Ilani Tal, Fishburn C Simone, Levavi-Sivan Berta, Carmon Shari, Raveh Lily, Fuchs Sara
Department of Immunology, The Weizmann Institute of Science, Rehovot, Israel.
Cell Mol Neurobiol. 2002 Feb;22(1):47-56. doi: 10.1023/a:1015341712166.
D2 and D3 dopamine receptors belong to the superfamily of G protein-coupled receptors; they share a high degree of homology and are structurally similar. However, they differ from each other in their second messenger coupling properties. Previously, we have studied the differential coupling of these receptors to G proteins and found that while D2 receptor couples only to inhibitory G proteins, D3 receptor couples also to a stimulatory G protein, Gs. We aimed to investigate the molecular basis of these differences and to determine which domains in the receptor control its coupling to G proteins. For this purpose four chimeras were constructed, each composed of different segments of the original D2 and D3 receptors. We have demonstrated that chimeras with a third cytoplasmic loop of D2 receptor couple to Gi protein in a pattern characteristic of D2 receptor. On the other hand chimeras containing a third cytoplasmic loop of D3 receptor have coupling characteristics like those of D3 receptor, and they couple also to Gs protein. These findings demonstrate that the third cytoplasmic loop determines and accounts for the coupling of dopamine receptors D2 and D3 to G proteins.
D2和D3多巴胺受体属于G蛋白偶联受体超家族;它们具有高度的同源性且结构相似。然而,它们在第二信使偶联特性方面彼此不同。此前,我们研究了这些受体与G蛋白的差异偶联,发现虽然D2受体仅与抑制性G蛋白偶联,但D3受体还与刺激性G蛋白Gs偶联。我们旨在研究这些差异的分子基础,并确定受体中哪些结构域控制其与G蛋白的偶联。为此构建了四个嵌合体,每个嵌合体由原始D2和D3受体的不同片段组成。我们已经证明,具有D2受体第三胞质环的嵌合体以D2受体特有的模式与Gi蛋白偶联。另一方面,含有D3受体第三胞质环的嵌合体具有与D3受体相似的偶联特性,并且它们也与Gs蛋白偶联。这些发现表明,第三胞质环决定并解释了多巴胺受体D2和D3与G蛋白的偶联。