A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies

Abstract

SummaryEpitope tagging is a versatile approach to study different proteins using a well-defined and established methodology. To date, most epitope tags such as myc, HA, V5 and FLAG tags are recognized by antibodies which limits their application to fixed cells, tissues or protein samples. Here we introduce a broadly applicable tagging strategy utilizing a short peptide tag/chromobody (PepTag/PepCB) system. The addition of the small PepTag does not interfere with the examined structures in different cellular compartments and its detection with the fluorescently labeled Pep-chromobody (PepCB) enables optical antigen tracing in real time. By employing the phenomenon of antigen-mediated chromobody stabilization (AMCBS) using a turnover-accelerated PepCB we demonstrated that the system is suitable to visualize and quantify changes in Pep-tagged antigen concentration by quantitative live-cell imaging. We expect that this novel tagging strategy offers new opportunities to study the dynamic regulation of proteins, e.g. during cellular signaling, cell differentiation, or upon drug action.