Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle, United Kingdom.
J Bacteriol. 2018 Apr 9;200(9). doi: 10.1128/JB.00658-17. Print 2018 May 1.
Chemoreceptors are localized at the cell poles of and other rod-shaped bacteria. Over the years, different mechanisms have been put forward to explain this polar localization, including stochastic clustering, membrane curvature-driven localization, interactions with the Tol-Pal complex, and nucleoid exclusion. To evaluate these mechanisms, we monitored the cellular localization of the aspartate chemoreceptor Tar in different deletion mutants. We did not find any indication for either stochastic cluster formation or nucleoid exclusion. However, the presence of a functional Tol-Pal complex appeared to be essential to retain Tar at the cell poles. Interestingly, Tar still accumulated at midcell in and in deletion mutants. In these mutants, the protein appears to gather at the base of division septa, a region characterized by strong membrane curvature. Chemoreceptors, like Tar, form trimers of dimers that bend the cell membrane due to a rigid tripod structure. The curvature approaches the curvature of the cell membrane generated during cell division, and localization of chemoreceptor tripods at curved membrane areas is therefore energetically favorable, as it lowers membrane tension. Indeed, when we introduced mutations in Tar that abolish the rigid tripod structure, the protein was no longer able to accumulate at midcell or the cell poles. These findings favor a model where chemoreceptor localization in is driven by strong membrane curvature and association with the Tol-Pal complex. Bacteria have exquisite mechanisms to sense and adapt to the environment they live in. One such mechanism involves the chemotaxis signal transduction pathway, in which chemoreceptors specifically bind certain attracting or repelling molecules and transduce the signals to the cell. In different rod-shaped bacteria, these chemoreceptors localize specifically to cell poles. Here, we examined the polar localization of the aspartate chemoreceptor Tar in and found that membrane curvature at cell division sites and the Tol-Pal protein complex localize Tar at cell division sites, the future cell poles. This study shows how membrane curvature can guide localization of proteins in a cell.
化感受体位于 和其他杆状细菌的细胞极。多年来,人们提出了不同的机制来解释这种极定位,包括随机聚类、膜曲率驱动的定位、与 Tol-Pal 复合物的相互作用以及核体排斥。为了评估这些机制,我们监测了天冬氨酸化感受体 Tar 在不同缺失突变体中的细胞定位。我们没有发现任何随机聚类形成或核体排斥的迹象。然而,功能性 Tol-Pal 复合物的存在似乎对于将 Tar 保留在细胞极至关重要。有趣的是,Tar 仍然在 和缺失突变体中积累在细胞中部。在这些突变体中,该蛋白似乎聚集在分裂隔膜的底部,该区域的膜曲率很强。化感受体,如 Tar,形成由刚性三脚架结构使细胞膜弯曲的二聚体三聚体。曲率接近细胞分裂过程中产生的细胞膜曲率,因此化感受体三脚架在弯曲的膜区域的定位在能量上是有利的,因为它降低了膜张力。事实上,当我们引入使 Tar 失去刚性三脚架结构的突变时,该蛋白就不再能够在细胞中部或细胞极积累。这些发现支持了这样一种模型,即 中的化感受体定位是由强膜曲率和与 Tol-Pal 复合物的关联驱动的。细菌具有敏锐的机制来感知和适应其所处的环境。其中一种机制涉及趋化性信号转导途径,其中化感受体特异性地结合某些吸引或排斥分子,并将信号转导到细胞中。在不同的杆状细菌中,这些化感受体特异性地定位到细胞极。在这里,我们研究了 中天冬氨酸化感受体 Tar 的极定位,发现细胞分裂位点的膜曲率和 Tol-Pal 蛋白复合物将 Tar 定位在细胞分裂位点,即未来的细胞极。这项研究展示了膜曲率如何在细胞中引导蛋白质的定位。