3.8 Article

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

Journal

PROTEIN ENGINEERING
Volume 14, Issue 10, Pages 803-806

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/protein/14.10.803

Keywords

epitope characterization; MAB 9E10; myc-tag; peptide spot synthesis; substitutional analysis

Ask authors/readers for more resources

The 9E10 antibody epitope (EQKLISEEDL) derives from a protein sequence in the human proto-oncogen p62(c-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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available