Template-Based Assembly of Proteomic Short Reads For De Novo Antibody Sequencing and Repertoire Profiling

peer-reviewed · Analytical Chemistry · 2022

peer-reviewed · Analytical Chemistry · 2022. Douwe Schulte et al. Antibodies can target a vast molecular diversity of antigens. This is achieved by generating a complementary…
Date 2022-07-26
Type peer-reviewed
Venue Analytical Chemistry
Publisher American Chemical Society (ACS)
Contribution post-processor
DOI 10.1021/acs.analchem.2c01300
Citations (OpenAlex) 42
Venue 2-year citedness 7.10

Preprint version: Template-based assembly of proteomic short reads for de novo antibody sequencing and repertoire profiling (2022-03-08, bioRxiv)

Abstract

Antibodies can target a vast molecular diversity of antigens. This is achieved by generating a complementary diversity of antibody sequences through somatic recombination and hypermutation. A full understanding of the antibody repertoire in health and disease therefore requires dedicated de novo sequencing methods. Next-generation cDNA sequencing methods have laid the foundation of our current understanding of the antibody repertoire, but these methods share one major limitation in that they target the antibody-producing B-cells, rather than the functional secreted product in bodily fluids. Mass spectrometry-based methods offer an opportunity to bridge this gap between antibody repertoire profiling and bulk serological assays, as they can access antibody sequence information straight from the secreted polypeptide products. In a step to meeting the challenge of mass spectrometry (MS)-based antibody sequencing, we present a fast and simple software tool (Stitch) to map proteomic short reads to user-defined templates with dedicated features for both monoclonal antibody sequencing and profiling of polyclonal antibody repertoires. We demonstrate the use of Stitch by fully reconstructing two monoclonal antibody sequences with >98% accuracy (including I/L assignment); sequencing a Fab from patient serum isolated by reversed-phase liquid chromatography (LC) fractionation against a high background of homologous antibody sequences; sequencing antibody light chains from the urine of multiple-myeloma patients; and profiling the IgG repertoire in sera from patients hospitalized with COVID-19. We demonstrate that Stitch assembles a comprehensive overview of the antibody sequences that are represented in the dataset and provides an important first step toward analyzing polyclonal antibodies and repertoire profiling.

Authors

  1. Douwe Schulte · Netherlands Proteomics Centre, Utrecht University
  2. Weiwei Peng · Netherlands Proteomics Centre, Utrecht University
  3. Joost Snijder · Netherlands Proteomics Centre, Utrecht University

Methods and tools

  • Stitch: Assembles de novo peptides from Casanovo, PEAKS, pNovo and MaxNovo into full antibody sequences, and corrects the two error classes that assembly alone cannot: mass coincidences, where a different residue combination matches the same mass, and I/L ambiguity.

Data used

  • Anti-FLAG-M2 antibody sequencing (as deposited) · PXD023419
  • Template-based assembly of proteomic short reads for de novo antibody sequencing and repertoire profiling (as deposited) · PXD031941

Cites (14)

Cited by (25)

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