Team:Virginia

From 2011.igem.org

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'''WEBSITE UNDER CONSTRUCTION--CHECK BACK AFTER SEPTEMBER 28TH'''
'''WEBSITE UNDER CONSTRUCTION--CHECK BACK AFTER SEPTEMBER 28TH'''
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Hi! We're the iGEM team at the University of Virginia. We're engineering a genetic circuit in yeast to accelerate human wound-healing with the goal of preventing dangerous infection which is often exacerbated in chronic or slow-healing wounds. We hope to accomplish this by expressing a set of growth factors associated with accelerated healing in a time-dependent fashion by microorganisms at the wound site.
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Hi! We're the iGEM team at the University of Virginia.
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'''A Synthetic Biology Approach to Promoting Angionesis at Traumatic Wound Sites'''
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We use a synthetic biology approach to promote tissue regeneration at traumatic wound sites. Tissue regeneration is composed of three primary processes: the regrowth of functional parenchymal tissue, the regrowth of support tissues, and the regrowth of vasculature to sustain the nascent tissue formation (angiogenesis).
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Although tissue engineering has offered several effective solutions to address the first two processes, our project attempts to build upon these ideas and develop a more cost-effective and robust method to promote angiogenesis at traumatic wound sites. We have devised a circuit to be incorporated in a yeast chassis that efficiently expresses two vital angiogenic proteins--vascular endothelial growth factor (VEGF) and platelet derived growth factor (PDGF-B)--in a sequential and time-dependent manner that approximates the natural cascade of growth factor release in the human body. We also intend to submit a Biobrick-compatible yeast plasmid backbone for future use.
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Revision as of 21:36, 1 September 2011

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WEBSITE UNDER CONSTRUCTION--CHECK BACK AFTER SEPTEMBER 28TH

Hi! We're the iGEM team at the University of Virginia.

A Synthetic Biology Approach to Promoting Angionesis at Traumatic Wound Sites

We use a synthetic biology approach to promote tissue regeneration at traumatic wound sites. Tissue regeneration is composed of three primary processes: the regrowth of functional parenchymal tissue, the regrowth of support tissues, and the regrowth of vasculature to sustain the nascent tissue formation (angiogenesis). Although tissue engineering has offered several effective solutions to address the first two processes, our project attempts to build upon these ideas and develop a more cost-effective and robust method to promote angiogenesis at traumatic wound sites. We have devised a circuit to be incorporated in a yeast chassis that efficiently expresses two vital angiogenic proteins--vascular endothelial growth factor (VEGF) and platelet derived growth factor (PDGF-B)--in a sequential and time-dependent manner that approximates the natural cascade of growth factor release in the human body. We also intend to submit a Biobrick-compatible yeast plasmid backbone for future use.