A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.

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 experiment...

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Main Authors: Walter, T, Diprose, J, Mayo, C, Siebold, C, Pickford, MG, Carter, L, Sutton, G, Berrow, N, Brown, J, Berry, I, Stewart-Jones, G, Grimes, J, Stammers, D, Esnouf, R, Jones, E, Owens, R, Stuart, D, Harlos, K
Format: Journal article
Language:English
Published: 2005
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author Walter, T
Diprose, J
Mayo, C
Siebold, C
Pickford, MG
Carter, L
Sutton, G
Berrow, N
Brown, J
Berry, I
Stewart-Jones, G
Grimes, J
Stammers, D
Esnouf, R
Jones, E
Owens, R
Stuart, D
Harlos, K
author_facet Walter, T
Diprose, J
Mayo, C
Siebold, C
Pickford, MG
Carter, L
Sutton, G
Berrow, N
Brown, J
Berry, I
Stewart-Jones, G
Grimes, J
Stammers, D
Esnouf, R
Jones, E
Owens, R
Stuart, D
Harlos, K
author_sort Walter, T
collection OXFORD
description 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.
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spelling oxford-uuid:cc9a4769-bb6f-4c2d-a2f0-ef84bf269d042022-03-27T07:23:09ZA procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cc9a4769-bb6f-4c2d-a2f0-ef84bf269d04EnglishSymplectic Elements at Oxford2005Walter, TDiprose, JMayo, CSiebold, CPickford, MGCarter, LSutton, GBerrow, NBrown, JBerry, IStewart-Jones, GGrimes, JStammers, DEsnouf, RJones, EOwens, RStuart, DHarlos, KCrystallization 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.
spellingShingle Walter, T
Diprose, J
Mayo, C
Siebold, C
Pickford, MG
Carter, L
Sutton, G
Berrow, N
Brown, J
Berry, I
Stewart-Jones, G
Grimes, J
Stammers, D
Esnouf, R
Jones, E
Owens, R
Stuart, D
Harlos, K
A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title_full A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title_fullStr A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title_full_unstemmed A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title_short A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimization.
title_sort procedure for setting up high throughput nanolitre crystallization experiments crystallization workflow for initial screening automated storage imaging and optimization
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