AI Article Synopsis

  • Motile cilia are essential for cell movement and fluid flow, using bending waves that require coordination through radial spoke (RS) protein complexes and a central microtubule pair (CP).
  • The structure of the RS head was determined using advanced imaging techniques, revealing a flat, negatively charged surface and a rigid protein core.
  • Mutations in this core, linked to human diseases, affect the stability of the RS complex and its functionality, suggesting its role in regulating ciliary movement through interactions with the CP.

Article Abstract

Motile cilia power cell locomotion and drive extracellular fluid flow by propagating bending waves from their base to tip. The coordinated bending of cilia requires mechanoregulation by the radial spoke (RS) protein complexes and the microtubule central pair (CP). Despite their importance for ciliary motility across eukaryotes, the molecular function of the RSs is unknown. Here, we reconstituted the Chlamydomonas reinhardtii RS head that abuts the CP and determined its structure using single-particle cryo-EM to 3.1-Å resolution, revealing a flat, negatively charged surface supported by a rigid core of tightly intertwined proteins. Mutations in this core, corresponding to those involved in human ciliopathies, compromised the stability of the recombinant complex, providing a molecular basis for disease. Partially reversing the negative charge on the RS surface impaired motility in C. reinhardtii. We propose that the RS-head architecture is well-suited for mechanoregulation of ciliary beating through physical collisions with the CP.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855469PMC
http://dx.doi.org/10.1038/s41594-020-00519-9DOI Listing

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