Foley Samuel L, Johnson Margaret E
T. C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, Maryland, USA.
ArXiv. 2025 May 22:arXiv:2505.17290v1.
Cellular decision-making based on information received from the external environment is frequently initiated by transmembrane receptors. These receptors are known to propagate such information by triggering a series of irreversible, energy-consuming reactions. While this active mechanism ensures switch-like responses, here we show how spontaneous molecular self-assembly on a two-dimensional substrate can similarly act as a tunable and robust switch for detecting receptors at physiological concentrations. This mechanism is much more sensitive than other passive mechanisms for receptor detection. We derive analytical expressions for critical receptor densities that switch on nucleation and growth of assemblies, in close agreement with equilibrium stochastic reaction-diffusion simulations. The theory developed provides testable predictions for how each component controls decision thresholds and magnitude of response.
基于从外部环境接收的信息进行的细胞决策通常由跨膜受体启动。已知这些受体通过触发一系列不可逆的、耗能的反应来传播此类信息。虽然这种主动机制确保了类似开关的响应,但在此我们展示了二维底物上的自发分子自组装如何同样能作为一种可调节且稳健的开关,用于检测生理浓度下的受体。这种机制比其他用于受体检测的被动机制要灵敏得多。我们推导了用于开启组装成核和生长的临界受体密度的解析表达式,与平衡随机反应扩散模拟结果高度吻合。所发展的理论为每个组件如何控制决策阈值和响应幅度提供了可验证的预测。