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The antigen recognized by the monoclonal antibody (mAb) MRC OX40 is present on activated rat CD4 positive T lymphocytes but not other cells. cDNA clones were isolated from an expression library using the MRC OX40 mAb and the protein sequence for the OX40 antigen deduced. It contains a typical signal sequence and a single putative transmembrane sequence of 25 predominantly hydrophobic amino acids giving an extracellular domain of 191 amino acids and a cytoplasmic domain of 36 amino acids. The sequence of the extracellular domain includes a cysteine-rich region with sequence similarities with the low affinity nerve growth factor receptor (NGFR) of neurons and the CD40 antigen present on human B cells. Within this region three cysteine-rich motifs can be recognized in OX40 compared with four similar motifs in both NGFR and CD40. OX40, CD40 and NGFR constitute a new superfamily of molecules with expression including lymphoid cells (OX40, CD40) and neuronal cells (NGFR). This is reminiscent of the immunoglobulin superfamily whose molecules are variously found at the surface of lymphoid or brain cells or both.

Type

Journal

EMBO J

Publication Date

04/1990

Volume

9

Pages

1063 - 1068

Keywords

Amino Acid Sequence, Animals, Antibodies, Monoclonal, Antigens, CD4, Antigens, Surface, Base Sequence, Cell Line, Cell Membrane, Cloning, Molecular, Gene Library, Laminin, Molecular Sequence Data, Nerve Growth Factors, Protein Conformation, Protein Sorting Signals, Rats, Rats, Inbred Strains, Receptors, Cell Surface, Receptors, Nerve Growth Factor, Sequence Homology, Nucleic Acid, T-Lymphocytes, Transfection