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Part 1 - CESI-MS for Characterization of Intact Proteins Norman E. Skelly Award for excellence in Separation Science the Vernon A. Stenger award for ...
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CESI-MS analysis of intact proteins and polypeptides Key Benefits: Easy 3-step covalent coating procedure Efficient robust reproducible separation of intact proteins using positively-charged coating High efficiency electrospray ionization in the low-nanoflow regime CESI capillary can be re-coated
(RP-LC-MS) has become a primary technique for antibody characterization and particularly in early stage development as MS can provide critical insights on the protein integrity and purity However the charge variant analysis of intact biopharmaceuticals by conventional RP-LC-MS is not possible
CESI-MS setup for intact protein analysis was evaluated by comparing the MS spectra measured at different flow rates Figure 4 compares the MS spectra from the analysis of an intact therapeutic monoclonal antibody (Humira) by simple infusion using the CESI sprayer at ultra-low (A: 20 nL/min) and low (B: 250 nL/min) flow rates
CESI-MS data were analyzed using Bruker Daltonics Data Analysis software Base-peak electropherograms (BPE) were constructed in the range m/z 1000-3000 For determination of detection linearity
CESI is the method of choice for high-resolution separation of polar metabolites peptides and proteins rich in particular post-translational modifications (such as glycosylation citrullination methylation and phosphorylation) Separate Charged / Polar Molecules and Proteins in High Resolution
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