Sampling the diffraction pattern of a finite specimen more finely than the
Nyquist frequency (the inverse of the size of the diffracting specimen) cor
responds to surrounding the electron density of the specimen with a no-dens
ity region. When the no-density region is bigger than the electron-density
region, sufficient information is recorded so that the phase information ca
n be retrieved from the oversampled diffraction pattern, at least in princi
ple. By employing an iterative algorithm, the phase information from the ov
ersampled diffraction pattern of a micrometre-sized test specimen has been
successfully retrieved. This method is believed to be able to open a door f
or high-resolution three-dimensional structure determination of complex and
non-crystalline biological specimens, i.e. whole cells and sub-micrometre
molecular clusters and micrometre-sized protein crystals. With the possible
appearance in the future of X-ray free-electron lasers, it may become poss
ible to image single molecules by recording diffraction patterns before rad
iation damage manifests itself.