Team:Berkeley/Project/Overview

From 2010.igem.org

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This year our goal was to engineer <i>Escheria Coli</i> bacteria to serve as a vector for delivering proteins to the cytoplasms of phagocytotic eukaryotes. Our project focuses on the delivery of  GFP to the cytoplasm of choanoflagellates. (See [https://2010.igem.org/Team:Berkeley/Project/Motivation Motivation] for more information on choice of choanoflagellates). <br>
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This year our goal was to engineer <i>Escheria Coli</i> bacteria to serve as a vector for delivering proteins to the cytoplasms of phagocytic eukaryotes. Our project focuses on the delivery of  GFP to the cytoplasm of choanoflagellates. (See [https://2010.igem.org/Team:Berkeley/Project/Motivation Motivation] for more information on choice of choanoflagellates). <br>
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We are excited to report that we have been able to achieve successful delivery of GFP to the cytoplasms of choanoflagellates with a high rate of delivery!
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We are excited to report that we have been able to achieve successful delivery of GFP to the cytoplasms of choanoflagellates with a high rate of delivery! Visit our [https://2010.igem.org/Team:Berkeley/Results Results] page for more information. While we focused on delivery of GFP to choanoflagellates, we have built other more interesting [https://2010.igem.org/Team:Berkeley/Project/Payload Payloads] and we are working on delivering these and GFP to other eukaryotic [https://2010.igem.org/Team:Berkeley/Project/Other_organisms organisms].
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Visit our [https://2010.igem.org/Team:Berkeley/Results Results] page for more information. The design and execution of our project brought up issues of biosafety, which are discussed on our [https://2010.igem.org/Team:Berkeley/Project/Human_Practices Human Practices] page. In addition to the wet lab work outlined above, our team made significant improvements to the [https://2010.igem.org/Team:Berkeley/Clotho Clotho] software originally presented by the [https://2008.igem.org/Team:UC_Berkeley_Tools 2008 Berkeley iGEM Software team].
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The design and execution of our project brought up issues of biosafety, which are discussed on our [https://2010.igem.org/Team:Berkeley/Project/Human_Practices Human Practices] page. In addition to the wet lab work outlined above, our team made significant improvements to the [https://2010.igem.org/Team:Berkeley/Clotho Clotho] software originally presented by the [https://2008.igem.org/Team:UC_Berkeley_Tools 2008 Berkeley iGEM Software team].
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An overview of our delivery mechanism is presented below:
An overview of our delivery mechanism is presented below:

Revision as of 18:41, 26 October 2010

Overview header.png



This year our goal was to engineer Escheria Coli bacteria to serve as a vector for delivering proteins to the cytoplasms of phagocytic eukaryotes. Our project focuses on the delivery of GFP to the cytoplasm of choanoflagellates. (See Motivation for more information on choice of choanoflagellates).
We are excited to report that we have been able to achieve successful delivery of GFP to the cytoplasms of choanoflagellates with a high rate of delivery! Visit our Results page for more information. While we focused on delivery of GFP to choanoflagellates, we have built other more interesting Payloads and we are working on delivering these and GFP to other eukaryotic organisms. The design and execution of our project brought up issues of biosafety, which are discussed on our Human Practices page. In addition to the wet lab work outlined above, our team made significant improvements to the Clotho software originally presented by the 2008 Berkeley iGEM Software team.
An overview of our delivery mechanism is presented below:

Delivery Scheme

We start with a bacteria that expresses a Payload, either proteins, nucleic acids, or a combination both and a payload delivery device. We define a payload delivery device as the combination of a Self-Lysis part and a Vesicle-Buster part.
BacteriaWithPayload.jpg
Choanoflagellates naturally eat bacteria, so during normal digestion the choanoflagellate envelopes bacteria in a phagocytotic vesicle. When the bacteria is in the phagocytotic vesicle, there are two barriers between our payload and the cytoplasm of the choanoflagellate, the bacteria's own membranes, and the vesicle membrane itself. BacteriaInVesicleInChoano.jpg
This vesicle is then transported to choanoflagellate's food vacuole, where it merges with the vacuole. At this point the contents of the vesicle are exposed to the inside of the food vacuole and everything is destroyed, including the bacteria and all its contents. ChoanoDigestingBacteria.jpg
In order to achieve successful delivery, our bacteria must be able to deliver the payload in the short time between ingestion and digestion. Once our bacteria is engulfed by the choanoflagellate, and an inducer is added, it lyses itself using the Self-Lysis device derived from the 2008 UC Berkeley iGEM team. LysingBacteriaInChoano.jpg
At this point, the proteins being expressed by the bacteria will be released into the vesicle. Included in these proteins is the Vesicle-Buster device, which punctures the food vesicle membrane and releases the payload into the cytoplasm of the choanoflagellate. BustingVesicleInChoano.jpg