MICRO-TAG® is a cellular target engagement technology designed to quantify ligand–target interactions in native cellular environments. By converting target engagement into a measurable fluorescent signal, MICRO-TAG® enables reproducible, scalable and quantitative assays suitable for modern discovery workflows.

A short 15-amino acid peptide tag is fused to the protein of interest, which complements with a detection partner to form an active enzyme only when the target protein is properly folded and accessible. Ligand binding alters the thermal or kinetic stability of the target protein, modulating enzyme activity and producing a measurable fluorescence signal.
Assess ligand-induced stabilization or destabilization of target proteins across a temperature gradient to derive quantitative engagement metrics.
Monitor engagement dynamics over time to capture binding kinetics, residence effects, and mechanistic differences between compounds.
Measurements are performed in intact cells or lysates, preserving cellular context and avoiding artifacts common to biochemical-only assays.
Derive quantitative values such as Tagg₅₀ to enable objective comparison across compounds, targets, and experiments.
Standardized outputs allow reliable ranking of compound series and identification of weak or non-engaging hits early in discovery.
Consistent assay outputs enable comparison across projects, targets, and campaigns without assay reconfiguration.
The technology has been already verified compatible with commonly used real-time qPCR instruments such as QuantStudio (Thermo Fisher) and Cielo (Azure Biosystems).
MICRO-TAG® is patented under two patents: US12510537B2 and US20230204594A1. The first one covers the assembly and biochemistry of the MICRO-TAG system. The second one covers utility of the MICRO-TAG enzyme complementation in real time systems and its integration. Published: https://pubmed.ncbi.nlm.nih.gov/41285198/
MICRO-TAG® was developed and refined through extensive internal and collaborative discovery programs, including target validation, hit progression, and cellular DEL campaigns. Insights from these programs informed the standardization of the technology into reagent-based formats.
Measures cellular target engagement independent of target class or functional readout, enabling a unified assay framework across diverse single proteins and complexes.
Captures ligand-induced stabilization and destabilization in cells through temperature-series and real-time measurements, revealing binding dynamics beyond binary engagement.
Delivers standardized quantitative outputs using workflows compatible with common lab infrastructure, supporting cross-project comparability and program-scale deployment.
CellarisBio
San Diego, California, USA
Copyright © 2026 CellarisBio - All Rights Reserved.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.