posted on 2024-10-31, 09:15authored byBen Niu, Benjamin Lee, Wen Chen, Cristian Alberto, Karen Betancourt Moreira, Philip Compton, Kristoff Homan, Jason Pinckney, Yaxing Zhu, Michelle Vendel, Karl Wetterhorn, Shana Walrond, Esrath Santha, Amanda Horowitz, Nicole Zaubi, Jeffrey Johnson
Bispecific antibodies
(bsAbs) and multispecific antibodies
(msAbs)
represent a promising frontier in therapeutic antibody development,
offering unique capabilities not achievable with traditional monoclonal
antibodies. Despite their potential, significant challenges remain
due to their increased molecular complexity. One prominent challenge
is the correct assembly of light and heavy chains, as improper pairing
leads to mispaired or incompletely assembled species that lack therapeutic
efficacy and possess undesired properties, impairing the developability,
manufacturability, and safety. There is a critical need for rapid,
sensitive analytical tools to monitor and control these undesired
species and ensure the quality assessment of bsAbs and msAbs. To address
this need, we present a novel high-throughput, format-agnostic intact
mass workflow that significantly enhances the efficiency of detecting
and quantifying biotherapeutic products and related impurities. This
workflow integrates automated sample preparation, novel high-resolution
rapid mass detection powered by SampleStream-MS, and an advanced data
analysis pipeline. It offers increased throughput and data quality
while substantially reducing analysis turnover time and labor. This
was demonstrated in a pilot program where ∼800 multispecific
antibodies were processed in 10 working days. The article details
the evaluation and validation of our method, demonstrating its repeatability
and intermediate precision in terms of measurement accuracy and relative
quantification of various product-related species. We underscore the
transformative potential of this end-to-end high-throughput workflow
in expediting bispecific and multispecific antibody discovery, optimizing
production processes, and ensuring high-quality development and manufacturing
for therapeutic antibodies.