Delassalle A, Jacque C, Drouet J, Raoul M, Legrand J C, Cesselin F
Biochimie. 1980;62(2-3):159-65. doi: 10.1016/s0300-9084(80)80191-x.
The radioimmunoassay (RIA) for myelin basic protein (MBP) in biological fluids was reassessed in order to improve its sensitivity and eliminate some interferences. By using the preincubation technique and the charcoal-dextran-horse serum mixture for the separation step, the detection limit could be lowered to 200 pg/ml for cerebrospinal fluids (CSF), amniotic fluids (AF) and nervous tissue extracts and 600 pg/ml for sera. The RIA could be used directly on CSF, AF and nervous tissue extracts. Sera, however, had to be heated in citrate buffer at 100 degrees C in order to discard interfering material. The present method is 10 to 20 times more sensitive than others previously published. Moreover, it can be applied to amniotic fluid. The biological fluids had to be promptly frozen to avoid degradation of MBP.
为提高髓鞘碱性蛋白(MBP)生物体液放射免疫测定法(RIA)的灵敏度并消除一些干扰因素,对该方法进行了重新评估。通过采用预孵育技术以及在分离步骤中使用活性炭 - 葡聚糖 - 马血清混合物,脑脊液(CSF)、羊水(AF)和神经组织提取物的检测限可降至200 pg/ml,血清的检测限为600 pg/ml。该放射免疫测定法可直接用于脑脊液、羊水和神经组织提取物。然而,血清必须在柠檬酸盐缓冲液中于100℃加热,以去除干扰物质。本方法的灵敏度比先前发表的其他方法高10至20倍。此外,它可应用于羊水。生物体液必须迅速冷冻,以避免髓鞘碱性蛋白降解。