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An allosteric model for heterogeneous receptor complexes: Understanding bacterial chemotaxis responses to multiple stimuli

机译:异构受体复合物的变构模型:了解细菌对多种刺激的趋化反应

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摘要

The classical Monod-Wyman-Changeux model for homogeneous allosteric protein complex is generalized in this article to model the responses of heterogeneous receptor complexes to multiple types of ligand stimulus. We show that the recent in vivo experimental data of Escherichia coli chemotaxis responses for mutant strains with different expression levels of the chemo-receptors to different types of stimulus [Sourjik, V. & Berg, H. C. (2004) Nature 428, 437–441] all can be explained consistently within this generalized Monod-Wyman-Changeux model. Based on the model and the existing data, responses of all of the strains (studied in this article) to the presence of any combinations of ligand (Ser and MeAsp) concentrations are predicted quantitatively for future experimental verification. Through modeling the in vivo response data, our study reveals important information about the properties of different types of individual receptors, as well as the composition of the cluster. The energetic contribution of the nonligand binding, cytoplasmic parts of the cluster, such as CheA and CheW, is also discussed. The generalized allosteric model provides a consistent framework in understanding signal integration and differentiation in bacterial chemotaxis. It should also be useful for studying the functions of other heterogeneous receptor complexes.
机译:本文推广了经典的Monod-Wyman-Changeux模型用于同构变构蛋白复合物,以建模异质受体复合物对多种类型配体刺激的响应。我们显示,最近的化学实验结果表明,大肠杆菌对不同类型的刺激具有不同的化学受体表达水平的突变株具有化学趋化反应[Sourjik,V.&Berg,HC(2004)Nature 428,437–441]。所有这些都可以在此广义Monod-Wyman-Changeux模型中得到一致解释。根据模型和现有数据,定量预测所有菌株(本文研究)对配体(Ser和MeAsp)浓度任何组合的存在的反应,以供将来进行实验验证。通过对体内反应数据进行建模,我们的研究揭示了有关不同类型的单个受体的特性以及簇的组成的重要信息。还讨论了非配体结合,簇的胞质部分(例如CheA和CheW)的能量贡献。广义的变构模型为理解细菌趋化性中的信号整合和分化提供了一个一致的框架。它对于研究其他异质受体复合物的功能也应该是有用的。

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