Rapid construction of metabolite biosensors using domain-insertion profiling
In the construction of single fluorescent protein biosensors, selection of the insertion point of a fluorescent protein into a ligand-binding domain is a rate-limiting step. Here, the authors develop an unbiased, high-throughput approach, called domain insertion profiling with DNA sequencing (DIP-se...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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Nature Portfolio
2016-07-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/ncomms12266 |
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author | Dana C. Nadler Stacy-Anne Morgan Avi Flamholz Kaitlyn E. Kortright David F. Savage |
author_facet | Dana C. Nadler Stacy-Anne Morgan Avi Flamholz Kaitlyn E. Kortright David F. Savage |
author_sort | Dana C. Nadler |
collection | DOAJ |
description | In the construction of single fluorescent protein biosensors, selection of the insertion point of a fluorescent protein into a ligand-binding domain is a rate-limiting step. Here, the authors develop an unbiased, high-throughput approach, called domain insertion profiling with DNA sequencing (DIP-seq), to generate a novel trehalose biosensor. |
first_indexed | 2024-12-17T19:26:01Z |
format | Article |
id | doaj.art-8d05fc327b244948b82af826e79987c9 |
institution | Directory Open Access Journal |
issn | 2041-1723 |
language | English |
last_indexed | 2024-12-17T19:26:01Z |
publishDate | 2016-07-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Nature Communications |
spelling | doaj.art-8d05fc327b244948b82af826e79987c92022-12-21T21:35:23ZengNature PortfolioNature Communications2041-17232016-07-017111110.1038/ncomms12266Rapid construction of metabolite biosensors using domain-insertion profilingDana C. Nadler0Stacy-Anne Morgan1Avi Flamholz2Kaitlyn E. Kortright3David F. Savage4Department of Molecular & Cell Biology, University of CaliforniaDepartment of Molecular & Cell Biology, University of CaliforniaDepartment of Molecular & Cell Biology, University of CaliforniaDepartment of Molecular & Cell Biology, University of CaliforniaDepartment of Molecular & Cell Biology, University of CaliforniaIn the construction of single fluorescent protein biosensors, selection of the insertion point of a fluorescent protein into a ligand-binding domain is a rate-limiting step. Here, the authors develop an unbiased, high-throughput approach, called domain insertion profiling with DNA sequencing (DIP-seq), to generate a novel trehalose biosensor.https://doi.org/10.1038/ncomms12266 |
spellingShingle | Dana C. Nadler Stacy-Anne Morgan Avi Flamholz Kaitlyn E. Kortright David F. Savage Rapid construction of metabolite biosensors using domain-insertion profiling Nature Communications |
title | Rapid construction of metabolite biosensors using domain-insertion profiling |
title_full | Rapid construction of metabolite biosensors using domain-insertion profiling |
title_fullStr | Rapid construction of metabolite biosensors using domain-insertion profiling |
title_full_unstemmed | Rapid construction of metabolite biosensors using domain-insertion profiling |
title_short | Rapid construction of metabolite biosensors using domain-insertion profiling |
title_sort | rapid construction of metabolite biosensors using domain insertion profiling |
url | https://doi.org/10.1038/ncomms12266 |
work_keys_str_mv | AT danacnadler rapidconstructionofmetabolitebiosensorsusingdomaininsertionprofiling AT stacyannemorgan rapidconstructionofmetabolitebiosensorsusingdomaininsertionprofiling AT aviflamholz rapidconstructionofmetabolitebiosensorsusingdomaininsertionprofiling AT kaitlynekortright rapidconstructionofmetabolitebiosensorsusingdomaininsertionprofiling AT davidfsavage rapidconstructionofmetabolitebiosensorsusingdomaininsertionprofiling |