Blatnik Matthew, Frizzell Norma, Thorpe Suzanne R, Baynes John W
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Diabetes. 2008 Jan;57(1):41-9. doi: 10.2337/db07-0838. Epub 2007 Oct 12.
(2-succinyl)cysteine (2SC) is formed by a Michael addition reaction of the Krebs cycle intermediate, fumarate, with cysteine residues in protein. We investigated the role of fumarate in chemical modification and inhibition of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), in vitro and in tissues of diabetic rats.
GAPDH was incubated with fumarate in PBS to assess effects of fumarate on enzyme activity in vitro. Sites of 2SC formation were determined by analysis of tryptic peptides by high-performance liquid chromatography-quadrupole/time-of-flight mass spectrometry. 2SC and fumarate in gastrocnemius muscle of control and streptozotocin-induced diabetic rats were measured by liquid chromatography/tandem mass spectrometry and by gas chromatography/mass spectrometry, respectively. GAPDH was isolated from muscle by immunoprecipitation, and sites of modification of GAPDH were determined by mass spectrometry analysis.
2SC was found, both in vitro and in vivo, about equally at active-site Cys-149 and nucleophilic Cys-244. Inactivation of GAPDH by fumarate in vitro correlated with formation of 2SC. In diabetic compared with control rats, fumarate and 2SC concentration increased approximately fivefold, accompanied by an approximately 25% decrease in GAPDH specific activity. The fractional modification of GAPDH by 2SC was significantly increased in diabetic versus control animals, consistent with the decreased specific activity of GAPDH in muscle of diabetic animals.
Fumarate contributes to inactivation of GAPDH in diabetes. 2SC may be a useful biomarker of mitochondrial stress in diabetes. Modification of GAPDH and other enzymes and proteins by fumarate may contribute to the metabolic changes underlying the development of diabetes complications.
(2-琥珀酰)半胱氨酸(2SC)是由三羧酸循环中间体富马酸与蛋白质中的半胱氨酸残基通过迈克尔加成反应形成的。我们研究了富马酸在体外以及糖尿病大鼠组织中对巯基酶甘油醛-3-磷酸脱氢酶(GAPDH)的化学修饰和抑制作用。
将GAPDH与富马酸在磷酸盐缓冲盐溶液(PBS)中孵育,以评估富马酸对体外酶活性的影响。通过高效液相色谱-四极杆/飞行时间质谱分析胰蛋白酶肽段来确定2SC的形成位点。分别采用液相色谱/串联质谱法和气相色谱/质谱法测定对照大鼠和链脲佐菌素诱导的糖尿病大鼠腓肠肌中的2SC和富马酸。通过免疫沉淀从肌肉中分离GAPDH,并通过质谱分析确定GAPDH的修饰位点。
在体外和体内均发现,活性位点的半胱氨酸-149和亲核性半胱氨酸-244处的2SC含量大致相同。富马酸在体外使GAPDH失活与2SC的形成相关。与对照大鼠相比,糖尿病大鼠体内富马酸和2SC浓度增加了约五倍,同时GAPDH的比活性降低了约25%。与对照动物相比,糖尿病动物中2SC对GAPDH的修饰分数显著增加,这与糖尿病动物肌肉中GAPDH比活性降低一致。
富马酸导致糖尿病中GAPDH失活。2SC可能是糖尿病中线粒体应激的有用生物标志物。富马酸对GAPDH和其他酶及蛋白质的修饰可能导致糖尿病并发症发生所潜在的代谢变化。