Milligan G
Department of Biochemistry, University of Glasgow, Scotland.
Cell Signal. 1989;1(1):65-74. doi: 10.1016/0898-6568(89)90021-1.
The major G-protein of rat glioma C6BU1 cells corresponds immunologically to Gi2. In the absence of guanine nucleotides, this protein is shown to be a substrate for ADP-ribosylation catalysed by both cholera and pertussis toxins. Under these conditions, a receptor for a growth factor, which has previously been shown to be activated by foetal calf serum, modulated the effects of both cholera and pertussis toxins on the G-protein. These ligand-mediated alterations of cholera and pertussis toxin-catalysed ADP ribosylation demonstrate that, in this system, the growth factor receptor interacts functionally with Gi2.