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首页> 外文期刊>PLoS Computational Biology >Chemotaxis in Escherichia coli : A Molecular Model for Robust Precise Adaptation
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Chemotaxis in Escherichia coli : A Molecular Model for Robust Precise Adaptation

机译:大肠埃希氏菌的趋化性:鲁棒精确适应的分子模型。

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The chemotaxis system in the bacterium Escherichia coli is remarkably sensitive to small relative changes in the concentrations of multiple chemical signals over a broad range of ambient concentrations. Interactions among receptors are crucial to this sensitivity as is precise adaptation, the return of chemoreceptor activity to prestimulus levels in a constant chemoeffector environment. Precise adaptation relies on methylation and demethylation of chemoreceptors by the enzymes CheR and CheB, respectively. Experiments indicate that when transiently bound to one receptor, these enzymes act on small assistance neighborhoods (AN) of five to seven receptor homodimers. In this paper, we model a strongly coupled complex of receptors including dynamic CheR and CheB acting on ANs. The model yields sensitive response and precise adaptation over several orders of magnitude of attractant concentrations and accounts for different responses to aspartate and serine. Within the model, we explore how the precision of adaptation is limited by small AN size as well as by CheR and CheB kinetics (including dwell times, saturation, and kinetic differences among modification sites) and how these kinetics contribute to noise in complex activity. The robustness of our dynamic model for precise adaptation is demonstrated by randomly varying biochemical parameters.
机译:大肠杆菌的化学趋化系统对多种化学信号的浓度在较宽的环境浓度范围内的微小相对变化非常敏感。受体之间的相互作用对于这种敏感性至关重要,因为精确的适应是在恒定的化学效应器环境中化学感受器活性恢复到刺激水平。精确的适应分别取决于化学受体CheR和CheB的甲基化和去甲基化。实验表明,当这些酶与一个受体瞬时结合时,它们作用于5至7个受体同型二聚体的小辅助区域(AN)。在本文中,我们对受体的强耦合复合物进行建模,其中包括作用于AN的动态CheR和CheB。该模型在几个数量级的引诱剂浓度上产生敏感的响应和精确的适应,并说明了对天冬氨酸和丝氨酸的不同响应。在模型中,我们探讨了自适应的精度如何受到较小的AN大小以及CheR和CheB动力学(包括停留时间,饱和度和修饰位点之间的动力学差异)的限制,以及这些动力学如何导致复杂活动中的噪声。随机变化的生化参数证明了我们用于精确适应的动态模型的鲁棒性。

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