Anti-c-myc antibody 9E10: epitope key positions and variability characterized using peptide spot synthesis on cellulose

The 9E10 antibody epitope (EQKLISEEDL) derives from a protein sequence in the human proto-oncogen p62c-myc and is widely used as a protein fusion tag. This myc-tag is a powerful tool in protein localization, immunochemistry, ELISA or protein purification. Here, we characterize the myc-tag epitope by...

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Veröffentlicht in:Protein engineering 2001-10, Vol.14 (10), p.803-806
Hauptverfasser: Hilpert, K., Hansen, G., Wessner, H., Küttner, G., Welfle, K., Seifert, M., Höhne, W.
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Sprache:eng
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Zusammenfassung:The 9E10 antibody epitope (EQKLISEEDL) derives from a protein sequence in the human proto-oncogen p62c-myc and is widely used as a protein fusion tag. This myc-tag is a powerful tool in protein localization, immunochemistry, ELISA or protein purification. Here, we characterize the myc-tag epitope by substitutional analysis and length variation using peptide spot synthesis on cellulose. The key amino acids of this interaction are the core residues LISE. The shortest peptide with a strong binding signal is KLISEEDL. Dissociation constants of selected peptide variants to the antibody 9E10 were determined. scFv constructs with the shortest possible myc-tags were successfully detected by Western blot and ELISA, giving a signal comparable to that of the original myc-tag.
ISSN:0269-2139
1741-0126
1460-213X
1741-0134
DOI:10.1093/protein/14.10.803