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...

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Detalles Bibliográficos
Autores principales: Dana C. Nadler, Stacy-Anne Morgan, Avi Flamholz, Kaitlyn E. Kortright, David F. Savage
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/8d05fc327b244948b82af826e79987c9
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Sumario: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.