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Second, although CODA-RET does not provide estimates of the degree of oligomerization, such as the affinity of the intermolecular interactions between GPCR subunits or the proportion of subunits forming oligomers, this technique does allow a qualitative measure of the ability of a specific endogenous or exogenous ligand to activate a GPCR homodimer or heterodimer and signal through a specific G protein ( 2 -like receptor ligands for D 4.4 R and D 4.7 R, but only when forming heteromers with D 2 R or 2A R ( Using CODA-RET, we found two possible mechanisms for the D 4.7 R gain of function as mediator of an inhibition of frontal cortico-striatal neurotransmission ( Figure 1 ): first, a specific increase in the potency of dopamine for the D 2 R-D 4.7 R, but not for D 2 R-D 4.4 R heteromer, as compared with the D 2 R homomer ( 2 R when it was forming D 2 R-D 4.4 R or D 2 R-D 4.7 R heteromers, respectively ( 4 R should not be expected to form heteromers, but homomers, which should be more prevalent with D 4.7 R than with D 4.4 R

doi: 10.1080/13697137.2018.1463982