Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Mol Syst Biol. 2010 Jun 22;6:382. doi: 10.1038/msb.2010.37.
The Escherichia coli chemotaxis-signaling pathway computes time derivatives of chemoeffector concentrations. This network features modules for signal reception/amplification and robust adaptation, with sensing of chemoeffector gradients determined by the way in which these modules are coupled in vivo. We characterized these modules and their coupling by using fluorescence resonance energy transfer to measure intracellular responses to time-varying stimuli. Receptor sensitivity was characterized by step stimuli, the gradient sensitivity by exponential ramp stimuli, and the frequency response by exponential sine-wave stimuli. Analysis of these data revealed the structure of the feedback transfer function linking the amplification and adaptation modules. Feedback near steady state was found to be weak, consistent with strong fluctuations and slow recovery from small perturbations. Gradient sensitivity and frequency response both depended strongly on temperature. We found that time derivatives can be computed by the chemotaxis system for input frequencies below 0.006 Hz at 22 degrees C and below 0.018 Hz at 32 degrees C. Our results show how dynamic input-output measurements, time honored in physiology, can serve as powerful tools in deciphering cell-signaling mechanisms.
大肠杆菌趋化信号转导途径计算化学引诱剂浓度的时间导数。该网络具有信号接收/放大和稳健适应的模块,通过这些模块在体内的耦合方式来确定化学引诱剂梯度的检测。我们通过使用荧光共振能量转移来测量对时变刺激的细胞内响应来表征这些模块及其耦合。通过阶跃刺激来表征受体的敏感性,通过指数斜坡刺激来表征梯度敏感性,通过指数正弦波刺激来表征频率响应。对这些数据的分析揭示了连接放大和适应模块的反馈传递函数的结构。在稳态附近的反馈被发现很弱,这与强波动和从小的扰动中缓慢恢复一致。梯度敏感性和频率响应都强烈依赖于温度。我们发现,趋化系统可以在 22°C 下低于 0.006 Hz 和 32°C 下低于 0.018 Hz 的输入频率下计算时间导数。我们的结果表明,动态输入-输出测量,在生理学中由来已久,可以作为破译细胞信号机制的强大工具。