Freeze-fracture electron microscopy is especially useful for investigation
of lipid structures by the advantageous fracture course within hydrophobic
zones. Freezing is, on the other hand, a restriction because the structures
of lamellar and non-lamellar phase states with disordered acyl chains (L-a
lpha H-II, cubic) are difficult to preserve. An important aspect of this me
thod is therefore the lipid structure of phase states with ordered acyl cha
ins (crystal, gel), and with a different degree of hydration. Freeze-fractu
re of pure lipid systems creates a valid representation of the structure of
non-lamellar phases and of the general structure of the "lamellar" lipid b
ilayer, and lamellar phases with characteristic deformations (ripples, curv
atures, plane sectors) can be identified. Fracture through the hydrophobic
bilayer centre of biological membranes reveals characteristic protein compo
nents, the intramembraneous particles (IMPs). The lateral distribution of t
he IMPs is a helpful marker for fluid and rigid phase states, also without
deformation of the lamella. The overall history and the present state of kn
owledge concerning the different structures revealed by the freeze-fracture
and freeze-etch techniques in lipid systems, and to a limited extent in bi
ological membranes, is reviewed, taking into account studies from our own l
aboratory. (C) 2001 Elsevier Science Ltd. All rights reserved.