Cryo‐electron tomography elucidates annular intraluminal configurations in Caenorhabditis elegans microtubules

Abstract

AbstractBackground informationMicrotubules serve as integral components in cellular operations such as cell division, intracellular trafficking, and cellular architecture. Composed of tubulin protein subunits, these hollow tubular structures have been increasingly elucidated through advanced cryo‐electron microscopy (Cryo‐EM), which has unveiled the presence of microtubule inner proteins (MIPs) within the microtubular lumen.ResultsIn the present investigation, we employ a synergistic approach incorporating high‐pressure freezing, cryo‐focused ion beam milling, and Cryo‐electron tomography (Cryo‐ET) to interrogate the in situ architecture of microtubules in Caenorhabditis elegans larvae. Our Cryo‐ET assessments across neuronal cilia and diverse tissue types consistently demonstrate the formation of annular configurations within the microtubular lumen.ConclusionsIn concert with recently characterized MIPs, our in situ observations within a living organism corroborate the hypothesis that intricate luminal assemblages exist within microtubule scaffolds. These findings necessitate further exploration into the molecular constituents and functional ramifications of these internal microtubular configurations in both cellular physiology and pathophysiology.