Automated Ligand Purification Platform Accelerates Immunopeptidome Analysis by Mass Spectrometry.

J Proteome Res

Chan Zuckerberg Biohub, Stanford, California 94305, United States.

Published: January 2021

AI Article Synopsis

  • Major histocompatibility complex (MHC)-presented peptides (pMHC) are important for understanding T cell immune responses, which is crucial for developing targeted immunotherapies.
  • Recent advancements in mass spectrometry have made it a leading technology for discovering and quantifying pMHC, but sample preparation has been slow and labor-intensive.
  • A new high-throughput and automated platform allows for processing up to 96 samples in under 6 hours, identifying thousands of pMHC from a small number of cells, paving the way for improved immunopeptidome profiling and research in immunotherapy.

Article Abstract

Major histocompatibility complex (MHC)-presented peptides (pMHC) give insight into T cell immune responses, a critical step toward developing a new generation of targeted immunotherapies. Recent instrumentation advances have propelled mass spectrometry to being arguably the most robust technology for discovering and quantifying naturally presented pMHC from cells and tissues. However, sample preparation has remained a major limitation due to time-consuming and labor-intensive workflows. We developed a high-throughput and automated platform with enhanced speed, sensitivity, and reproducibility relative to prior studies. This pipeline is capable of processing up to 96 samples in 6 h or less yielding high-quality pMHC mixtures ready for mass spectrometry. Here, we describe our efforts to optimize purification and mass spectrometer parameters, ultimately allowing us to identify as many as almost 5000 pMHC I and 7400 pMHC II from as little as 2.5 × 10 Raji cells each. We believe that this platform will facilitate and accelerate immunopeptidome profiling and benefit clinical research for immunotherapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11391901PMC
http://dx.doi.org/10.1021/acs.jproteome.0c00464DOI Listing

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