Analysis of epidermal growth factor receptor dimerization by BS3 cross-linking

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Abstract

Dimerization of receptor tyrosine kinases is a well-characterized process. It is imperative for the activation of many receptors, including the epidermal growth factor receptor (EGFR). EGFR has been shown to be regulated by a number of factors, including lipid raft localization. For example, alteration of the lipid raft localization of EGFR has been demonstrated to modify receptor dimerization. This protocol describes an assay to quantify EGFR dimers using BS3 cross-linking. BS3 cross-linking is well suited for this purpose because of its length, water solubility, and membrane impermeability. Although this protocol is written specifically for EGFR, the assay can be extrapolated in order to characterize dimerization of other receptor tyrosine kinases.

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Turk, H. F., & Chapkin, R. S. (2015). Analysis of epidermal growth factor receptor dimerization by BS3 cross-linking. Methods in Molecular Biology, 1233, 25–34. https://doi.org/10.1007/978-1-4939-1789-1_3

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