As the pioneers of iGEM in Israel, we felt the need to reach out to the community. A few of us gave a lecture to senior year high school students from biology class. Read about the experience and check out the pictures here.

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-==Project description==
-Viruses can be described as complex three dimensional structures capable of efficient infection of their target organism. Because of their highly specific infection ability, they can be used as vessels for "smart" therapeutic strategies. Diseases such as cancer, diabetes, or any other autoimmune disease are a potential target for a therapeutic agent that can effectively analyze the cellular environment and compute an appropriate response. <br><br>
+==Our project, in short==
-To demonstrate the potential of a "smart" strategy, we are developing a "Trojan Horse" type of approach based on bactriophage lambda; an organism we dubbed "Trojan Phage". Our project uses phage lambda and its target organism, Escherichia coli, as a proof of concept for creating a system with predefined actions that demonstrates the described strategy. The design is based on a high specificity system that combines several different cell elements that will function as a type of logic AND gate. The phage will not harm the bacteria unless three independent conditions are met, activating the phage's lytic cycle and resulting in the bacteria's death; imitating a "Trojan Horse". <br><br>
+[[File:phage.jpg|thumb|border| right|text-bottom|300px|[https://2012.igem.org/Team:Technion/Project/Description <font size="4">Read more about our project</font>]]]Viruses can be described as complex 3D structures capable of efficient infection of their target organism. Because of their highly specific infection ability, they can be used as vessels for "smart" therapeutic strategies which rely on an agent that can effectively analyze the cellular environment and compute an appropriate response. To demonstrate the potential of a "smart" strategy, we are developing a "Trojan Horse" type of approach based on bactriophage-lambda.<br>
-The system design uses three logical buffer gates followed by the AND gate. The three buffer gates will be implemented as three specific protein interactions between the phage and the bacteria. At first, three polymerase enzymes will be produced by the bacteria in response to the presence of specific concentrations of inducers in the medium. The control over the production of the polymerase enzymes will be done by three independent systems, each consisting of a different promoter.  The first two will be based on the pTetO (induced by tetracycline) and pLac/Ara (induced by lactose and arabinose) promoters, the third one we intend to create ourselves by combining the pLux promoter (induced by an acyl homoserine lactone) with a theophylline induced riboswitch. Afterwards, the three polymerases will induce transcription from their matching promoters in the phage which will replace normal promoters controlling gene expression necessary for the phage's lytic life cycle. Thus, the phage will not complete its lytic cycle until all three factors in the host cell will activate it, allowing the three dimensional structure of the phage to assemble. <br><br>
+Our project uses phage lambda and its target organism, E.coli, as a proof of concept for creating a system with predefined actions that demonstrates the described strategy. The design is based on a high specificity system which combines several different cell elements that will function as a type of logic AND gate. The phage will not harm the bacteria unless three independent conditions are met, activating the phage's lytic cycle and resulting in the bacteria's death; imitating a "Trojan Horse".<br>
-The system we describe is a combined analogue - digital computational system. The  digital emerges from the 3-input AND gate to generate the output, and it is analogue, since the creation of the 3D structure requires the cooperation and coordination of all of the phage's cell components. The interaction between the digital and analogue components is self-determining; our role is only in the first step that "jump-starts" the system.<br><br>
+Read more about our project on the [https://2012.igem.org/Team:Technion/Project/Description project description] and [https://2012.igem.org/Team:Technion/Project/Overview project overview] pages.
-By creating a functional "Trojan Phage", we will have created a high specificity system composed of two different engineered living elements that interact causing a creation of a living output capable of self replication. This sort of system can be adapted to function as a therapeutic agent for a wide range of conditions.
+==The reporter system standard==
+One of our main achievements was a reporter system standard. This standard was used to measure the expression of phage RNA polymerases (such as T7 RNA polymerase), which were an intermediate product in our system. The reporter system is composed of phage promoters followed by one of two reporter genes: alkaline phosphatase and <em>xylE</em>. These reporters expand the variety of reporter proteins beyond the commonly used fluorescent proteins, <em>lacZ</em> and luciferase. Read more about this standard [https://2012.igem.org/Team:Technion/Project/Reporter here].
+[[File:Technion Team.JPG|thumb|400px|left|top|[https://2012.igem.org/Team:Technion/Team <font size="4">Our team</font>]]]
+==The pioneers==
+We are the first iGEM team from Israel and we are proud to represent the Technion in the competition. Make sure you read about our [https://2012.igem.org/Team:Technion/Team#Mentors_and_Advisers advisors], check out the [https://2012.igem.org/Team:Technion/Team#Our_Team_-_The_looks_and_the_brains team members] and read about [https://2012.igem.org/Team:Technion/Team#Where_we.27re_from where we are from].
+==Human practice==
+As the pioneers of iGEM in Israel, we felt the need to reach out to the community. A few of us gave a lecture to senior year high school students from biology class. Read about the experience and check out the pictures [https://2012.igem.org/Team:Technion/Human_Practices/High_School_Lecture here].
+[[File:TechnionBanner1.jpg|thumb|600px|center|]]