LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
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MP25<br />
Patrick Cooley<br />
Microfab Technologies, Inc.<br />
Plano, Texas<br />
patrick.cooley@microfab.com<br />
Where Laboratory Technologies Emerge and Merge<br />
PiezoLC Microdispenser for MALDI-TOF Analysis<br />
Co-Author(s)<br />
Ting Chen<br />
David Wallace<br />
Microfab Technologies, Inc.<br />
Femia Hopwood<br />
Andrew Gooley<br />
Proteome Systems, Ltd.<br />
Frantisek Svec. University of California, Berkeley<br />
The PiezoLC is an ink-jet system to deliver micro-volumes (0.1 to 100nL) of proteolysed peptides onto MALDI-TOF MS targets for<br />
subsequent mass spec analysis. A porous polymer monolith is located within the glass capillary of the ink-jet dispensing device to provide<br />
chromatographic separation of peptides. The peptide sample is loaded onto the integrated chromatography column (reversed phase) and an<br />
elution buffer separates the peptides, as the buffer passes through the column. The eluted peptides exit the orifice of the piezoelectric device<br />
in the form of drops and land onto a MALDI-TOF MS target plate preserving the chromatographic separation. The analysis of the peptides<br />
can then be performed at a later date and multiple times. The PiezoLC can be a useful tool for the identification and characterization<br />
of proteins from finite samples. Low-abundance proteins may not be detected during MS analysis, as they are commingled with highabundance<br />
proteins within protein digests and are obscured by ion suppression effects. The chromatographic separation of peptides<br />
by the PiezoLC can reduce ion suppression and improve resolution of MALDI-TOF MS analysis for applications, such as peptide mass<br />
fingerprinting. The PiezoLC separation of tryptic digests of Bovine Serum Albumin (BSA) resulted in a larger number of peptides identified in<br />
comparison to the control. This resulted in a higher degree of amino acid sequence coverage and improved protein identification.<br />
MP26<br />
Mary Cornett<br />
Innovadyne Technologies, Inc.<br />
Santa Rosa, California<br />
mcornett@innovadyne.com<br />
Co-Author<br />
Anca Rothe<br />
Innovadyne Technologies, Inc.<br />
Meeting the Liquid Handling Challenges of Low Volume Cell Assays<br />
One of the main challenges faced in the development of automated cell-based screening systems is the requirement to accurately and<br />
gently dispense low volumes of assay cells. Traditional and flow-through liquid handlers, commonly used in HTS applications, can dispense<br />
in a manner that results in shearing stress to live cells impacting viability. Additionally, typical instrument designs with mechanical valves<br />
included in the flow path, often contribute to imprecision through contamination and the clogging of flow paths. While the precision of<br />
solenoid-based dispensing systems has long been recognized, their widespread acceptance has been tempered with concern regarding<br />
performance or maintenance issues. Here, we discuss a solenoid-based system that overcomes these issues by exposing the solenoid<br />
valves only to deionized water at a constant pressure, allowing them to operate efficiently and effectively. In addition to improving<br />
robustness, the system design ensures that the aspirated sample never contacts moving parts and only encounters a very simple flow<br />
path, which is vital for the successful dispensing of live cells. We also present data from several homogenous cell assay types that<br />
demonstrate consistent maintenance of cell viability in a 1536-well format, as well as excellent dispensing precision of cells and several cell<br />
assay reagents in the low microliter dispense range.<br />
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