Microscale velocity-dependent unbinding generates a macroscale performance-efficiency tradeoff in actomyosin systems
Jake McGrath, Brian Kent, Colin Johnson, Jos\'e Alvarado

TL;DR
This paper develops an analytical model linking microscale myosin unbinding dynamics to macroscale muscle performance and efficiency, validated by robotic experiments and muscle data, revealing a fundamental tradeoff governed by a key parameter.
Contribution
It introduces a novel analytical model connecting microscale unbinding parameter to macroscale energetics and demonstrates this with a robophysical model and biological data.
Findings
Uncovered a performance-efficiency tradeoff governed by the unbinding parameter α.
Validated the model with in-vivo muscle data and robotic experiments.
Identified a typical α value in muscle and myoblasts indicating a balance between power and efficiency.
Abstract
Myosin motors are fundamental biological actuators, powering diverse mechanical tasks in eukaryotic cells via ATP hydrolysis. Recent work revealed that myosin's velocity-dependent detachment rate can bridge actomyosin dynamics to macroscale Hill muscle predictions. However, the influence of this microscale unbinding, which we characterize by a dimensionless parameter , on macroscale energetic flows-such as power consumption, output and efficiency-remains elusive. Here we develop an analytical model of myosin dynamics that relates unbinding rates to energetics. Our model agrees with published in-vivo muscle data and, furthermore, uncovers a performance-efficiency tradeoff governed by . To experimentally validate the tradeoff, we build HillBot, a robophysical model of Hill's muscle that mimics nonlinearity. Through HillBot, we decouple 's concurrent effect…
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Taxonomy
TopicsNeuroscience and Neural Engineering · Force Microscopy Techniques and Applications
