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BL17B1 High-throughput Protein Crystallography Beamline
Scientific goals
With the development of protein expression and crystallization technology, the efficiency of obtaining protein crystals is increasing, and the requirements for measuring the crystal structure of proteins are becoming higher and higher. In addition to macromolecular protein crystals, high-throughput protein crystallography beamline (BL17B1) can also be used by small molecule crystallography users in the field of chemistry and materials science.
Techniques and methods
Single-wavelength anomalous diffraction (SAD), Multi-wavelength anomalous diffraction (MAD), Molecular replacement (MR), (multiple or single) isomorphous replacement (MIR/SIR), Patterson function, direct methods, X-ray single crystal diffraction.
Beamline Layout
Beamline specification
Photon Energy range | 5-20 keV |
Wavelength range | 0.62-2.48 ? |
Energy resolution (DE/E) | £3×10-4 |
Focused Beam size (FWHM) (H×V) (@300mA) | £150×80 mm2 (@12keV) |
Flux at sample (@300mA) | 33′1011 phs/s (@12keV) |
Focused beam divergence (H×V) (@300mA) | £1.5×0.2mrad2 |
Endstation
Equipment | Type | Capacity |
Diffractometer | ARINAX MD2 | SOC< 1μm (with Mini Kappa) |
Detector | Rayonix MX300 | 300 mm×300mm 73μm×73μm/pixel readout speed: 1s |
Cryosystem | LN2 Oxford Cryosystem 700 | 80-400K |
Sample mounting robot | Irelec CATS | storage capacity: 180 samples |
Distance between sample and detector | 90-800mm | |
Data processing software | HKL3000, APEX3, Olex2, etc. |