We have synthesised the beta 1-subunit of the bovine GABA, receptor in
stable, continuous insect (Spodoptera frugiperda) cell lines. A cDNA
was integrated randomly into the insect cell genome under control of a
baculovirus immediate early (IE-1) gene promoter. Transformed cells w
ere obtained by co-transfection of the insect cells with pIEK1.GR beta
1, encoding the beta 1 subunit cDNA, and pIEK1.neo, encoding the neom
ycin resistance gene. G-418-resistant clones were selected and expande
d into continuous cell lines synthesising functional, GABA-gated, homo
-oligomeric chloride channels. These cell lines had significant advant
ages over the transient baculovirus expression system for the characte
risation of receptors using electrophysiological recording techniques.