Open AccessA procedure for setting up high‐throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization
Author(s) -
Walter Thomas S.,
Mayo Chris J.,
Brown James,
Carter Lester,
Diprose Jonathan M.,
Siebold Christian,
Pickford Mike G.,
Sutton Geoff C.,
Berrow Nick S.,
Berry Ian M.,
StewartJones Guillaume B. E.,
Grimes Jonathan M.,
Stammers David K.,
Jones E. Yvonne,
Esnouf Robert M.,
Owens Ray J.,
Stuart David I.,
Harlos Karl
Publication year - 2005
Publication title -
acta crystallographica section d
Language(s) - English
Resource type - Journals
ISSN - 1399-0047
DOI - 10.1107/s0907444905007808
Subject(s) - crystallization , workflow , throughput , protein crystallization , computer science , interface (matter) , process engineering , chemical engineering , engineering , database , operating system , bubble , maximum bubble pressure method , wireless
Crystallization trials at the Division of Structural Biology in Oxford are now almost exclusively carried out using a high‐throughput workflow implemented in the Oxford Protein Production Facility. Initial crystallization screening is based on nanolitre‐scale sitting‐drop vapour‐diffusion experiments (typically 100 nl of protein plus 100 nl of reservoir solution per droplet) which use standard crystallization screening kits and 96‐well crystallization plates. For 294 K crystallization trials the barcoded crystallization plates are entered into an automated storage system with a fully integrated imaging system. These plates are imaged in accordance with a pre‐programmed schedule and the resulting digital data for each droplet are harvested into a laboratory information‐management system (LIMS), scored by crystal recognition software and displayed for user analysis via a web‐based interface. Currently, storage for trials at 277 K is not automated and for imaging the crystallization plates are fed by hand into an imaging system from which the data enter the LIMS. The workflow includes two procedures for nanolitre‐scale optimization of crystallization conditions: (i) a protocol for variation of pH, reservoir dilution and protein:reservoir ratio and (ii) an additive screen. Experience based on 592 crystallization projects is reported.