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Using a Synthetic Probe to Study the Robustness of the Segregation Process of Protein Aggregates in Escherichia coli

机译:使用合成探针研究蛋白质聚集体在大肠杆菌中的分离过程的鲁棒性

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Even though the processes of protein production and folding are not immune to errors, Escherichia coli lineages are capable to maintain a stable cell lineage, provided viable environmental conditions. One of the internal processes that makes this possible consists of segregating unwanted protein aggregates to the cell poles by nucleoid exclusion, which, combined with cell divisions, generates asymmetries in the aging process of the population, with some individuals aging faster while others exhibit rejuvenation. A recent study showed that this process is not immune to sub-optimal temperature conditions due to increased cytoplasm viscosity, which weakens the anisotropy in aggregate displacements at the nucleoid borders. This was made possible by the usage of a synthetic fluorescent probe, consisting of a RNA sequence with multiple binding sites for the MS2-GFP synthetic protein, which can be tracked in time-lapse microscopy images. Here we provide a description of the findings from these measurements and investigate with an In Silico model the consequences in the context of cell lineages.
机译:尽管蛋白质产生和折叠的过程不受误差,但大肠杆菌谱系能够保持稳定的细胞谱系,提供可行的环境条件。使得这种可能的内部方法之一包括通过核排斥将不需要的蛋白质聚集体分离,这与细胞分裂结合,在人口的老化过程中产生不对称,一些人衰老,而其他人则表现出恢复活力。最近的一项研究表明,由于细胞质粘度增加,该方法不会因细胞质粘度增加而不受次优温条件的影响,这削弱了核邻核边界的骨料位移中的各向异性。这是通过使用合成荧光探针的用途可以实现,该探针由具有用于MS2-GFP合成蛋白的多个结合位点的RNA序列,可以在延时显微镜图像中跟踪。在这里,我们提供了这些测量结果的描述,并在Silico模型中调查了细胞谱系的背景下的后果。

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