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Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices

Synthetic biology aims to design de novo biological systems and reengineer existing ones. These efforts have mostly focused on transcriptional circuits, with reengineering of signaling circuits hampered by limited understanding of their systems dynamics and experimental challenges. Bacterial two-com...

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Autores principales: Amin, Munia, Kothamachu, Varun B., Feliu, Elisenda, Scharf, Birgit E., Porter, Steven L., Soyer, Orkun S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214558/
https://www.ncbi.nlm.nih.gov/pubmed/25357192
http://dx.doi.org/10.1371/journal.pcbi.1003890
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author Amin, Munia
Kothamachu, Varun B.
Feliu, Elisenda
Scharf, Birgit E.
Porter, Steven L.
Soyer, Orkun S.
author_facet Amin, Munia
Kothamachu, Varun B.
Feliu, Elisenda
Scharf, Birgit E.
Porter, Steven L.
Soyer, Orkun S.
author_sort Amin, Munia
collection PubMed
description Synthetic biology aims to design de novo biological systems and reengineer existing ones. These efforts have mostly focused on transcriptional circuits, with reengineering of signaling circuits hampered by limited understanding of their systems dynamics and experimental challenges. Bacterial two-component signaling systems offer a rich diversity of sensory systems that are built around a core phosphotransfer reaction between histidine kinases and their output response regulator proteins, and thus are a good target for reengineering through synthetic biology. Here, we explore the signal-response relationship arising from a specific motif found in two-component signaling. In this motif, a single histidine kinase (HK) phosphotransfers reversibly to two separate output response regulator (RR) proteins. We show that, under the experimentally observed parameters from bacteria and yeast, this motif not only allows rapid signal termination, whereby one of the RRs acts as a phosphate sink towards the other RR (i.e. the output RR), but also implements a sigmoidal signal-response relationship. We identify two mathematical conditions on system parameters that are necessary for sigmoidal signal-response relationships and define key parameters that control threshold levels and sensitivity of the signal-response curve. We confirm these findings experimentally, by in vitro reconstitution of the one HK-two RR motif found in the Sinorhizobium meliloti chemotaxis pathway and measuring the resulting signal-response curve. We find that the level of sigmoidality in this system can be experimentally controlled by the presence of the sink RR, and also through an auxiliary protein that is shown to bind to the HK (yielding Hill coefficients of above 7). These findings show that the one HK-two RR motif allows bacteria and yeast to implement tunable switch-like signal processing and provides an ideal basis for developing threshold devices for synthetic biology applications.
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spelling pubmed-42145582014-11-05 Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices Amin, Munia Kothamachu, Varun B. Feliu, Elisenda Scharf, Birgit E. Porter, Steven L. Soyer, Orkun S. PLoS Comput Biol Research Article Synthetic biology aims to design de novo biological systems and reengineer existing ones. These efforts have mostly focused on transcriptional circuits, with reengineering of signaling circuits hampered by limited understanding of their systems dynamics and experimental challenges. Bacterial two-component signaling systems offer a rich diversity of sensory systems that are built around a core phosphotransfer reaction between histidine kinases and their output response regulator proteins, and thus are a good target for reengineering through synthetic biology. Here, we explore the signal-response relationship arising from a specific motif found in two-component signaling. In this motif, a single histidine kinase (HK) phosphotransfers reversibly to two separate output response regulator (RR) proteins. We show that, under the experimentally observed parameters from bacteria and yeast, this motif not only allows rapid signal termination, whereby one of the RRs acts as a phosphate sink towards the other RR (i.e. the output RR), but also implements a sigmoidal signal-response relationship. We identify two mathematical conditions on system parameters that are necessary for sigmoidal signal-response relationships and define key parameters that control threshold levels and sensitivity of the signal-response curve. We confirm these findings experimentally, by in vitro reconstitution of the one HK-two RR motif found in the Sinorhizobium meliloti chemotaxis pathway and measuring the resulting signal-response curve. We find that the level of sigmoidality in this system can be experimentally controlled by the presence of the sink RR, and also through an auxiliary protein that is shown to bind to the HK (yielding Hill coefficients of above 7). These findings show that the one HK-two RR motif allows bacteria and yeast to implement tunable switch-like signal processing and provides an ideal basis for developing threshold devices for synthetic biology applications. Public Library of Science 2014-10-30 /pmc/articles/PMC4214558/ /pubmed/25357192 http://dx.doi.org/10.1371/journal.pcbi.1003890 Text en © 2014 Amin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Amin, Munia
Kothamachu, Varun B.
Feliu, Elisenda
Scharf, Birgit E.
Porter, Steven L.
Soyer, Orkun S.
Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title_full Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title_fullStr Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title_full_unstemmed Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title_short Phosphate Sink Containing Two-Component Signaling Systems as Tunable Threshold Devices
title_sort phosphate sink containing two-component signaling systems as tunable threshold devices
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214558/
https://www.ncbi.nlm.nih.gov/pubmed/25357192
http://dx.doi.org/10.1371/journal.pcbi.1003890
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