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Published July 20, 2022 | Published + Submitted + Supplemental Material
Journal Article Open

Localization of signaling receptors maximizes cellular information acquisition in spatially structured natural environments

Abstract

Cells in natural environments, such as tissue or soil, sense and respond to extracellular ligands with intricately structured and non-monotonic spatial distributions, sculpted by processes such as fluid flow and substrate adhesion. In this work, we show that spatial sensing and navigation can be optimized by adapting the spatial organization of signaling pathways to the spatial structure of the environment. We develop an information-theoretic framework for computing the optimal spatial organization of a sensing system for a given signaling environment. We find that receptor localization previously observed in cells maximizes information acquisition in simulated natural contexts, including tissue and soil. Specifically, information acquisition is maximized when receptors form localized patches at regions of maximal ligand concentration. Receptor localization extends naturally to produce a dynamic protocol for continuously redistributing signaling receptors, which when implemented using simple feedback, boosts cell navigation efficiency by 30-fold.

Additional Information

© 2022 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Received 5 November 2021, Revised 8 February 2022, Accepted 12 May 2022, Available online 8 June 2022. We thank Michael Elowitz, Erik Winfree, and David Sivak for scientific discussions; Dominik Schildknecht, Han Kim, Guruprasad Raghavan, Pranav Bhamidipati, Abdullah Farooq for feedback on the manuscript; Inna-Marie Strazhnik for illustrations; and Angela Anderson for editorial advice. We also would like to thank Eugenio Marco and Katarzyna Rejniak for technical advice with receptor feedback and tissue simulations, respectively. The authors would like to acknowledge the Heritage Medical Research Institute and Packard Foundation for funding and intellectual support. Author contributions: Conceptualization, Z.J.W. and M.T.; methodology, Z.J.W. and M.T.; manuscript writing, Z.J.W. and M.T.; supervision, M.T.; funding acquisition, M.T. Declaration of interests: M.T. is a member of the advisory board of Cell Systems. Data and code availability: All data have been deposited on the Caltech Research Data Repository and are publicly available as of the date of publication. DOIs are listed in the key resources table. All original code has been deposited at Zenodo (10.5281/zenodo.6432083) and is publicly available as of the date of publication. DOIs are listed in the key resources table. Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

Attached Files

Published - 1-s2.0-S2405471222002253-main.pdf

Submitted - 2021.07.01.450787v4.full.pdf

Supplemental Material - 1-s2.0-S2405471222002253-mmc1.pdf

Supplemental Material - 1-s2.0-S2405471222002253-mmc2.pdf

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Additional details

Created:
August 22, 2023
Modified:
December 22, 2023