Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals

Kiwimagi & Letendre et al. present a workflow to quantitatively define recombinase-based digitizer and predict responses to different input signals. With a mechanistic/phenotypic model that can predict circuit performance, they generate a synthetic cell-cell communication device that amplifies a...

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Main Authors: Katherine A. Kiwimagi, Justin H. Letendre, Benjamin H. Weinberg, Junmin Wang, Mingzhe Chen, Leandro Watanabe, Chris J. Myers, Jacob Beal, Wilson W. Wong, Ron Weiss
Format: Article
Language:English
Published: Nature Portfolio 2021-07-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-021-02325-5
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author Katherine A. Kiwimagi
Justin H. Letendre
Benjamin H. Weinberg
Junmin Wang
Mingzhe Chen
Leandro Watanabe
Chris J. Myers
Jacob Beal
Wilson W. Wong
Ron Weiss
author_facet Katherine A. Kiwimagi
Justin H. Letendre
Benjamin H. Weinberg
Junmin Wang
Mingzhe Chen
Leandro Watanabe
Chris J. Myers
Jacob Beal
Wilson W. Wong
Ron Weiss
author_sort Katherine A. Kiwimagi
collection DOAJ
description Kiwimagi & Letendre et al. present a workflow to quantitatively define recombinase-based digitizer and predict responses to different input signals. With a mechanistic/phenotypic model that can predict circuit performance, they generate a synthetic cell-cell communication device that amplifies a synNotch output signal.
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spelling doaj.art-d4030bb1a2c34df186adb664ad87a9082022-12-21T23:37:10ZengNature PortfolioCommunications Biology2399-36422021-07-014111210.1038/s42003-021-02325-5Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signalsKatherine A. Kiwimagi0Justin H. Letendre1Benjamin H. Weinberg2Junmin Wang3Mingzhe Chen4Leandro Watanabe5Chris J. Myers6Jacob Beal7Wilson W. Wong8Ron Weiss9Biological Engineering, Massachusetts Institute of TechnologyDepartment of Biomedical Engineering and Biological Design Center, Boston UniversityDepartment of Biomedical Engineering and Biological Design Center, Boston UniversityThe Bioinformatics Graduate Program, Boston UniversityBiological Engineering, Massachusetts Institute of TechnologyDepartment of Electrical and Computer Engineering, University of UtahDepartment of Electrical and Computer Engineering, University of UtahRaytheon BBN TechnologiesDepartment of Biomedical Engineering and Biological Design Center, Boston UniversityBiological Engineering, Massachusetts Institute of TechnologyKiwimagi & Letendre et al. present a workflow to quantitatively define recombinase-based digitizer and predict responses to different input signals. With a mechanistic/phenotypic model that can predict circuit performance, they generate a synthetic cell-cell communication device that amplifies a synNotch output signal.https://doi.org/10.1038/s42003-021-02325-5
spellingShingle Katherine A. Kiwimagi
Justin H. Letendre
Benjamin H. Weinberg
Junmin Wang
Mingzhe Chen
Leandro Watanabe
Chris J. Myers
Jacob Beal
Wilson W. Wong
Ron Weiss
Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
Communications Biology
title Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
title_full Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
title_fullStr Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
title_full_unstemmed Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
title_short Quantitative characterization of recombinase-based digitizer circuits enables predictable amplification of biological signals
title_sort quantitative characterization of recombinase based digitizer circuits enables predictable amplification of biological signals
url https://doi.org/10.1038/s42003-021-02325-5
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