First-passage time to clear the way for receptor-ligand binding in a crowded environment

Abstract

Certain biological reactions, such as receptor-ligand binding at cell-cell interfaces and macromolecules binding to biopolymers, require many smaller molecules crowding a reaction site to be cleared. Examples include the T cell interface, a key player in immunological information processing. Diffusion sets a limit for such cavitation to occur spontaneously, thereby defining a timescale below which active mechanisms must take over. We consider $N$ independent diffusing particles in a closed domain, containing a sub-region with $N_0$ particles, on average. We investigate the time until the sub-region is empty, allowing a subsequent reaction to proceed. The first passage time is computed using an efficient exact simulation algorithm and an asymptotic approximation in the limit that cavitation is rare. In this limit, we find that the mean first passage time is sub-exponential, $T\propto e^{N_0}/N_0^2$. For the case of T cell receptors, we find that stochastic cavitation is exceedingly slow, $10^9$ seconds at physiological densities, however can be accelerated to occur within 5 second with only a four-fold dilution.

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Cited by in corpus (5)

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• Controlling Uncertainty of Empirical First-Passage Times in the Small-Sample Regime
• Sign-changes as a universal concept in first-passage time calculations
• Concentration of Empirical First-Passage Times
• First passage times of transport on planar spatial networks and their connections to off-network planar diffusion