细菌鞭毛马达协调开关的时间尺度分离。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Guanhua Yue, Rongjing Zhang, Junhua Yuan
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引用次数: 0

摘要

细菌趋化信号通路的输出,细胞内调节因子CheY-P的水平,调节鞭毛马达的旋转方向,从而调节细菌的奔跑和翻滚行为。anE上的多个鞭毛马达。大肠细胞由一个共同的CheY-P细胞质池控制。CheY-P水平的波动被认为能够协调多个电机的开关。在这里,我们测量了一个细胞上两个马达之间旋转方向的相关性,发现它令人惊讶地表现出两个分离良好的时间尺度。我们发现缓慢的时间尺度(~ 6 s)可以用趋化适应酶的随机活性导致的CheY-P水平的缓慢波动来解释,而快速的时间尺度(~ 0.3 s)可以用CheY-P水平的随机脉冲状波动来解释,这可能是由于化学受体簇的活性。我们在相关测量的基础上提取了快速CheY-P脉冲的特性信息。CheY-P水平波动中的两个分离良好的时间尺度有助于协调细胞上的多个马达并增强细菌的趋化性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Timescale separation in the coordinated switching of bacterial flagellar motors.

The output of the bacterial chemotaxis signaling pathway, the level of the intracellular regulator CheY-P, modulates the rotation direction of the flagellar motor, thereby regulating bacterial run-and-tumble behavior. The multiple flagellar motors on anE. colicell are controlled by a common cytoplasmic pool of CheY-P. Fluctuation of the CheY-P level was thought to be able to coordinate the switching of multiple motors. Here, we measured the correlation of rotation directions between two motors on a cell, finding that it surprisingly exhibits two well separated timescales. We found that the slow timescale (∼6 s) can be explained by the slow fluctuation of the CheY-P level due to stochastic activity of the chemotactic adaptation enzymes, whereas the fast timescale (∼0.3 s) can be explained by the random pulse-like fluctuation of the CheY-P level, due probably to the activity of the chemoreceptor clusters. We extracted information on the properties of the fast CheY-P pulses based on the correlation measurements. The two well-separated timescales in the fluctuation of CheY-P level help to coordinate multiple motors on a cell and to enhance bacterial chemotactic performance.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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