Friedman Erin J, Temple Brenda R S, Hicks Stephanie N, Sondek John, Jones Corbin D, Jones Alan M
Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
J Mol Biol. 2009 Oct 2;392(4):1044-54. doi: 10.1016/j.jmb.2009.07.076. Epub 2009 Jul 30.
Gbeta subunits from heterotrimeric G-proteins (guanine nucleotide-binding proteins) directly bind diverse proteins, including effectors and regulators, to modulate a wide array of signaling cascades. These numerous interactions constrained the evolution of the molecular surface of Gbeta. Although mammals contain five Gbeta genes comprising two classes (Gbeta1-like and Gbeta5-like), plants and fungi have a single ortholog, and organisms such as Caenorhabditis elegans and Drosophila melanogaster contain one copy from each class. A limited number of crystal structures of complexes containing Gbeta subunits and complementary biochemical data highlight specific sites within Gbetas needed for protein interactions. It is difficult to determine from these interaction sites what, if any, additional regions of the Gbeta molecular surface comprise interaction interfaces essential to Gbeta's role as a nexus in numerous signaling cascades. We used a comparative evolutionary approach to identify five known and eight previously unknown putative interfaces on the surface of Gbeta. We show that one such novel interface occurs between Gbeta and phospholipase C beta2 (PLC-beta2), a mammalian Gbeta interacting protein. Substitutions of residues within this Gbeta-PLC-beta2 interface reduce the activation of PLC-beta2 by Gbeta1, confirming that our de novo comparative evolutionary approach predicts previously unknown Gbeta-protein interfaces. Similarly, we hypothesize that the seven remaining untested novel regions contribute to putative interfaces for other Gbeta interacting proteins. Finally, this comparative evolutionary approach is suitable for application to any protein involved in a significant number of protein-protein interactions.
异源三聚体G蛋白(鸟嘌呤核苷酸结合蛋白)的Gβ亚基直接与多种蛋白质结合,包括效应器和调节剂,以调节一系列信号级联反应。这些众多的相互作用限制了Gβ分子表面的进化。虽然哺乳动物含有五个Gβ基因,分为两类(Gβ1样和Gβ5样),但植物和真菌只有一个直系同源物,而秀丽隐杆线虫和黑腹果蝇等生物则从每类中各含有一个拷贝。有限数量的包含Gβ亚基的复合物晶体结构和补充的生化数据突出了Gβ中蛋白质相互作用所需的特定位点。从这些相互作用位点很难确定Gβ分子表面的哪些额外区域(如果有的话)构成了Gβ作为众多信号级联反应中的连接点所必需的相互作用界面。我们使用比较进化方法来识别Gβ表面上五个已知的和八个以前未知的假定界面。我们表明,这样一个新界面出现在Gβ和磷脂酶Cβ2(PLC-β2)之间,PLC-β2是一种与哺乳动物Gβ相互作用的蛋白质。该Gβ-PLC-β2界面内残基的替换降低了Gβ1对PLC-β2的激活,证实了我们的从头比较进化方法预测了以前未知的Gβ-蛋白质界面。同样,我们假设其余七个未经测试的新区域有助于其他与Gβ相互作用的蛋白质的假定界面。最后,这种比较进化方法适用于任何参与大量蛋白质-蛋白质相互作用的蛋白质。