An antibody-based biomarker discovery method by mass spectrometry sequencing of complementarity determining regions

peer-reviewed · Analytical and Bioanalytical Chemistry · 2011

peer-reviewed · Analytical and Bioanalytical Chemistry · 2011. Lennard J. M. Dekker et al. Autoantibodies are increasingly used as biomarkers in the detection of autoimmune disorders and cancer…
Date 2011-01-01
Type peer-reviewed
Venue Analytical and Bioanalytical Chemistry
Publisher Springer Science and Business Media LLC
Contribution downstream-application
DOI 10.1007/s00216-010-4361-9
Citations (OpenAlex) 36

Abstract

Autoantibodies are increasingly used as biomarkers in the detection of autoimmune disorders and cancer. Disease specific antibodies are generally detected by their binding to specific antigens. As an alternative approach, we propose to identify specific complementarity determining regions (CDR) of IgG that relate to an autoimmune disorder or cancer instead of the specific antigen(s). In this manuscript, we tested the technical feasibility to detect and identify CDRs of specific antibodies by mass spectrometry. We used a commercial pooled IgG preparation as well as purified serum IgG fractions that were spiked with different amounts of a fully human monoclonal antibody (adalimumab). These samples were enzymatically digested and analyzed by nanoLC Orbitrap mass spectrometry. In these samples, we were able to identify peptides derived from the CDRs of adalimumab. These peptides could be detected at an amount of 110 attomole, 5 orders of magnitude lower than the total IgG concentration in these samples. Using higher energy collision induced dissociation (HCD) fragmentation and subsequent de novo sequencing, we could successfully identify 50% of the detectable CDR peptides of adalimumab. In addition, we demonstrated that an affinity purification with anti-dinitrophenol (DNP) monoclonal antibody enhanced anti-DNP derived CDR detection in a serum IgG background. In conclusion, specific CDR peptides could be detected and sequenced at relatively low levels (attomole-femtomole range) which should allow the detection of clinically relevant CDR peptides in patient samples.

Authors

  1. Lennard J. M. Dekker · Erasmus MC, Erasmus University Rotterdam
  2. L. Zeneyedpour · Erasmus MC, Erasmus University Rotterdam
  3. Eric Brouwer · Erasmus MC, Erasmus University Rotterdam
  4. Martijn M. VanDuijn · Erasmus MC, Erasmus University Rotterdam
  5. Peter A. E. Sillevis Smitt · Erasmus MC, Erasmus University Rotterdam
  6. Theo M. Luider · Erasmus MC, Erasmus University Rotterdam

Methods and tools

  • CDR peptide biomarker sequencing: Tests detection of specific antibody CDR peptides in serum IgG backgrounds by Orbitrap MS, de novo sequencing half of the detectable adalimumab CDR peptides at attomole levels.

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