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Applying high‐throughput methods to develop a purification process for a highly glycosylated protein
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Citations
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References
2012
Year
Purification ProcessEngineeringGlycobiologyPlate FormatProtein PurificationGlycoproteomicsFood ChemistryGas ChromatographyBioanalysisBiochemical EngineeringDownstream ProcessingAnalytical ChemistryLiquid ChromatographyClinical ChemistryPurification MethodChromatographyGlycosylationProtein GlycosylationFilter Plate FormatBiochemistryHigh‐throughput MethodsChromatographic AnalysisBiomolecular EngineeringNatural SciencesMicro-scale Chromatography FormatsBiotechnologyProtein EngineeringCarbohydrate-protein Interaction
Micro-scale chromatography formats are becoming more routinely used in purification process development because of their ability to rapidly screen large number of process conditions at a time with minimal material. Given the usual constraints that exist on development timelines and resources, these systems can provide a means to maximize process knowledge and process robustness compared to traditional packed column formats. In this work, a high-throughput, 96-well filter plate format was used in the development of the cation exchange and hydrophobic interaction chromatography steps of a purification process designed to alter the glycoform distribution of a small protein. The significant input parameters affecting process performance were rapidly identified for both steps and preliminary operating conditions were identified. These ranges were verified in a packed chromatography column in order to assess the ability of the 96-well plate to predict packed column performance. In both steps, the 96-well plate format consistently led to underestimated glycoform-enrichment levels and to overestimated product recovery rates compared to the column-based approach. These studies demonstrate that the plate format can be used as a screening tool to narrow the operating ranges prior to further optimization on packed chromatography columns.
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