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Biased Random Walk by Stochastic Fluctuations of Chemoattractant-Receptor Interactions at the Lower Limit of Detection

机译:在检测下限受趋化因子-受体相互作用的随机波动影响的偏向随机游动

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摘要

Binding of ligand to its receptor is a stochastic process that exhibits fluctuations in time and space. In chemotaxis, this leads to a noisy input signal. Therefore, in a gradient of chemoattractant, the cell may occasionally experience a “wrong” gradient of occupied receptors. We obtained a simple equation for Ppos, the probability that half of the cell closest to the source of chemoattractant has higher receptor occupancy than the opposite half of the cell. Ppos depends on four factors, the gradient property the receptor characteristic a time-averaging constant I, and nonreceptor noise σB. We measured chemotaxis of Dictyostelium cells to known shallow gradients of cAMP and obtained direct estimates for these constants. Furthermore, we observed that in shallow gradients, the measured chemotaxis index is correlated with Ppos, which suggests that chemotaxis in shallow gradients is a pure biased random walk. From the observed chemotaxis and derived time-averaging constant, we deduce that the gradient transducing second messenger has a lifetime of 2–8 s and a diffusion rate constant of ∼1 μm2/s. Potential candidates for such second messengers are discussed.
机译:配体与其受体的结合是随机过程,表现出时间和空间的波动。在趋化过程中,这会导致输入信号嘈杂。因此,在趋化因子的梯度中,细胞有时可能会遇到“错误”的受体占据梯度。我们获得了一个简单的Ppos方程,即最接近趋化因子来源的一半细胞比另一半细胞具有更高的受体占有率。 Ppos取决于四个因素,受体的梯度特性,时均常数I和非受体噪声σB。我们测量了Dictyostelium细胞对已知cAMP浅梯度的趋化性,并获得了这些常数的直接估计值。此外,我们观察到在浅梯度中,测得的趋化性指数与Ppos相关,这表明在浅梯度中的趋化性是纯有偏向的随机游动。从观察到的趋化性和推导的时间平均常数,我们推论出梯度转导第二信使的寿命为2-8 s,扩散速率常数约为1μm 2 / s。讨论了此类第二信使的潜在候选者。

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