Molecular characterization of the human neuropeptide YY2-receptor

Five neuropeptide Y receptors, the Y-1-, Y-2-, Y-4-, Y-5- and y(6)-subtypes , have been cloned, which belong to the rhodopsin-like G-protein-coupled, 7 -transmembrane helix-spanning receptors and bind the 36-mer neuromodulator NPY (neuropeptide Y) with nanomolar affinity. In this study, the Y-2-recept or subtype expressed in a human neuroblastoma cell line (SMS-KAN) and in tr ansfected Chinese hamster ovary cells (CHO-hY2) was characterized on the pr otein level by using photoaffinity labeling and antireceptor antibodies. Tw o photoactivatable analogues of NPY were synthesized, in which a Tyr residu e was substituted by the photoreactive amino acid 4-(3-trifluoromethyl)-3H- diazirin-3-ylphenylalanine ((Tmd)Phe), [N-alpha-biotinyl-Ahx(2),(Tmd)Phe(36 )]NPY (Tmd36), and the Y-2-receptor subtype selective [N-alpha-biotinyl-Ahx (2),Ahx(5-24),(Tmd)Phe(27)]NPY (Tmd27). Both analogues were labeled with [H -3]succinimidylpropionate at Lys(4) and bind to the Y-2-receptor with affin ity similar to that of the native ligand. A synthetic fragment of the secon d (E2) extracellular loop was used to generate subtype selective antirecept or antibodies against the Y-2-receptor. Photoaffinity labeling of the recep tor followed by SDS-PAGE and detection of bound radioactivity and SDS-PAGE of solubilized receptors and subsequent Western blotting revealed the same molecular masses. Two proteins correspondingly have been detected for each cell line with molecular masses of 58 +/- 4 and 50 +/- 4 kDa, respectively.