Evaluation of the Dimerization Profiles of HER Tyrosine Kinases by Time-Resolved Förster Resonance Energy Transfer (TR-FRET) - Archive ouverte HAL
Article Dans Une Revue Methods in Molecular Biology Année : 2015

Evaluation of the Dimerization Profiles of HER Tyrosine Kinases by Time-Resolved Förster Resonance Energy Transfer (TR-FRET)

Résumé

Activation of receptor tyrosine kinases (RTK), such as those belonging to the human epidermal growth factor receptor (HER) family, occurs only after receptor dimerization, which is a crucial step for cellular signal transduction and diversification. The HER family includes four members (EGFR/HER1, HER2, HER3, and HER4) that can homodimerize or heterodimerize. Here, we describe immunoassays based on time-resolved Förster resonance energy transfer (TR-FRET) to profile EGFR-EGFR, HER2-HER2, and EGFR-HER2 dimers directly in tumor samples.

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Dates et versions

hal-02272233 , version 1 (05-11-2024)

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Evelyne Lopez-Crapez, Alexandre Ho-Pun-Cheung, Patrick Garnero, Hervé Bazin. Evaluation of the Dimerization Profiles of HER Tyrosine Kinases by Time-Resolved Förster Resonance Energy Transfer (TR-FRET). Methods in Molecular Biology, 2015, pp.45-55. ⟨10.1007/978-1-4939-1789-1_5⟩. ⟨hal-02272233⟩
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