Glutathiolated Ras: Characterization and implications for Ras activation

• Published in: Free radical biology & medicine Vol. 57; pp. 221 - 229
• Main Authors: Hobbs, G. Aaron, Bonini, Marcelo G., Gunawardena, Harsha P., Chen, Xian, Campbell, Sharon L.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.04.2013
• Subjects: apoptosis; autoxidation; binding properties; cell growth; cysteine; dissociation; Enzyme Activation; Free radicals; Glutathione; Glutathione - chemistry; Glutathione - metabolism; Guanosine Diphosphate - chemistry; Guanosine Diphosphate - metabolism; guanosine triphosphate; Guanosine Triphosphate - chemistry; Guanosine Triphosphate - metabolism; guanosinetriphosphatase; Humans; hydrolysis; mass spectrometry; nitric oxide; Nitric Oxide - chemistry; nitrogen dioxide; Nitrogen Dioxide - metabolism; nuclear magnetic resonance spectroscopy; Nuclear Magnetic Resonance, Biomolecular; Oxidation; Oxidative cysteine modifications; Ras GTPases; ras Guanine Nucleotide Exchange Factors - metabolism; ras Proteins - metabolism; Reactive oxygen and nitrogen species; Reactive Oxygen Species - metabolism; regulatory proteins; eNOS; BAEC; Free radicals; MS; DAF; HCD; GEF; RasSNO; NO2; SOS; SIM; Reactive oxygen and nitrogen species; GAP; ROS; Ras GTPases; RasSSG; Oxidation; VSMC; HSQC; Oxidative cysteine modifications; MANT-GDP; DEANO; Glutathione
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2012.10.531

Ras GTPases cycle between active GTP-bound and inactive GDP-bound forms to regulate a multitude of cellular processes, including cell growth, differentiation, and apoptosis. The activation state of Ras is regulated by protein modulatory agents that accelerate the slow intrinsic rates of GDP dissociation and GTP hydrolysis. Similar to the action of guanine-nucleotide exchange factors, the rate of GDP dissociation can be greatly enhanced by the reaction of Ras with small-molecule redox agents, such as nitrogen dioxide, which can promote Ras activation. Nitrogen dioxide is an autoxidation product of nitric oxide and can react with an accessible cysteine of Ras to cause oxidation of the bound guanine nucleotide to facilitate Ras guanine nucleotide dissociation. Glutathione has also been reported to modify Ras and alter its activity. To elucidate the mechanism by which glutathione alters Ras guanine nucleotide binding properties, we performed NMR, top-down and bottom-up mass spectrometry, and biochemical analyses of glutathiolated Ras. We determined that treatment of H-Ras, lacking the nonconserved hypervariable region, with oxidized glutathione results in glutathiolation specifically at cysteine 118. However, glutathiolation does not alter Ras structure or biochemical properties. Rather, changes in guanine nucleotide binding properties and Ras activity occur upon exposure of Ras to free radicals, presumably through the generation of a cysteine 118 thiyl radical. Interestingly, Ras glutathiolation protects Ras from further free radical-mediated activation events. Therefore, glutathiolation does not affect Ras activity unless Ras is modified by glutathione through a radical-mediated mechanism. ► Ras is selectively modified by glutathione at cysteine 118. ► Ras structure is unaffected by glutathione modification at cysteine 118. ► Ras glutathiolation is nonactivating unless it proceeds through a free radical. ► Nucleotide exchange and hydrolysis of glutathiolated Ras are similar to those of wild-type Ras. ► Free radical-induced modifications at cysteine 118 activate Ras.