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.

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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

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article

Development of an enhanced anti-pan-N-formylmethionine-specific antibody

Kyu‐Sang Park, Cheol‐Sang Hwang, Dasom Kim
3 citations
BioTechniques
Peptidase Inhibition and Analysis
3.14
article

Development of an enhanced anti-pan-N-formylmethionine-specific antibody

Kyu‐Sang Park, Cheol‐Sang Hwang, Dasom Kim
article en
3 citations

Abstract

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.

BioTechniquesVol. 77(2)
Yonsei University (KR), Korea University (KR)
Korea University
Openalex Percentile: Top 9%
Peptidase Inhibition and Analysis
3.14
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