@article{APS9252,
author = {Ping LIU and Ming-zhu JIA and X Edward ZHOU and Parker W DE WAAL and Bradley M DICKSON and Bo LIU and Li HOU and Yan-ting YIN and Yan-yong KANG and Yi SHI and Karsten MELCHER and H Eric XU and Yi JIANG},
title = {The structural basis of the dominant negative phenotype of the Gα i1 β 1 γ 2 G203A/A326S heterotrimer},
journal = {Acta Pharmacologica Sinica},
volume = {37},
number = {9},
year = {2017},
keywords = {},
abstract = {Aim: Dominant negative mutant G proteins have provided critical insight into the mechanisms of G protein-coupled receptor (GPCR) signaling, but the mechanisms underlying the dominant negative characteristics are not completely understood. The aim of this study was to determine the structure of the dominant negative Gαi1β1γ2 G203A/A326S complex (Gi-DN) and to reveal the structural basis of the mutation-induced phenotype of Gαi1β1γ2.
Methods: The three subunits of the Gi-DN complex were co-expressed with a baculovirus expression system. The Gi-DN heterotrimer was purified, and the structure of its complex with GDP was determined through X-ray crystallography.
Results: The Gi-DN heterotrimer structure revealed a dual mechanism underlying the dominant negative characteristics. The mutations weakened the hydrogen bonding network between GDP/GTP and the binding pocket residues, and increased the interactions in the Gα-Gβγ interface. Concomitantly, the Gi-DN heterotrimer adopted a conformation, in which the C-terminus of Gαi and the N-termini of both the Gβ and Gγ subunits were more similar to the GPCR-bound state compared with the wild type complex. From these structural observations, two additional mutations (T48F and D272F) were designed that completely abolish the GDP binding of the Gi-DN heterotrimer.
Conclusion: Overall, the results suggest that the mutations impede guanine nucleotide binding and Gα-Gβγ protein dissociation and favor the formation of the G protein/GPCR complex, thus blocking signal propagation. In addition, the structure provides a rationale for the design of other mutations that cause dominant negative effects in the G protein, as exemplified by the T48F and D272F mutations.},
issn = {1745-7254}, url = {http://www.chinaphar.com/article/view/9252}
}