“…The machine, in a 2-mile-long tunnel near Stanford, generates 120 pulses of hard or soft X-rays per second, containing about 1 Â 10 12 photons per 10 fs pulse, and, using purpose-built detectors, allows the diffraction pattern from each pulse to be read-out and saved. Broadly, three types of experiments were first attempted-those in which hydrated protein nanocrystals were sprayed across the pulsed beam (serial femtosecond nanocrystallography, SFX), those in which the hard X-ray beam of micrometre dimensions traverses many biomolecules in a liquid jet (fast solution scattering, FSS-see contributions by Haldrup [4], Mendez et al [5] and Pande et al [6]), and single particle (SP) imaging, in which a beam of submicrometre dimensions scatters from an SP such as a virus [7][8][9]. Before long many other experimental arrangements had also been tried during this exciting first 4 years, including fixed samples scanned across the beam for the study of two-dimensional membrane protein crystals [10], time-resolved SFX [11] (see also Moffat [12]), and new types of sample delivery devices, such as those based on the lipid cubic phase [13,14] and on electrospraying [15].…”