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利用协同进化景观将细菌信号蛋白的序列空间与表型联系起来。

Connecting the Sequence-Space of Bacterial Signaling Proteins to Phenotypes Using Coevolutionary Landscapes.

作者信息

Cheng R R, Nordesjö O, Hayes R L, Levine H, Flores S C, Onuchic J N, Morcos F

机构信息

Center for Theoretical Biological Physics, Rice University, Houston, TX

Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.

出版信息

Mol Biol Evol. 2016 Dec;33(12):3054-3064. doi: 10.1093/molbev/msw188. Epub 2016 Sep 7.

Abstract

Two-component signaling (TCS) is the primary means by which bacteria sense and respond to the environment. TCS involves two partner proteins working in tandem, which interact to perform cellular functions whereas limiting interactions with non-partners (i.e., cross-talk). We construct a Potts model for TCS that can quantitatively predict how mutating amino acid identities affect the interaction between TCS partners and non-partners. The parameters of this model are inferred directly from protein sequence data. This approach drastically reduces the computational complexity of exploring the sequence-space of TCS proteins. As a stringent test, we compare its predictions to a recent comprehensive mutational study, which characterized the functionality of 20 mutational variants of the PhoQ kinase in Escherichia coli We find that our best predictions accurately reproduce the amino acid combinations found in experiment, which enable functional signaling with its partner PhoP. These predictions demonstrate the evolutionary pressure to preserve the interaction between TCS partners as well as prevent unwanted cross-talk. Further, we calculate the mutational change in the binding affinity between PhoQ and PhoP, providing an estimate to the amount of destabilization needed to disrupt TCS.

摘要

双组分信号传导(TCS)是细菌感知和响应环境的主要方式。TCS涉及两个协同工作的伙伴蛋白,它们相互作用以执行细胞功能,同时限制与非伙伴蛋白的相互作用(即串扰)。我们构建了一个用于TCS的Potts模型,该模型可以定量预测氨基酸身份的突变如何影响TCS伙伴蛋白与非伙伴蛋白之间的相互作用。该模型的参数直接从蛋白质序列数据中推断得出。这种方法极大地降低了探索TCS蛋白序列空间的计算复杂性。作为一项严格的测试,我们将其预测结果与最近一项全面的突变研究进行了比较,该研究对大肠杆菌中PhoQ激酶的20种突变变体的功能进行了表征。我们发现,我们的最佳预测准确地再现了实验中发现的氨基酸组合,这些组合能够与其伙伴蛋白PhoP进行功能性信号传导。这些预测证明了保留TCS伙伴蛋白之间的相互作用以及防止不必要串扰的进化压力。此外,我们计算了PhoQ和PhoP之间结合亲和力的突变变化,为破坏TCS所需的不稳定程度提供了一个估计值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8af/5100047/089daf03f081/msw188f1p.jpg

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