| Literature DB >> 9651882 |
K Lundstrom1, M P Turpin, C Large, G Robertson, P Thomas, X Q Lewell.
Abstract
Nine mutants and the wild-type human dopamine D3 receptor were expressed at high levels in BHK and CHO cells using the Semliki Forest virus system and were analysed for receptor binding with several structurally different dopamine D3 ligands. The mutation His349Leu showed a significant decrease in pKi values for raclopride, dopamine and GR218231, but an increase in affinity for GR99841. Thr369Val had an increase in pKi for both GR99841 and 7-OH-DPAT. The receptor modelling based on sequence alignment with bacteriorhodopsin indicated that Thr369 and His349 are located on the inside of the ligand binding pocket and the effect of the mutagenesis was therefore expected. The change in binding affinity for Thr369Val could be due to the location in the transmembrane domain VII close to the aspartate residue in domain III, the postulated counter ion for dopamine.Entities:
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Year: 1998 PMID： 9651882 DOI： 10.3109/10799899809047741
Source DB: PubMed Journal: J Recept Signal Transduct Res ISSN： 1079-9893 Impact factor: 2.092