Combinatorial Control through Allostery
- Creators
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Galstyan, Vahe
- Funk, Luke
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Einav, Tal
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Phillips, Rob
Abstract
Many instances of cellular signaling and transcriptional regulation involve switch-like molecular responses to the presence or absence of input ligands. To understand how these responses come about and how they can be harnessed, we develop a statistical mechanical model to characterize the types of Boolean logic that can arise from allosteric molecules following the Monod–Wyman–Changeux (MWC) model. Building upon previous work, we show how an allosteric molecule regulated by two inputs can elicit AND, OR, NAND, and NOR responses but is unable to realize XOR or XNOR gates. Next, we demonstrate the ability of an MWC molecule to perform ratiometric sensing—a response behavior where activity depends monotonically on the ratio of ligand concentrations. We then extend our analysis to more general schemes of combinatorial control involving either additional binding sites for the two ligands or an additional third ligand and show how these additions can cause a switch in the logic behavior of the molecule. Overall, our results demonstrate the wide variety of control schemes that biological systems can implement using simple mechanisms.
Additional Information
© 2019 American Chemical Society. Received: December 28, 2018; Revised: February 5, 2019; Published: February 15, 2019. It is a great pleasure to acknowledge the contributions of Bill Eaton to our understanding of allostery. We thank Chandana Gopalakrishnappa and Parijat Sil for their input on this work, and Michael Elowitz for his insights and valuable feedback on the manuscript. This research was supported by La Fondation Pierre-Gilles de Gennes, the Rosen Center at Caltech, the Department of Defense through the National Defense Science & Engineering Graduate Fellowship (NDSEG) Program (LF), and the National Institutes of Health DP1 OD000217 (Director's Pioneer Award), R01 GM085286, and 1R35 GM118043-01 (MIRA). We are grateful to the Burroughs Wellcome Fund for its support of the Physical Biology of the Cell Course at the Marine Biological Laboratory, where part of this work was completed. Author Contributions: V.G. and L.F. contributed equally to this work. The authors declare no competing financial interest.Attached Files
Accepted Version - nihms-1015047.pdf
Submitted - 1812.11290.pdf
Submitted - 508226.full.pdf
Supplemental Material - jp8b12517_si_001.zip
Supplemental Material - jp8b12517_si_002.pdf
Supplemental Material - jp8b12517_si_003.zip
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Additional details
- PMCID
- PMC6467274
- Eprint ID
- 91986
- Resolver ID
- CaltechAUTHORS:20190102-135256302
- La Fondation Pierre-Gilles de Gennes
- Donna and Benjamin M. Rosen Bioengineering Center
- National Defense Science and Engineering Graduate (NDSEG) Fellowship
- NIH
- DP1 OD000217
- NIH
- R01 GM085286
- NIH
- 1R35 GM118043-01
- Burroughs-Wellcome Fund
- Created
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2019-01-03Created from EPrint's datestamp field
- Updated
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2022-03-01Created from EPrint's last_modified field
- Caltech groups
- Rosen Bioengineering Center