Prediction and Dissipation in Nonequilibrium Molecular Sensors: Conditionally Markovian Channels Driven by Memoryful Environments

Biological sensors must often predict their input while operating under metabolic constraints. However, determining whether or not a particular sensor is evolved or designed to be accurate and efficient is challenging. This arises partly from the functional constraints being at cross purposes and pa...

Full description

Saved in:
Bibliographic Details
Published inBulletin of mathematical biology Vol. 82; no. 2; p. 25
Main Authors Marzen, Sarah E., Crutchfield, James P.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.02.2020
Springer Nature B.V
Subjects
Online AccessGet full text
ISSN0092-8240
1522-9602
1522-9602
DOI10.1007/s11538-020-00694-2

Cover

More Information
Summary:Biological sensors must often predict their input while operating under metabolic constraints. However, determining whether or not a particular sensor is evolved or designed to be accurate and efficient is challenging. This arises partly from the functional constraints being at cross purposes and partly since quantifying the prediction performance of even in silico sensors can require prohibitively long simulations, especially when highly complex environments drive sensors out of equilibrium. To circumvent these difficulties, we develop new expressions for the prediction accuracy and thermodynamic costs of the broad class of conditionally Markovian sensors subject to complex, correlated (unifilar hidden semi-Markov) environmental inputs in nonequilibrium steady state. Predictive metrics include the instantaneous memory and the total predictable information (the mutual information between present sensor state and input future), while dissipation metrics include power extracted from the environment and the nonpredictive information rate. Success in deriving these formulae relies on identifying the environment’s causal states, the input’s minimal sufficient statistics for prediction. Using these formulae, we study large random channels and the simplest nontrivial biological sensor model—that of a Hill molecule, characterized by the number of ligands that bind simultaneously—the sensor’s cooperativity. We find that the seemingly impoverished Hill molecule can capture an order of magnitude more predictable information than large random channels.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0092-8240
1522-9602
1522-9602
DOI:10.1007/s11538-020-00694-2