Surface Displayed SNAP as a New Reporter  in Synthetic Biology

The field of synthetic biology has leveraged engineering tools such as molecular cloning to create new biological components, networks, and processes. While many of these components and networks have been deployed in the cytosol, there is a shortage of systems that utilize the surface of the cell. I...

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Main Author: Scott, Felicia Yi Xia
Other Authors: Biological Systems Engineering
Format: Others
Published: Virginia Tech 2017
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Online Access:http://hdl.handle.net/10919/73915
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spelling ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-739152020-11-19T05:46:27Z Surface Displayed SNAP as a New Reporter  in Synthetic Biology Scott, Felicia Yi Xia Biological Systems Engineering Ruder, Warren Christopher Barone, Justin R. Cheng, Chao-Min Synthetic Biology Genetic Reporter Surface Display Proteins The field of synthetic biology has leveraged engineering tools such as molecular cloning to create new biological components, networks, and processes. While many of these components and networks have been deployed in the cytosol, there is a shortage of systems that utilize the surface of the cell. In order to address this shortcoming, we have created a synthetic, surface-displayed substrate anchor for bacteria. This approach allows us to engineer surface-based synthetic biological systems as a complement to existing intracellular approaches. We leveraged the tools of synthetic biology to display a catalytically active enzyme that covalently bonds itself to benzylguanine (BG) groups. We created a fusion protein allowing us to place human O6-alkylguanine DNA alkyltransferase (hAGT), also known as SNAP, on the surface of a bacterial cell. Initially, we used this synthetic component as a tool for spatially segregating orthogonal synthetic gene outputs by visualizing an extracellular synthetic green fluorescent reporter, SNAP-Cell® 505-Star, simultaneously with an intracellular red fluorescent protein, mCherry. Moreover, we have shown that our construct enables cells to selectively bond to BG-conjugated magnetic beads. As a result, we have demonstrated that surface displayed SNAP facilitates engineering a direct channel between intracellular gene expression and extracellular material capture. In the near future, we believe this magnetic capture can be expanded as a sortable reporter for synthetic biology as a direct extension of this work. Moreover, our work serves as an enabling technology, paving the way for extracellular synthetic biological systems that may coexist orthogonally to intracellular processes. Master of Science 2017-01-01T07:00:21Z 2017-01-01T07:00:21Z 2015-07-10 Thesis vt_gsexam:5267 http://hdl.handle.net/10919/73915 In Copyright http://rightsstatements.org/vocab/InC/1.0/ ETD application/pdf Virginia Tech
collection NDLTD
format Others
sources NDLTD
topic Synthetic Biology
Genetic Reporter
Surface Display Proteins
spellingShingle Synthetic Biology
Genetic Reporter
Surface Display Proteins
Scott, Felicia Yi Xia
Surface Displayed SNAP as a New Reporter  in Synthetic Biology
description The field of synthetic biology has leveraged engineering tools such as molecular cloning to create new biological components, networks, and processes. While many of these components and networks have been deployed in the cytosol, there is a shortage of systems that utilize the surface of the cell. In order to address this shortcoming, we have created a synthetic, surface-displayed substrate anchor for bacteria. This approach allows us to engineer surface-based synthetic biological systems as a complement to existing intracellular approaches. We leveraged the tools of synthetic biology to display a catalytically active enzyme that covalently bonds itself to benzylguanine (BG) groups. We created a fusion protein allowing us to place human O6-alkylguanine DNA alkyltransferase (hAGT), also known as SNAP, on the surface of a bacterial cell. Initially, we used this synthetic component as a tool for spatially segregating orthogonal synthetic gene outputs by visualizing an extracellular synthetic green fluorescent reporter, SNAP-Cell® 505-Star, simultaneously with an intracellular red fluorescent protein, mCherry. Moreover, we have shown that our construct enables cells to selectively bond to BG-conjugated magnetic beads. As a result, we have demonstrated that surface displayed SNAP facilitates engineering a direct channel between intracellular gene expression and extracellular material capture. In the near future, we believe this magnetic capture can be expanded as a sortable reporter for synthetic biology as a direct extension of this work. Moreover, our work serves as an enabling technology, paving the way for extracellular synthetic biological systems that may coexist orthogonally to intracellular processes. === Master of Science
author2 Biological Systems Engineering
author_facet Biological Systems Engineering
Scott, Felicia Yi Xia
author Scott, Felicia Yi Xia
author_sort Scott, Felicia Yi Xia
title Surface Displayed SNAP as a New Reporter  in Synthetic Biology
title_short Surface Displayed SNAP as a New Reporter  in Synthetic Biology
title_full Surface Displayed SNAP as a New Reporter  in Synthetic Biology
title_fullStr Surface Displayed SNAP as a New Reporter  in Synthetic Biology
title_full_unstemmed Surface Displayed SNAP as a New Reporter  in Synthetic Biology
title_sort surface displayed snap as a new reporter  in synthetic biology
publisher Virginia Tech
publishDate 2017
url http://hdl.handle.net/10919/73915
work_keys_str_mv AT scottfeliciayixia surfacedisplayedsnapasanewreporterinsyntheticbiology
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