Team:Heidelberg

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= Project Abstract =
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'' miRNAs were found to be key regulators in proliferation, differentiation, apoptosis, hematopoesis and oncogenesis. Different cell types have unique and dynamic miRNA expression profiles that could be used to discriminate between those cell types and even between cellular stages. The iGEM Team Heidelberg 2010 will create miRNA binding site patterns enabling the control of any target gene of choice according to the cellular miRNA expression profile.  Therefore, we will apply evolutionary methods for creating large miRNA binding site pattern libraries and we will develop two new and powerful methods for miRNA binding site pattern library screening. In parallel, computational modeling will be used for getting information on natural binding site pattern structure in order to enable rational design of complex binding site patterns recognizing certain cellular miRNA expression profiles in the future.''
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The contents and design of this wiki are published under the GNU Free Documentation License. You are granted the right to copy and modify our work, but you must publish your work under the same type of license while recognizing us the authors.
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Stefan Kleinsorg, Thomas Uhlig
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{{:Team:Heidelberg/Pagetop|home}}
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<div id="wrapperheadline">iGEM Heidelberg Mission 2010: miBricks</div><br>
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<img src="https://static.igem.org/mediawiki/2010/5/5a/Febit_logo.jpg" width="150" height="100" />
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<div id="projectabstract">The great potential of gene therapy is currently limited by two major challenges:  tissue specific gene delivery and regulation of gene expression, either dependent on cell-specific properties or intentionally independent of the cellular context. We followed two synergistic tracks to address these problems.<br>
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One, we have developed a novel method for miRNA based gene expression tuning in mammalian cells, allowing the fine-tuning of gene expression based on synthetic miRNAs, as well as the cell specific on- and off-targeting based on endogenous miRNAs. We show that this method is functional in vivo and in vitro and prove the high potential of all three miRNA-based regulation approaches.<br>
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Two, we have developed a standardized and fast approach towards the creation of AAV-based gene delivery vectors. We have achieved exceptionally selective tissue-specific targeting <i>in vitro</i> and <i>in vivo</i> with hepatocyte specific delivery vectors.<br>
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We are happy to provide the synthetic biology community with two high impact innovations which will fuel the improvement of tissue specific gene therapy approaches and other medical applications of synthetic biology.</div><br><br>
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<div id="slider">
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<a href="https://2010.igem.org/Team:Heidelberg/Project/Capsid_Shuffling"><img src="https://static.igem.org/mediawiki/2010/e/ed/Slide_CapShuffling.png" alt="" rel="https://static.igem.org/mediawiki/2010/3/30/Slide_CapShuffling_thumb.png"/></a>
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<a class="piclinks" href="javascript:writeText('And we are not talking about fashion! In our team, a group of students was in charge of the computational interpretation and modeling of the data generated. Want to read more? Click <a href=&quot;https://2010.igem.org/Team:Heidelberg/Modeling&quot;>here</a>!')" onMouseOver="mouseOver(1)"  onMouseOut="mouseOut(1)" onMouseDown="mouseDown(1)" onMouseUp="mouseUp(1)">
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<a class="piclinks" href="javascript:writeText('Our team comprised a group of twenty motivated students from eight different countries, two instructors and eight advisors. Want to meet them? Click <a href=&quot;https://2010.igem.org/Team:Heidelberg/Team&quot;>here</a>!')" onMouseOver="mouseOver(2)" onMouseOut="mouseOut(2)" onMouseDown="mouseDown(2)" onMouseUp="mouseUp(2)">
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<center><table id="desc-table"><tr><td><div id ="desc" border=0><center>Please click a Button to get more information! </center></div></td></tr></table></center>
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<a class="piclinks" href="javascript:writeText('As in any piece of research, we have been keeping detailed notebooks with the experiments we have done. Want to retrace our steps? Click <a href=&quot;https://2010.igem.org/Team:Heidelberg/Notebook&quot;>here</a>!')" onMouseOver="mouseOver(4)" onMouseOut="mouseOut(4)" onMouseDown="mouseDown(4)" onMouseUp="mouseUp(4)">
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<a class="piclinks" href="javascript:writeText('We have generated more than 100 parts that have been sent to iGEM headquarters. Want to know which ones? Click <a href=&quot;https://2010.igem.org/Team:Heidelberg/Parts&quot;>here</a>!')" onMouseOver="mouseOver(5)" onMouseOut="mouseOut(5)" onMouseDown="mouseDown(5)" onMouseUp="mouseUp(5)">
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</a>
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<a class="piclinks" href="javascript:writeText('Our team was sponsored by a non-profit organization, nine companies and three academic sponsors. Want to meet them? Click <a href=&quot;https://2010.igem.org/Team:Heidelberg/Support&quot;>here</a>!')" onMouseOver="mouseOver(6)" onMouseOut="mouseOut(6)" onMouseDown="mouseDown(6)" onMouseUp="mouseUp(6)">
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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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''Tell us more about your project. Give us background. Use this as the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
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|align="center"|[[Team:Heidelberg | Team Example]]
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<!--- The Mission, Experiments --->
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<h3>The iGEM idea</h3>
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iGEM (international Genetically Engineered Machines Competition) is an international competition in synthetic biology, hosted by the MIT in Boston. The aim of this competition is to answer a basic question once posted by the director of iGEM, Randy Rettberg, as follows: "Can simple biological systems be built from standard, interchangeable parts and operated in living cells? Or is biology just too complicated to be engineered in this way?"
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<br>
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International student teams participating in the iGEM compete to answer this fundamental question by engineering biological systems with a proper function. More than 100 interdisciplinary student teams from all over the world, mainly consisting of undergraduate students in biology, biochemistry, engineering, informatics and mathematics, carry out different projects during the Summer to follow this approach.
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<br>
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Projects involved in iGEM reach from medical applications, such as genetically modified bacteria used in cancer-treatment to environmental and manufacturing projects, which allow the construction of a dynamic, watch-like counter consisting of living cells. In contrast to classical genetic engineering where only one gene is transferred from organism A to organism B, synthetic biology advances into the construction of new systems as a whole with totally new emerging properties. Therefore, each iGEM-Teams gets access to a gene-Database called "registry", where hundreds of different genetic parts with characterized functions are available in a “plug-and-play”–like manner. These parts can be simply stuck together to create new functional systems. The rising number of iGEM-Teams over the last years as well as the upcoming public interest in iGEM as well as in the iGEM-Teams’ projects and synthetic biology in general shows that synthetic biology will demonstrate an essential contribution to understand the functional way of life and have an enormous impact on many different fields of both scientific reseach and every-day life.
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{{:Team:Heidelberg/Bottom}}
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!align="center"|[[Team:Heidelberg|Home]]
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!align="center"|[[Team:Heidelberg/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=Heidelberg Official Team Profile]
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!align="center"|[[Team:Heidelberg/Project|Project]]
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!align="center"|[[Team:Heidelberg/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Heidelberg/Modeling|Modeling]]
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!align="center"|[[Team:Heidelberg/Notebook|Notebook]]
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!align="center"|[[Team:Heidelberg/Safety|Safety]]
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Latest revision as of 00:21, 18 November 2010

iGEM Heidelberg Mission 2010: miBricks

The great potential of gene therapy is currently limited by two major challenges: tissue specific gene delivery and regulation of gene expression, either dependent on cell-specific properties or intentionally independent of the cellular context. We followed two synergistic tracks to address these problems.
One, we have developed a novel method for miRNA based gene expression tuning in mammalian cells, allowing the fine-tuning of gene expression based on synthetic miRNAs, as well as the cell specific on- and off-targeting based on endogenous miRNAs. We show that this method is functional in vivo and in vitro and prove the high potential of all three miRNA-based regulation approaches.
Two, we have developed a standardized and fast approach towards the creation of AAV-based gene delivery vectors. We have achieved exceptionally selective tissue-specific targeting in vitro and in vivo with hepatocyte specific delivery vectors.
We are happy to provide the synthetic biology community with two high impact innovations which will fuel the improvement of tissue specific gene therapy approaches and other medical applications of synthetic biology.








Please click a Button to get more information!



The iGEM idea

iGEM (international Genetically Engineered Machines Competition) is an international competition in synthetic biology, hosted by the MIT in Boston. The aim of this competition is to answer a basic question once posted by the director of iGEM, Randy Rettberg, as follows: "Can simple biological systems be built from standard, interchangeable parts and operated in living cells? Or is biology just too complicated to be engineered in this way?"
International student teams participating in the iGEM compete to answer this fundamental question by engineering biological systems with a proper function. More than 100 interdisciplinary student teams from all over the world, mainly consisting of undergraduate students in biology, biochemistry, engineering, informatics and mathematics, carry out different projects during the Summer to follow this approach.
Projects involved in iGEM reach from medical applications, such as genetically modified bacteria used in cancer-treatment to environmental and manufacturing projects, which allow the construction of a dynamic, watch-like counter consisting of living cells. In contrast to classical genetic engineering where only one gene is transferred from organism A to organism B, synthetic biology advances into the construction of new systems as a whole with totally new emerging properties. Therefore, each iGEM-Teams gets access to a gene-Database called "registry", where hundreds of different genetic parts with characterized functions are available in a “plug-and-play”–like manner. These parts can be simply stuck together to create new functional systems. The rising number of iGEM-Teams over the last years as well as the upcoming public interest in iGEM as well as in the iGEM-Teams’ projects and synthetic biology in general shows that synthetic biology will demonstrate an essential contribution to understand the functional way of life and have an enormous impact on many different fields of both scientific reseach and every-day life.

Retrieved from "http://2010.igem.org/Team:Heidelberg"