The Upgrade Programme for the Structural Biology beam lines at the European Synchrotron Radiation Facility - High throughput sample evaluation and automation

• Published in: Journal of physics. Conference series Vol. 425; pp. 1 - 4
• Main Authors: Theveneau, P, Baker, R, Barrett, R, Beteva, A, Bowler, M W, Carpentier, P, Caserotto, H, de Sanctis, D, Dobias, F, Flot, D
• Format: Journal Article
• Language: English
• Published: 01.01.2013
• Subjects: Automation; Biology; Complexity; Construction; Diffraction; Heterogeneity; Particle physics
• ISSN: 1742-6588; 1742-6596
• DOI: 10.1088/1742-6596/425/1/012001

Automation and advances in technology are the key elements in addressing the steadily increasing complexity of Macromolecular Crystallography (MX) experiments. Much of this complexity is due to the interand intra-crystal heterogeneity in diffraction quality often observed for crystals of multi-component macromolecular assemblies or membrane proteins. Such heterogeneity makes high-throughput sample evaluation an important and necessary tool for increasing the chances of a successful structure determination. The introduction at the ESRF of automatic sample changers in 2005 dramatically increased the number of samples that were tested for diffraction quality. This "first generation" of automation, coupled with advances in software aimed at optimising data collection strategies in MX, resulted in a three-fold increase in the number of crystal structures elucidated per year using data collected at the ESRF. In addition, sample evaluation can be further complemented using small angle scattering experiments on the newly constructed bioSAXS facility on BM29 and the micro-spectroscopy facility (ID29S). The construction of a second generation of automated facilities on the MASSIF (Massively Automated Sample Screening Integrated Facility) beam lines will build on these advances and should provide a paradigm shift in how MX experiments are carried out which will benefit the entire Structural Biology community.