De novo sequencing and construction of a unique antibody for the recognition of alternative conformations of cytochrome c in cells

peer-reviewed · Proceedings of the National Academy of Sciences · 2022

peer-reviewed · Proceedings of the National Academy of Sciences · 2022. Florencia Tomasina et al. Cytochrome c (cyt c) can undergo reversible conformational changes under biologically relevant conditions…
Date 2022-11-22
Type peer-reviewed
Venue Proceedings of the National Academy of Sciences
Publisher National Academy of Sciences
Contribution downstream-application
DOI 10.1073/pnas.2213432119
Citations (OpenAlex) 5
Venue 2-year citedness 8.56

Abstract

Cytochrome c (cyt c) can undergo reversible conformational changes under biologically relevant conditions. Revealing these alternative cyt c conformers at the cell and tissue level is challenging. A monoclonal antibody (mAb) identifying a key conformational change in cyt c was previously reported, but the hybridoma was rendered nonviable. To resurrect the mAb in a recombinant form, the amino-acid sequences of the heavy and light chains were determined by peptide mapping-mass spectrometry-bioinformatic analysis and used to construct plasmids encoding the full-length chains. The recombinant mAb (R1D3) was shown to perform similarly to the original mAb in antigen-binding assays. The mAb bound to a variety of oxidatively modified cyt c species (e.g., nitrated at Tyr74 or oxidized at Met80), which lose the sixth heme ligation (Fe-Met80); it did not bind to several cyt c phospho- and acetyl-mimetics. Peptide competition assays together with molecular dynamic studies support that R1D3 binds a neoepitope within the loop 40-57. R1D3 was employed to identify alternative conformations of cyt c in cells under oxidant- or senescence-induced challenge as confirmed by immunocytochemistry and immunoaffinity studies. Alternative conformers translocated to the nuclei without causing apoptosis, an observation that was further confirmed after pinocytic loading of oxidatively modified cyt c to B16-F1 cells. Thus, alternative cyt c conformers, known to gain peroxidatic function, may represent redox messengers at the cell nuclei. The availability and properties of R1D3 open avenues of interrogation regarding the presence and biological functions of alternative conformations of cyt c in mammalian cells and tissues.

Authors

  1. Florencia Tomasina
  2. Jennyfer Martínez
  3. Ari Zeida
  4. María Laura Chiribao
  5. Verónica Demicheli
  6. Agustín Correa
  7. Celia Quijano
  8. Laura Castro
  9. Robert H. Carnahan
  10. Paige Vinson
  11. Matt Goff
  12. Tracy Cooper
  13. W. Hayes McDonald · Oak Ridge National Laboratory, Vanderbilt University
  14. Natalie Castellana
  15. Luciana Hannibal
  16. Paul T. Morse
  17. Junmei Wan
  18. Maik Hüttemann
  19. Ronald Jemmerson
  20. Lucía Piacenza
  21. Rafael Radi

Methods and tools

  • Conformation-specific cytochrome c antibody: Sequences de novo an antibody that recognises an alternative conformer of cytochrome c, so that conformational states can be detected in cells and tissue, and rebuilds it from that sequence.

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