Abstract
To navigate their surroundings, cells rely on sensory input that is corrupted by noise. In cells performing chemotaxis, such noise arises from the stochastic binding of signalling molecules at low chemoattractant concentrations. We reveal a fundamental relationship between the speed of chemotactic steering and the strength of directional fluctuations that result from the amplification of noise in a chemical input signal. This relation implies a trade-off between steering that is slow and reliable, and steering that is fast but less reliable. We show that dynamic switching between these two modes of steering can substantially increase the probability to find a target, such as an egg to be found by sperm cells. This decision making confers no advantage in the absence of noise, but is beneficial when chemical signals are detectable, yet characterized by low signal-to-noise ratios. The latter applies at intermediate distances from a target, where signalling molecules are diluted, thus defining a ‘noise zone’ that cells have to cross. Our results explain decision making observed in recent experiments on sea urchin sperm chemotaxis. More generally, our theory demonstrates how decision making enables chemotactic agents to cope with high levels of noise in gradient sensing by dynamically adjusting the persistence length of a biased random walk.
Highlights
Motile cells successfully navigate in external concentration fields of signalling molecules by steering in the direction of local concentration gradients—a process termed chemotaxis
Efficient chemotaxis strategies must be adapted to this molecular shot noise of concentration measurements
We reveal a fundamental relationship between the speed of chemotactic steering and the strength of directional fluctuations that result from the amplification of noise
Summary
Motile cells successfully navigate in external concentration fields of signalling molecules by steering in the direction of local concentration gradients—a process termed chemotaxis. Cells must count individual binding events of signalling molecules, which represents a stochastic Poisson process Pioneering work on this topic studied the chemotaxis of mobile agents with advanced information processing skills [9], or even a capacity to compute spatial maps of maximum likelihood of target position [10]. It is an open question how biological cells with limited information processing capability deal with noise during their chemotaxis [11,12,13]
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