Difference between revisions of "Team:Technion Israel/Project/Overview"
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header{background-image: url("https://static.igem.org/mediawiki/2015/f/fc/Technion_Israel_2015_heading_Project_overview.jpg"); background-size: 100%; background-repeat: no-repeat; width: 100%; height: 450px; margin-bottom: 0px;} | header{background-image: url("https://static.igem.org/mediawiki/2015/f/fc/Technion_Israel_2015_heading_Project_overview.jpg"); background-size: 100%; background-repeat: no-repeat; width: 100%; height: 450px; margin-bottom: 0px;} | ||
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<h2>Solution</h2> | <h2>Solution</h2> | ||
<p>The proposed solution is to incorporate the gene of a DHT-inactivating enzyme into a bacterium that is naturally found on our scalp (<i>B.subtillis</i>). These transgenic microorganisms will be applied on the patient's scalp, and will secrete the enzyme to their environment, providing a constantly renewed supply of the treatment. The proposed DHT-inactivating enzyme is the 3α-hydroxysteroid dehydrogenase (3α-HSD) enzyme. DHT is inactivated by the 3α-HSD to form 3α-androstanediol <sup><a href="#fn13" id="ref1">13</a></sup>, as shown in figure 1 below.</p> | <p>The proposed solution is to incorporate the gene of a DHT-inactivating enzyme into a bacterium that is naturally found on our scalp (<i>B.subtillis</i>). These transgenic microorganisms will be applied on the patient's scalp, and will secrete the enzyme to their environment, providing a constantly renewed supply of the treatment. The proposed DHT-inactivating enzyme is the 3α-hydroxysteroid dehydrogenase (3α-HSD) enzyme. DHT is inactivated by the 3α-HSD to form 3α-androstanediol <sup><a href="#fn13" id="ref1">13</a></sup>, as shown in figure 1 below.</p> | ||
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+ | <figure><img class="img_center" src="https://static.igem.org/mediawiki/2015/e/e1/Technion_Israel_2015_overview-figure1.jpg"/><figcaption>Figure 1:Androgen Metabolism in the human prostate<sup><a href="#fn13" id="ref1">13</a></sup></figcaption></figure> | ||
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<p>3α-HSD exists naturally in human prostate, performing the mentioned reaction<sup><a href="#fn14" id="ref1">14</a></sup>. However, according to previous research, the isoform originated from rat liver has greater specificity to DHT than the human isoform <sup><a href="#fn14" id="ref1">14</a></sup>. Therefore, we chose to use the sequence of AKR1C9 for our project. We altered the sequence in order to delete forbidden restriction sites according to the iGEM regulations for BioBricks.</p> | <p>3α-HSD exists naturally in human prostate, performing the mentioned reaction<sup><a href="#fn14" id="ref1">14</a></sup>. However, according to previous research, the isoform originated from rat liver has greater specificity to DHT than the human isoform <sup><a href="#fn14" id="ref1">14</a></sup>. Therefore, we chose to use the sequence of AKR1C9 for our project. We altered the sequence in order to delete forbidden restriction sites according to the iGEM regulations for BioBricks.</p> | ||
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+ | <h2>The components of the project</h2> | ||
+ | <p>In order to better focus on the many different components of our project, we split up into groups to tackle each component: Expression of the 3α-HSD enzyme, secretion of the enzyme, and cofactor production. Additionally, a group worked on developing a comb- a tool which could provide a user-friendly solution for the consumer in applying our product to the scalp. For more information about each sub-group, enter the page from the menu above, or visit the links below:</br> | ||
+ | <ul style="list-style: none"><li><a href="https://2015.igem.org/Team:Technion_Israel/Project/Secretion" target="_blank">Secretion</a></li> | ||
+ | <li><a href="https://2015.igem.org/Team:Technion_Israel/Project/Secretion" target="_blank">Expression</a></li> | ||
+ | <li><a href="https://2015.igem.org/Team:Technion_Israel/Project/Cofactor" target="_blank">Cofactor</a></li> | ||
+ | <li><a href="https://2015.igem.org/Team:Technion_Israel/Design" target="_blank">Comb and Design</a></li> | ||
+ | <li><a href="https://2015.igem.org/Team:Technion_Israel/Project/Results" target="_blank">Results</a></li></p> | ||
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+ | <h2>What’s next?</h2> | ||
+ | <p>Our plans in the future consist of examining our product on model mice for androgenic alopecia (male pattern baldness) as a proof of concept. We would like to utilize this model to prove that our combined solution for this condition can actually show results (<i>in-vivo</i>). If this succeeds, we will continue on to perform human trials.</p> | ||
+ | <p>We strive to open a standalone startup which will take our concepts forward.</p> | ||
+ | <p>We also believe that our new application of utilizing the human microbiome (genetically modify it for a specific cause ) is a promising new way to treat different conditions.</p> | ||
<hr></hr> | <hr></hr> | ||
<sup id="fn1">1. "Hair Loss Statistics." Statistic Brain. Relevant Research, Inc. (International Society of Hair Restoration Surgery), July 27th 2015. (accessed on: July 7th 2015). <http://www.statisticbrain.com/hair-loss-statistics/>.</sup></br> | <sup id="fn1">1. "Hair Loss Statistics." Statistic Brain. Relevant Research, Inc. (International Society of Hair Restoration Surgery), July 27th 2015. (accessed on: July 7th 2015). <http://www.statisticbrain.com/hair-loss-statistics/>.</sup></br> | ||
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<sup id="fn13">13. Human 3-alpha hydroxysteroid dehydrogenase type 3 (3α-HSD3): The V54L mutation restricting the steroid alternative binding and enhancing the 20α-HSD activity. The Journal of Steroid Biochemistry and Molecular Biology 141, 135-143. | <sup id="fn13">13. Human 3-alpha hydroxysteroid dehydrogenase type 3 (3α-HSD3): The V54L mutation restricting the steroid alternative binding and enhancing the 20α-HSD activity. The Journal of Steroid Biochemistry and Molecular Biology 141, 135-143. | ||
</sup></br> | </sup></br> | ||
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<sup id="fn14">14. Biswas, M. G.; Russell, D.W.:Expression Cloning and Characterization of Oxidative 17b- and 3a-Hydroxysteroid Dehydrogenases from Rat and Human Prostate. The Journal of Biological Chemistry. 1997, 272, 15959-15966. | <sup id="fn14">14. Biswas, M. G.; Russell, D.W.:Expression Cloning and Characterization of Oxidative 17b- and 3a-Hydroxysteroid Dehydrogenases from Rat and Human Prostate. The Journal of Biological Chemistry. 1997, 272, 15959-15966. | ||
</sup></br> | </sup></br> |
Revision as of 21:36, 17 September 2015