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Chromosome Driven Spatial Patterning of Proteins in Bacteria

机译:细菌中染色体驱动的蛋白质空间格局

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The spatial patterning of proteins in bacteria plays an important role in many processes, from cell division to chemotaxis. In the asymmetrically dividing bacteria Caulobacter crescentus, a scaffolding protein, PopZ, localizes to both poles and aids the differential patterning of proteins between mother and daughter cells during division. Polar patterning of misfolded proteins in Escherechia coli has also been shown, and likely plays an important role in cellular ageing. Recent experiments on both of the above systems suggest that the presence of chromosome free regions along with protein multimerization may be a mechanism for driving the polar localization of proteins. We have developed a simple physical model for protein localization using only these two driving mechanisms. Our model reproduces all the observed patterns of PopZ and misfolded protein localization - from diffuse, unipolar, and bipolar patterns and can also account for the observed patterns in a variety of mutants. The model also suggests new experiments to further test the role of the chromosome in driving protein patterning, and whether such a mechanism is responsible for helping to drive the differentiation of the cell poles.
机译:细菌中蛋白质的空间模式在从细胞分裂到趋化性的许多过程中都起着重要作用。在不对称分裂的细菌Caulobacter crescentus中,一种支架蛋白PopZ位于两个极点,并有助于分裂过程中母细胞和子细胞之间蛋白质的差异模式。还显示了大肠杆菌中错误折叠的蛋白质的极性图谱,并且可能在细胞衰老中起重要作用。上述两个系统的最新实验表明,无染色体区域的存在以及蛋白质的多聚化可能是驱动蛋白质极性定位的一种机制。我们仅使用这两种驱动机制开发了用于蛋白质定位的简单物理模型。我们的模型从弥散,单极和双极模式中再现了PopZ和错误折叠的蛋白质定位的所有观察模式,也可以解释各种突变体中的观察模式。该模型还提出了新的实验,以进一步测试染色体在驱动蛋白质模式中的作用,以及这种机制是否负责帮助驱动细胞极的分化。

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