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趋化蛋白CheY的磷酸化与其在鞭毛马达处的活性之间的相关性。

Correlation between phosphorylation of the chemotaxis protein CheY and its activity at the flagellar motor.

作者信息

Barak R, Eisenbach M

机构信息

Department of Membrane Research and Biophysics, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Biochemistry. 1992 Feb 18;31(6):1821-6. doi: 10.1021/bi00121a034.

Abstract

Phosphorylation of the chemotaxis protein CheY by its kinase CheA appears to play a central role in the process of signal transduction in bacterial chemotaxis. It is presumed that the role is activation of CheY which results in clockwise (CW) flagellar rotation. The aim of this study was to determine whether this activity of CheY indeed depends on the protein being phosphorylated. Since the phosphorylation of CheY can be detected only in vitro, we studied the ability of CheY to cause CW rotation in an in vitro system, consisting of cytoplasm-free envelopes of Salmonella typhimurium or Escherichia coli having functional flagella. Envelopes containing just buffer rotated only counterclockwise. Inclusion of CheY caused 14% of the rotating envelopes to go CW. This fraction of CW-rotating envelopes was not altered when the phosphate potential in the envelopes was lowered by inclusion of ADP together with CheY in them, indicating that CheY has a certain degree of activity even without being phosphorylated. Attempts to increase the activity of CheY in the envelopes by phosphorylation were not successful. However, when CheY was inserted into partially-lysed cells (semienvelopes) under phosphorylating conditions, the number of CW-rotating cells increased 3-fold. This corresponds to more than a 100-fold increase in the activity of a single CheY molecule upon phosphorylation. It is concluded that nonphosphorylated CheY can interact with the flagellar switch and cause CW rotation, but that this activity is increased by at least 2 orders of magnitude by phosphorylation. This increase in activity requires additional cytoplasmic constituents, the identity of which is not yet known.

摘要

趋化蛋白CheY被其激酶CheA磷酸化似乎在细菌趋化作用的信号转导过程中起着核心作用。据推测,该作用是激活CheY,从而导致鞭毛顺时针(CW)旋转。本研究的目的是确定CheY的这种活性是否确实取决于被磷酸化的蛋白质。由于CheY的磷酸化只能在体外检测到,我们在一个体外系统中研究了CheY引起CW旋转的能力,该系统由具有功能性鞭毛的鼠伤寒沙门氏菌或大肠杆菌的无细胞质包膜组成。仅含有缓冲液的包膜仅逆时针旋转。加入CheY后,14%的旋转包膜变为CW旋转。当通过在包膜中加入ADP和CheY来降低包膜中的磷酸盐电位时,CW旋转包膜的这一比例没有改变,这表明CheY即使未被磷酸化也具有一定程度的活性。通过磷酸化来增加包膜中CheY活性的尝试未成功。然而,当在磷酸化条件下将CheY插入部分裂解的细胞(半包膜)中时,CW旋转细胞的数量增加了3倍。这相当于单个CheY分子磷酸化后活性增加了100多倍。得出的结论是,未磷酸化的CheY可以与鞭毛开关相互作用并引起CW旋转,但这种活性通过磷酸化至少增加2个数量级。这种活性的增加需要额外的细胞质成分,其身份尚不清楚。

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