Design and implementation of a synthetic biomolecular concentration tracker
Abstract
As a field, synthetic biology strives to engineer increasingly complex artificial systems in living cells. Active feedback in closed loop systems offers a dynamic and adaptive way to ensure constant relative activity independent of intrinsic and extrinsic noise. In this work, we use synthetic protein scaffolds as a modular and tunable mechanism for concentration tracking through negative feedback. Input to the circuit initiates scaffold production, leading to colocalization of a two-component system and resulting in the production of an inhibitory antiscaffold protein. Using a combination of modeling and experimental work, we show that the biomolecular concentration tracker circuit achieves dynamic protein concentration tracking in Escherichia coli and that steady state outputs can be tuned.
Additional Information
© 2014 American Chemical Society. ACS AuthorChoice - This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. Received: January 16, 2014; Published: May 6, 2014. This article is part of the Circuits in Metabolic Engineering special issue. The authors thank J. Kim for insightful discussion and suggestions on the model, and Y.E. Wang for help with Western blots. This research was conducted with government support under and awarded by DoD, Air Force Office of Scientific Research, National Defense Science and Engineering Graduate (NDSEG) Fellowship, 32 CFR 168a. Additional support was granted in part by the Benjamin M. Rosen Bioengineering Center, the NIH/NRSA Training Grant 5 T32 GM07616, the Gordon and Betty Moore Foundation through Grant GBMF2809 to the Caltech Programmable Molecular Technology Initiative, and the Institute for Collaborative Biotechnologies through Grant W911NF-09-0001 from the U.S. Army Research Office. The content of the information does not necessarily reflect the position or the policy of the Government, and no official endorsement should be inferred.Attached Files
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Supplemental Material - sb500024b_si_002.zip
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Additional details
- PMCID
- PMC4384833
- Eprint ID
- 45197
- Resolver ID
- CaltechAUTHORS:20140424-150617268
- Air Force Office of Scientific Research (AFOSR)
- National Defense Science and Engineering Graduate (NDSEG) Fellowship
- 32 CFR 168a
- Benjamin M. Rosen Bioengineering Center
- NIH Predoctoral Fellowship
- 5 T32 GM07616
- Gordon and Betty Moore Foundation
- GBMF2809
- Army Research Office (ARO)
- W911NF-09-0001
- Created
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2014-04-24Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field