Cryo-EM of the 48-nm repeat of mammalian doublet microtubules revealed TEKTIP1 as a previously uncharacterized MIP positioned at the center of the tektin bundle, establishing its structural niche within the axoneme.
Evidence Cryo-EM atomic model reconstruction of bovine respiratory cilia doublet microtubules
- No functional data existed at this stage to determine whether TEKTIP1 is required for tektin bundle integrity
- Binding partners and interaction surfaces within the bundle were unresolved
- Role in motile versus primary cilia was not distinguished