A wide variety of structural and biophysical techniques have been used
to study viral assembly pathways. For example, the use of three-dimen
sional electron microscopy has allowed the visualization of viral asse
mbly intermediates, as well as mature capsids. More detailed views of
small icosahedral viruses and viral proteins, such as proteases, have
been provided by X-ray crystallography. The combination of these struc
tural techniques represents a powerful new approach to investigating l
arge assemblies in atomic detail. The production of recombinant virus-
like particles has become another popular approach to studying viral a
ssembly.