Vensel L A, Kantrowitz E R
J Biol Chem. 1980 Aug 10;255(15):7306-10.
Reaction of phenylglyoxal, a reagent specific for arginine residues, with porcine phospholipiase A2 results in complete elimination of catalytic activity. The modification reaction is markedly dependent on pH. Other dicarbonyl compounds such as 2,3-butanedione and 1,2-cyclohexanedione also react with the enzyme to cause loss of activity but at significantly slower rates. At pH 7.0, the inactivation can be slightly retarded in the presence of Ca2+ and almost completely prevented in the presence of n-alkylphosphorylchline inhibitors. At pH 8.5, the n-alkylphosphorylcholine inhibitors are less effective. The decrease in enzymatic activity correlates with the modification of about 1 arginine residue/phospholipase A2 molecule. The data suggest that the arginine is involved in the binding of the phosphate portion of the substrate to the enzyme.
苯乙二醛(一种对精氨酸残基具有特异性的试剂)与猪磷脂酶A2反应会导致催化活性完全丧失。修饰反应明显依赖于pH值。其他二羰基化合物,如2,3-丁二酮和1,2-环己二酮,也会与该酶反应导致活性丧失,但速率明显较慢。在pH 7.0时,Ca2+的存在可使失活略有延迟,而在正烷基磷酰胆碱抑制剂存在时几乎可完全防止失活。在pH 8.5时,正烷基磷酰胆碱抑制剂的效果较差。酶活性的降低与大约每分子磷脂酶A2修饰1个精氨酸残基相关。数据表明,精氨酸参与底物磷酸部分与酶的结合。