Control of Helical Navigation by Three-Dimensional Flagellar Beating

Helical swimming is a ubiquitous strategy for motile cells to generate self-gradients for environmental sensing. The model biflagellate Chlamydomonas reinhardtii rotates at a constant 1-2 Hz as it swims, but the mechanism is unclear. Here, we show unequivocally that the rolling motion derives from a persistent, nonplanar flagellar beat pattern. This is revealed by high-speed imaging and micromanipulation of live cells. We construct a fully 3D model to relate flagellar beating directly to the free-swimming trajectories. For realistic geometries, the model reproduces both the sense and magnitude of the axial rotation of live cells. We show that helical swimming requires further symmetry breaking between the two flagella. These functional differences underlie all tactic responses, particularly phototaxis. We propose a control strategy by which cells steer toward or away from light by modulating the sign of biflagellar dominance.

Automated summary

This study demonstrates that the rolling motion of the biflagellate Chlamydomonas reinhardtii during swimming is derived from a nonplanar flagellar beat pattern, and a 3D model is constructed to explain this phenomenon. It is found that helical swimming requires further symmetry breaking between the two flagella, which is crucial for phototactic responses.