Distal switch II region of Ras2p is required for interaction with guanine nucleotide exchange factor

被引:19
作者
Crechet, JB
Bernardi, A
Parmeggiani, A
机构
[1] ECOLE POLYTECH,GRP BIOPHYS EQUIPE 2,F-91128 PALAISEAU,FRANCE
[2] CNRS,ENZYMOL LAB,F-91198 GIF SUR YVETTE,FRANCE
[3] UNIV PARIS 07,INST JACQUES MONOD,F-75251 PARIS,FRANCE
关键词
D O I
10.1074/jbc.271.29.17234
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interaction of Saccharomyces cerevisiae Ras2p with the catalytic domain of the GDP/GTP exchange factors (GEFs) mouse CDC25(Mm), yeast Cdc25p, and Sdc25p was analyzed by introducing the substitution R80D/N81D into Ras2p S24N, a mutant that is shown to interfere with the Ras2p wild type (wt)-GEF interaction by forming a stable complex. The triple mutant, Like Ras2p R80D/N81D, did not interfere with the action of GEF on Ras2p wt (or H-Ras p21) and was unable to form a stable complex with GEF. The GEF stimulation of the nucleotide dissociation of the triple mutant was virtually abolished and strongly decreased with the double mutant. The affinity of Ras2p S24N/R80D/N81D for GDP and GTP was decreased 3 and 4 orders of magnitude, respectively, hire that of Ras2p S24N, whereas the double mutant behaved as Ras2p wt. Like Ras2p S24N and unlike Ras2p R80D/N81D, the GTP-bound triple mutant did not activate adenylyl cyclase. Thus, the triple mutant and Ras2p S24N have opposite properties toward the binding to GEF but similarly modified behaviors toward GDP, GTP, and adenylyl cyclase. This work emphasizes the determinant role of the distal switch II region of Ras2p for the interaction with GEF and the different structural background of the interaction with adenylyl cyclase.
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页码:17234 / 17240
页数:7
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