omation mbers - Society for Laboratory Automation and Screening
omation mbers - Society for Laboratory Automation and Screening
omation mbers - Society for Laboratory Automation and Screening
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9:00 am Wednesday, February 4 Proteomics – Structural Room B1<br />
John A. Adams<br />
RoboDesign International, Inc.<br />
5120 Pasteur Court<br />
Carlsbad, Cali<strong>for</strong>nia 92008<br />
jadams@robodesign.com<br />
Automated Protein Crystallization System<br />
85<br />
Co-Author(s)<br />
Janet M. Newman, David W. Jewell,<br />
John K. Hoffman, M<strong>and</strong>el W. Mickley<br />
A complete, intermediate-sized (1100 plates), dual temperature, automated protein crystallization plat<strong>for</strong>m<br />
consisting of automated small-volume pipetting, automatic plate incubation, storage <strong>and</strong> retrieval, automatic drop<br />
imaging, database cataloging, analysis <strong>and</strong> classification, plus a closed-loop crystal trial experiment <strong>and</strong> trial<br />
optimization database that seamlessly connects all of the sub-system software <strong>and</strong> hardware. This system enables<br />
users to set up initial screens using st<strong>and</strong>ard screen blocks or to make custom initial screens, automatically make<br />
the experimental plates <strong>and</strong> have them transferred into incubation, imaged, analyzed, <strong>and</strong> classified based upon a<br />
user defined schedule. These results <strong>for</strong>m the basis <strong>for</strong> an intelligent plat<strong>for</strong>m that can be used to more quickly <strong>and</strong><br />
efficiently determine optimal protein crystal growth conditions.<br />
9:30 am Wednesday, February 4 Proteomics – Structural Room B1<br />
Brent Segelke<br />
Lawrence Livermore National <strong>Laboratory</strong><br />
7000 East Avenue<br />
Livermore, Cali<strong>for</strong>nia 94551<br />
segelke1@llnl.gov<br />
Automated Combinatorial Protein Crystallization <strong>Screening</strong><br />
Co-Author(s)<br />
Dominique Toppani, Tim Lekin, Bernhard Rupp<br />
Lawrence Livermore National <strong>Laboratory</strong><br />
Mary Cornett, Joel McComb<br />
Innovadyne Technologies, Inc.<br />
By considering crystal screening as a sampling problem, we have previously demonstrated, by probability theory,<br />
the inherent efficiency of stochastic combinatorial screening (Segelke, J. Crystal Growth 2000). While efficient in<br />
principal, stochastic combinatorial screening is difficult to automate in practice. Robotic liquid h<strong>and</strong>ling instruments<br />
are generally designed <strong>for</strong> high throughput mother-daughter transfers or <strong>for</strong> lower throughput, though versatile, rearraying.<br />
A new 96-tip, non-contact, liquid h<strong>and</strong>ling instrument by Innovdyne makes high throughput automated<br />
crystallization screening, on the fly, possible. The instrument is equipped with 96, independently actuated, noncontact,<br />
nano-dispensing tips. The Independent actuation enables any source any destination liquid h<strong>and</strong>ling.<br />
With a software experimental design engine, CRYSTOOL, aspirate/dispense operations are generated on the<br />
fly <strong>and</strong> passed to the instrument at run-time. Stock reagents arrayed in 96-well deep well blocks are aspirated<br />
simultaneously <strong>and</strong> dispensed in the r<strong>and</strong>om order <strong>and</strong> volume prescribed by worklists generated by the design<br />
engine. The instrument also maintains high precision over a broad range of volumes <strong>and</strong> viscosities, delivering<br />
exceptional versatility <strong>for</strong> types, concentrations, <strong>and</strong> ratios of components used in custom combinatorial screens.<br />
The same instrument can be used <strong>for</strong> rapid setup of vapor diffusion or microbatch crystallization experiments from<br />
premade screens or <strong>for</strong> the setup of grid optimization screens.<br />
PODIUM ABSTRACTS