Expression and characterization of the rat D3 dopamine receptor: pharmacologic properties and development of antibodies.

TitleExpression and characterization of the rat D3 dopamine receptor: pharmacologic properties and development of antibodies.
Publication TypeJournal Article
Year of Publication1993
AuthorsBoundy VA, Luedtke RR, Gallitano AL, Smith JE, Filtz TM, Kallen RG, Molinoff PB
JournalJ Pharmacol Exp Ther
Volume264
Issue2
Pagination1002-11
Date Published1993 Feb
ISSN0022-3565
KeywordsAmino Acid Sequence, Animals, Baculoviridae, Binding Sites, Cells, Cultured, Female, Humans, Immune Sera, Molecular Sequence Data, Moths, Precipitin Tests, Rabbits, Rats, Receptors, Dopamine, Receptors, Dopamine D2, Receptors, Dopamine D3, Recombinant Proteins, RNA, Messenger, Salicylamides
Abstract

A baculovirus expression system provided an enriched source of biologically and immunologically active D3 dopamine receptors. Receptors expressed in Spodoptera frugiperda insect (Sf9) cells at a density of 5 to 15 pmol/mg of protein displayed high affinity for the antagonists, eticlopride, fluphenazine and spiroperidol, and the agonist, N-propylnorapomorphine. The binding of agonists was not sensitive to GTP. Antisera raised against synthetic peptides in the third intracellular loop of the D3 dopamine receptor immunoprecipitated binding sites for (S)-3-[125I]-iodo-2-hydroxy-5,6-dimethoxy-N-[(1-ethyl-2-pyrrolidinyl)- methyl]-benzamide from solubilized extracts of infected Sf9 cells and detergent extracts of rat caudate. These antisera specifically recognized a single band on immunoblots of Sf9 cells infected with recombinant D3 baculovirus. Both the immunoprecipitation and immunoblot reactions were blocked by preincubation of the antisera with the immunization peptide. These results suggest that the D3 receptor protein is expressed in rat brain.

Alternate JournalJ. Pharmacol. Exp. Ther.
PubMed ID8437101
Grant ListF30 MH010161 / MH / NIMH NIH HHS / United States
MH10161 / MH / NIMH NIH HHS / United States
MH14654 / MH / NIMH NIH HHS / United States
NS18591 / NS / NINDS NIH HHS / United States