Vadas P, Stefanski E, Pruzanski W
Inflammation. 1986 Jun;10(2):183-93. doi: 10.1007/BF00916000.
The influence of plasma proteins on quantitation of the proinflammatory enzyme phospholipase A2 (PLA2) from rheumatoid synovial fluid was studied using two different assays. Human and bovine serum albumins increased the rate of PLA2 hydrolysis of membrane-associated phospholipid substrates. In contrast, albumin profoundly inhibited the PLA2 hydrolysis of synthetic phospholipids in micellar dispersion. Other plasma proteins (alpha, beta and gamma-globulins) had minimal effect on PLA2 activity in either assay system. Since the presence of albumin may compromise estimation of PLA2 and of phospholipase-inhibitory proteins, the appropriate selection of assay conditions is obligatory for the accurate quantitation of their respective activities.
使用两种不同的检测方法研究了血浆蛋白对类风湿性滑液中促炎酶磷脂酶A2(PLA2)定量的影响。人血清白蛋白和牛血清白蛋白提高了膜相关磷脂底物的PLA2水解速率。相比之下,白蛋白在胶束分散体中显著抑制了合成磷脂的PLA2水解。在任一检测系统中,其他血浆蛋白(α、β和γ球蛋白)对PLA2活性的影响最小。由于白蛋白的存在可能会影响PLA2和磷脂酶抑制蛋白的估计,因此,为准确测定它们各自的活性,必须适当选择检测条件。