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本文引用的文献

1
Stochastic assembly of chemoreceptor clusters in Escherichia coli.大肠杆菌中化学感受器簇的随机组装。
Mol Microbiol. 2008 Jun;68(5):1228-36. doi: 10.1111/j.1365-2958.2008.06227.x.
2
Protein exchange dynamics at chemoreceptor clusters in Escherichia coli.大肠杆菌中化学感受器簇处的蛋白质交换动力学
Proc Natl Acad Sci U S A. 2008 Apr 29;105(17):6403-8. doi: 10.1073/pnas.0710611105. Epub 2008 Apr 21.
3
Lipid localization in bacterial cells through curvature-mediated microphase separation.通过曲率介导的微相分离实现脂质在细菌细胞中的定位。
Biophys J. 2008 Aug;95(3):1034-49. doi: 10.1529/biophysj.107.126920. Epub 2008 Apr 4.
4
Location and architecture of the Caulobacter crescentus chemoreceptor array.新月柄杆菌化学感受器阵列的位置与结构
Mol Microbiol. 2008 Jul;69(1):30-41. doi: 10.1111/j.1365-2958.2008.06219.x. Epub 2008 Mar 19.
5
Elastic modeling of biomembranes and lipid bilayers.生物膜和脂质双层的弹性建模。
Annu Rev Phys Chem. 2008;59:685-712. doi: 10.1146/annurev.physchem.59.032607.093550.
6
Chemotaxis receptor complexes: from signaling to assembly.趋化性受体复合物:从信号传导到组装
PLoS Comput Biol. 2007 Jul;3(7):e150. doi: 10.1371/journal.pcbi.0030150. Epub 2007 Jun 16.
7
Cooperative gating and spatial organization of membrane proteins through elastic interactions.通过弹性相互作用实现膜蛋白的协同门控与空间组织
PLoS Comput Biol. 2007 May;3(5):e81. doi: 10.1371/journal.pcbi.0030081.
8
Bending mechanics and molecular organization in biological membranes.生物膜中的弯曲力学与分子组织
Annu Rev Phys Chem. 2007;58:697-717. doi: 10.1146/annurev.physchem.56.092503.141216.
9
Direct visualization of Escherichia coli chemotaxis receptor arrays using cryo-electron microscopy.利用冷冻电子显微镜直接观察大肠杆菌趋化性受体阵列。
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):3777-81. doi: 10.1073/pnas.0610106104. Epub 2007 Feb 26.
10
Positioning of chemosensory clusters in E. coli and its relation to cell division.大肠杆菌中化学感应簇的定位及其与细胞分裂的关系。
EMBO J. 2007 Mar 21;26(6):1615-23. doi: 10.1038/sj.emboj.7601610. Epub 2007 Mar 1.

通过二聚体的耦合三聚体实现极性化学感受器聚集。

Polar chemoreceptor clustering by coupled trimers of dimers.

作者信息

Endres Robert G

机构信息

Division of Molecular Biosciences and Centre for Integrated Systems Biology at Imperial College, Imperial College London, London, United Kingdom.

出版信息

Biophys J. 2009 Jan;96(2):453-63. doi: 10.1016/j.bpj.2008.10.021.

DOI:10.1016/j.bpj.2008.10.021
PMID:19167296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2716479/
Abstract

Receptors of bacterial chemotaxis form clusters at the cell poles, where clusters act as "antennas" to amplify small changes in ligand concentration. It is worthy of note that chemoreceptors cluster at multiple length scales. At the smallest scale, receptors form dimers, which assemble into stable timers of dimers. At a large scale, trimers form large polar clusters composed of thousands of receptors. Although much is known about the signaling properties emerging from receptor clusters, it is unknown how receptors localize at the cell poles and what the determining factors are for cluster size. Here, we present a model of polar receptor clustering based on coupled trimers of dimers, where cluster size is determined as a minimum of the cluster-membrane free energy. This energy has contributions from the cluster-membrane elastic energy, penalizing large clusters due to their high intrinsic curvature, and receptor-receptor coupling that favors large clusters. We find that the reduced cluster-membrane curvature mismatch at the curved cell poles leads to large and robust polar clusters, in line with experimental observation, whereas lateral clusters are efficiently suppressed.

摘要

细菌趋化性受体在细胞两极形成簇,这些簇充当“天线”以放大配体浓度的微小变化。值得注意的是,化学感受器在多个长度尺度上形成簇。在最小尺度上,受体形成二聚体,二聚体组装成稳定的二聚体三聚体。在大尺度上,三聚体形成由数千个受体组成的大的极性簇。尽管人们对受体簇产生的信号特性了解很多,但尚不清楚受体如何定位在细胞两极以及簇大小的决定因素是什么。在这里,我们提出了一个基于二聚体三聚体耦合的极性受体簇模型,其中簇大小被确定为簇 - 膜自由能的最小值。该能量来自簇 - 膜弹性能,由于大簇具有高固有曲率而对其进行惩罚,以及有利于大簇的受体 - 受体耦合。我们发现,弯曲细胞两极处簇 - 膜曲率失配的降低导致大而稳健的极性簇,这与实验观察结果一致,而侧向簇则被有效抑制。