AI Article Synopsis

  • A new microfluidic system combines imaged capillary isoelectric focusing (iCIEF) with mass spectrometry (MS) detection, enabling efficient separation and analysis of protein isoforms in one assay.
  • The system allows for real-time monitoring of analyte focusing and quantification of charge isoforms, achieving results in under 15 minutes.
  • This innovative method can characterize 33 distinct molecular features of intact monoclonal antibodies, significantly improving the ability to assess multiple quality attributes in a single test.

Article Abstract

A microfluidic system has been designed that integrates both imaged capillary isoelectric focusing (iCIEF) separations and downstream MS detection into a single assay. Along with the construction of novel instrumentation and an innovative microfluidic chip, conversion to MS-compatible separation reagents has also been established. Incorporation of 280 nm absorbance iCIEF-MS analysis not only permits photometric quantitation of separated charge isoforms but also facilitates the direct monitoring of analyte focusing and mobilization in real-time. The outcome of this effort is a device with the unique ability to allow for both the characterization and identification of protein charge and mass isoforms in under 15 min. Acquisition, quantitation, and identification of highly resolved intact mAb charge isoforms along with their critical N-linked glycan pairs clearly demonstrate analytical utility of our innovative system. In total, 33 separate molecular features were characterized by the iCIEF-MS system representing a dramatic increase in the ability to monitor multiple intact mAb critical quality attributes in a single comprehensive assay. Unlike previously reported CIEF-MS results, relatively high ampholyte concentrations, of up to 4% v/v, were employed without impacting MS sensitivity, observed to be on the order of 1% composition.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972975PMC
http://dx.doi.org/10.1002/elps.201900325DOI Listing

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