Gα_q allosterically activates and relieves autoinhibition of p63RhoGEF

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• 作者：Aruna Shankaranarayanan ; Cass ; ra A. Boguth ; Susanne Lutz ; Christiane Vettel ; Franca Uhlemann ; Mohamed Aittaleb ; Thomas Wiel ; John J.G. Tesmer
• 关键词：Gα ; _q ; p63RhoGEF ; RhoA ; Dbl homology domain ; Pleckstrin homology domain ; Autoinhibition ; Allosteric activation
• 刊名：Cellular Signalling
• 出版年：2010
• 出版时间：July 2010
• 年：2010
• 卷：22
• 期：7
• 页码：1114-1123
• 全文大小：2722 K

文摘

Gα_q directly activates p63RhoGEF and closely related catalytic domains found in Trio and Kalirin, thereby linking G_q-coupled receptors to the activation of RhoA. Although the crystal structure of Gα_q in complex with the catalytic domains of p63RhoGEF is available, the molecular mechanism of activation has not yet been defined. In this study, we show that membrane translocation does not appear to play a role in Gα_q-mediated activation of p63RhoGEF, as it does in some other RhoGEFs. Gα_q instead must act allosterically. We next identify specific structural elements in the PH domain that inhibit basal nucleotide exchange activity, and provide evidence that Gα_q overcomes this inhibition by altering the conformation of the α6–αN linker that joins the DH and PH domains, a region that forms direct contacts with RhoA. We also identify residues in Gα_q that are important for the activation of p63RhoGEF and that contribute to Gα subfamily selectivity, including a critical residue in the Gα_q C-terminal helix, and demonstrate the importance of these residues for RhoA activation in living cells.