Deorphanization of the human leukocyte tyrosine kinase (LTK) receptor by a signaling screen of the extracellular proteome

Proc Natl Acad Sci U S A. 2014 Nov 4;111(44):15741-5. doi: 10.1073/pnas.1412009111. Epub 2014 Oct 20.

Abstract

There are many transmembrane receptor-like proteins whose ligands have not been identified. A strategy for finding ligands when little is known about their tissue source is to screen each extracellular protein individually expressed in an array format by using a sensitive functional readout. Taking this approach, we have screened a large collection (3,191 proteins) of extracellular proteins for their ability to activate signaling of an orphan receptor, leukocyte tyrosine kinase (LTK). Only two related secreted factors, FAM150A and FAM150B (family with sequence similarity 150 member A and member B), stimulated LTK phosphorylation. FAM150A binds LTK extracellular domain with high affinity (K(D) = 28 pM). FAM150A stimulates LTK phosphorylation in a ligand-dependent manner. This strategy provides an efficient approach for identifying functional ligands for other orphan receptors.

Keywords: FAM150A; extracellular protein; leukocyte tyrosine kinase; library screening; orphan receptor.

MeSH terms

  • Cytokines / genetics
  • Cytokines / metabolism*
  • Female
  • HEK293 Cells
  • Humans
  • Male
  • Phosphorylation / physiology
  • Protein Binding / physiology
  • Protein Structure, Tertiary
  • Proteome / genetics
  • Proteome / metabolism*
  • Proteomics
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Signal Transduction / physiology*

Substances

  • ALKAL1 protein, human
  • ALKAL2 protein, human
  • Cytokines
  • Proteome
  • LTK protein, human
  • Receptor Protein-Tyrosine Kinases