HFSP journal · 2007 · 323 citations · 63 references
Cilia and eukaryotic flagella are slender appendages that propel cells by oscillating bends driven by dynein motors, yet how motor activity is coordinated in space and time remains unclear. The study aims to determine how dynein motor coordination shapes flagellar beating by inferring motor mechanical properties from high‑precision Fourier‑averaged sperm shapes and proposing load‑dependent detachment as the underlying sliding control mechanism. The authors analyzed high‑precision Fourier‑averaged shapes of steadily beating bull sperm to infer motor mechanical properties, and proposed that load‑dependent detachment rates mediate sliding control. Experimental waveforms matched only a model where inter‑doublet sliding regulates motor activity, requiring significant basal microtubule sliding, indicating that basal compliance can reverse beat direction and that beat patterns arise from basal axoneme properties coupled with dynein mechanical feedback.
Cilia and eukaryotic flagella are slender cellular appendages whose regular beating propels cells and microorganisms through aqueous media. The beat is an oscillating pattern of propagating bends generated by dynein motor proteins. A key open question is how the activity of the motors is coordinated in space and time. To elucidate the nature of this coordination we inferred the mechanical properties of the motors by analyzing the shape of beating sperm: Steadily beating bull sperm were imaged and their shapes were measured with high precision using a Fourier averaging technique. Comparing our experimental data with wave forms calculated for different scenarios of motor coordination we found that only the scenario of interdoublet sliding regulating motor activity gives rise to satisfactory fits. We propose that the microscopic origin of such "sliding control" is the load dependent detachment rate of motors. Agreement between observed and calculated wave forms was obtained only if significant sliding between microtubules occurred at the base. This suggests a novel mechanism by which changes in basal compliance could reverse the direction of beat propagation. We conclude that the flagellar beat patterns are determined by an interplay of the basal properties of the axoneme and the mechanical feedback of dynein motors.
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