In 1974, optical diffraction and image analysis indicated that tubulin
dimers in the cylindrically complete A-tubule of flagellar doublet mi
crotubules are arranged with helical symmetry, while those in the inco
mplete B-tubule associate differently. Recently, electron micrographs
of reassembled brain microtubules decorated with kinesin heads have sh
own that the tubulin dimers there are arranged as in the B-tubule. The
lack of symmetry of microtubules assembled in vitro prompts Linda Amo
s to speculate here that the assembly process in vitro may differ from
that occurring in the cell.