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Updated: Jun 20, 2026

Imaging Protein-protein Interactions in vivo
Published on: October 11, 2010
Expression cloning of the murine erythropoietin receptor
A D D'Andrea1, H F Lodish, G G Wong
1Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts 02142.
Abstract:
Two independent cDNA clones encoding the erythropoietin receptor (EPO-R) were isolated from a pXM expression library made from uninduced murine erythroleukemia (MEL) cells. The clones were identified by screening COS cell transfectants for binding and uptake of radioiodinated recombinant human erythropoietin. As inferred from the cDNA sequence, the murine erythropoietin receptor is a 507 amino acid polypeptide with a single membrane-spanning domain. It shows no similarities to known proteins or nucleic acid sequences in the data bases. Although the MEL cell EPO-R has a single affinity with a dissociation constant of approximately 240 pM, the EPO-R cDNA, expressed in COS cells, generates both a high-affinity (30 pM) and a low-affinity (210 pM) receptor.

