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Single
Molecule Imaging
Keith Hodgson
Stanford Synchrotron Radiation Laborat
ory/SLAC,
2575 Sand Hill Road, MS 69, Menlo Park, CA 94025
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X-ray
based methods are one of the premier tools for determining structure
of a broad range of materials at the atomic level. Such information,
including that on biological materials, has driven discovery and advances
in many ways that range from gaining fundamental insights into structure-function
relations to guiding the development of new materials based upon knowledge
of structure. Diffraction of x-rays from single crystals of macromolecules
has provided the vast majority of such information currently available
today for biological systems. Other techniques like NMR and electron
microscopy provide complementary information. One of the "limitatio
ns"
of x-ray diffraction is the requirement for single crystals. While
EM does not have this requirement, in practice cryo-EM approaches
have not been able to achieve atomic resolution. The ability to "image"
biomolecules at high resolution would be a significant advance. This
brief talk will describe a new approach to that goal based upon the
use of ultra bright x-rays that would become available from an X-ray
free electron laser such as the proposed LCLS at Stanford. Simulations
indicate that such a source could be used to obtain atomic or near-atomic
resolution structures from non- periodic samples, including single
biomolecules. The nature of the experiment is such that there is also
a more direct way of obtaining phase information that is necessary
to recover the real space image from the intensity information that
is recorde
d in diffraction space. This talk will briefly describe
this new approach. |
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