Development of an enhanced anti-pan-N-formylmethionine-specific antibody
Both bacterial and eukaryotic ribosomes can initiate protein synthesis with formylmethionine (fMet), but detecting fMet-bearing peptides and fMet-bearing proteins has been challenging due to the lack of effective anti-pan-fMet antibodies. Previously, we developed a polyclonal anti-fMet antibody using a fMet-Gly-Ser-Gly-Cys pentapeptide that detects those fMet-bearing peptides and fMet-bearing proteins regardless of their sequence context. In this study, we significantly improved the antibody's specificity and affinity by using a mixture of fMet-Xaa-Cys tripeptides (Xaa, any of the 20 amino acids) as the immunogen. This newly optimized anti-fMet antibody is a powerful, cost-effective tool for detecting fMet-bearing proteins across species. Furthermore, this approach provides a foundation for developing anti-pan-specific antibodies targeting other N-terminal modifications through acylation, alkylation, oxidation, arginylation, etc.
Authors
- Kyu‐Sang Park (ORCID: https://orcid.org/0000-0003-0322-9807)
- Cheol‐Sang Hwang (ORCID: https://orcid.org/0000-0002-0105-5957)
- Dasom Kim (ORCID: https://orcid.org/0000-0001-6389-0950)
Institutions
- Yonsei University (KR)
- Korea University (KR)
Publication Details
- Journal
- BioTechniques
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1080/07366205.2025.2467583
- Citations
- 3
- Primary Topic
- Peptidase Inhibition and Analysis
- Type
- article
- Field-Weighted Citation Impact
- 3.14
Funders
- Korea University