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

被引:53
作者
Hilpert, K
Hansen, G
Wessner, H
Küttner, G
Welfle, K
Seifert, M
Höhne, W
机构
[1] Humboldt Univ, Univ Klinikum Charite, Inst Biochem, D-10117 Berlin, Germany
[2] Max Delbruck Ctr Mol Med, D-13122 Berlin, Germany
[3] Humboldt Univ, Univ Klinikum Charite, Inst Med Immunol, D-10117 Berlin, Germany
来源
PROTEIN ENGINEERING | 2001年 / 14卷 / 10期
关键词
epitope characterization; MAB; 9E10; myc-tag; peptide spot synthesis; substitutional analysis;
D O I
10.1093/protein/14.10.803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:803 / 806
页数:4
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