We demonstrate that the scanning tunneling microscope can be used to o
btain information about arrangement of tubulin subunits in the microtu
bule wall. Long rows of subunits with a periodicity of 3.8+/-0.4 nm we
re clearly visible in the images of microtubules, The separation betwe
en the rows of subunits was 4.8+/-0.4 nm. Close inspection of two imag
es revealed another periodicity of 7.8+/-0.4 nm in the contour levels
of the protofilaments. This indicates that alpha and beta tubulin mono
mers can be resolved, In these areas the monomers were arranged accord
ing to a 'B-type' lattice. Scanning tunneling microscope images confir
m that the lateral contacts between tubulin monomers in adjacent proto
filaments are compatible with a three-start, left-handed helix model.
This study demonstrates that scanning tunneling microscopy can give di
rect information on the structure and organization of macromolecular a
ssemblies and can complement the classical methods of electron microsc
opy and X-ray scattering.