Logarithmic Sensing in Escherichia coli Bacterial Chemotaxis

被引:202
作者
Kalinin, Yevgeniy V. [2 ]
Jiang, Lili [3 ,4 ]
Tu, Yuhai [1 ]
Wu, Mingming [2 ,5 ]
机构
[1] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA
[2] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
[3] Peking Univ, Sch Phys, Beijing 100871, Peoples R China
[4] Peking Univ, Ctr Theoret Biol, Beijing 100871, Peoples R China
[5] Cornell Univ, Sibley Sch Mech & Aerosp Engn, Ithaca, NY 14853 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
QUANTITATIVE-ANALYSIS; MICROFLUIDIC DEVICE; PERFECT ADAPTATION; PARTICLE TRACKING; MODEL; SENSITIVITY; RECEPTOR; GRADIENTS; RESPONSES; FEEDBACK;
D O I
10.1016/j.bpj.2008.10.027
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We studied the response of swimming Escherichia coli(E. coli) bacteria in a comprehensive set of well-controlled chemical concentration gradients using a newly developed microfluidic device and cell tracking imaging technique. In parallel, we carried out a multi-scale theoretical modeling of bacterial chemotaxis taking into account the relevant internal signaling pathway dynamics, and predicted bacterial chemotactic responses at the cellular level. By measuring the E. coli cell density profiles across the microfluidic channel at various spatial gradients of ligand concentration grad[L] and the average ligand concentration ([L]) over bar near the peak chemotactic response region, we demonstrated unambiguously in both experiments and model simulation that the mean chemotactic drift velocity of E. coli cells increased monotonically with grad [L]/([L]) over bar or similar to grad(log[L]-that is E. coli cells sense the spatial gradient of the logarithmic ligand concentration. The exact range of the log-sensing regime was determined. The agreements between the experiments and the multi-scale model simulation verify the validity of the theoretical model, and revealed that the key microscopic mechanism for logarithmic sensing in bacterial chemotaxis is the adaptation kinetics, in contrast to explanations based directly on ligand occupancy.
引用
收藏
页码:2439 / 2448
页数:10
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