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Imaging Molecules using X-ray free-electron lasers
Henry Chapman (DESY)
building 2a, seminar room 2, 16.45 h
The pulses from X-ray free-electron lasers are a billion times brighter than the brightest synchrotron beams available today. The short, intense X-ray laser pulses are so short they can out-run radiation damage, overcoming a major bottleneck for protein crystallography. I will describe the new methodologies for unravelling the structures of macromolecules using these sources, and show some examples of how we can track their motions in time. Very soon the European XFEL will begin operations and the new capabilities of that source should bring even greater progress to the field of structural biology.
