| Literature DB >> 8139691 |
T D Bartley1, R W Hunt, A A Welcher, W J Boyle, V P Parker, R A Lindberg, H S Lu, A M Colombero, R L Elliott, B A Guthrie.
Abstract
A protein ligand for the ECK receptor protein-tyrosine kinase has been isolated by using the extracellular domain (ECK-X) of the receptor as an affinity reagent. Initially, concentrated cell culture supernatants were screened for receptor binding activity using immobilized ECK-X in a surface plasmon resonance detection system. Subsequently, supernatants from selected cell lines were fractionated directly by receptor affinity chromatography, resulting in the single-step purification of B61, a protein previously identified as the product of an early response gene induced by tumour necrosis factor-alpha. We report here that recombinant B61 induces autophosphorylation of ECK in intact cells, consistent with B61 being an authentic ligand for ECK. ECK is a member of a large orphan receptor protein-tyrosine kinase family headed by EPH, and we suggest that ligands for other members of this family will be related to B61, and can be isolated in the same way.Entities:
Mesh:
Substances:
Year: 1994 PMID: 8139691 DOI: 10.1038/368558a0
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962