Center for Medical Biochemistry, Max Perutz Labs, Vienna BioCenter, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Sci Signal. 2020 Jan 28;13(616):eaax9730. doi: 10.1126/scisignal.aax9730.
Epitope tags are short, linear antibody recognition sequences that enable detection of tagged fusion proteins by antibodies. Epitope tag position and neighboring sequences potentially affect its recognition by antibodies, and such context-dependent differences in tag binding may have a wide-ranging effect on data interpretation. We tested by Western blotting six antibodies that recognize the c-Myc epitope tag, including monoclonal antibodies 9E10, 4A6, 9B11, and 71D10 and polyclonal antibodies 9106 and A-14. All displayed context-dependent differences in their ability to detect N- or C-terminal Myc-tagged proteins. In particular, clone 9E10, the most cited Myc-tag antibody, displayed high context-dependent detection variability, whereas others, notably 4A6 and 9B11, showed much less context sensitivity in their detection of Myc-tagged proteins. The very high context sensitivity of 9E10 was further substantiated by peptide microarray analyses. We conclude that recently developed, purpose-made monoclonal antibodies specific for Myc have much more uniform reactivity in diverse assays and are much less context sensitive than is the legacy antibody 9E10.
表位标签是短的线性抗体识别序列,能够通过抗体检测标记融合蛋白。表位标签的位置和邻近序列可能会影响抗体对其的识别,并且这种标签结合的上下文相关差异可能会对数据解释产生广泛的影响。我们通过 Western blot 测试了六种识别 c-Myc 表位标签的抗体,包括单克隆抗体 9E10、4A6、9B11 和 71D10 以及多克隆抗体 9106 和 A-14。所有抗体在检测 N 端或 C 端 Myc 标记蛋白的能力上都表现出上下文相关的差异。特别是,被引用最多的 Myc 标签抗体克隆 9E10 显示出很高的上下文依赖性检测变异性,而其他抗体,特别是 4A6 和 9B11,在检测 Myc 标记蛋白时表现出较小的上下文敏感性。9E10 的非常高的上下文敏感性还通过肽微阵列分析得到了进一步证实。我们得出结论,最近开发的、专门针对 Myc 的单克隆抗体在各种检测中具有更一致的反应性,并且比传统抗体 9E10 的上下文敏感性低得多。