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pubmed-article:17889820pubmed:abstractTextSurface plasmon resonance imaging systems, such as Flexchip from Biacore, are capable of monitoring hundreds of reaction spots simultaneously within a single flow cell. Interpreting the binding kinetics in a large-format flow cell presents a number of potential challenges, including accounting for mass transport effects and spot-to-spot sample depletion. We employed a combination of computer simulations and experimentation to characterize these effects across the spotted array and established that a simple two-compartment model may be used to accurately extract intrinsic rate constants from the array under mass transport-limited conditions. Using antibody systems, we demonstrate that the spot-to-spot variability in the binding kinetics was <9%. We also illustrate the advantage of globally fitting binding data from multiple spots within an array for a system that is mass transport limited.lld:pubmed
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pubmed-article:17889820pubmed:year2008lld:pubmed
pubmed-article:17889820pubmed:articleTitleExtracting kinetic rate constants from surface plasmon resonance array systems.lld:pubmed
pubmed-article:17889820pubmed:affiliationCenter for Biomolecular Interaction Analysis, School of Medicine, University of Utah, Salt Lake City, UT 84132, USA.lld:pubmed
pubmed-article:17889820pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17889820pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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