Groome N P, Dawkes A, Gales M, Hruby S, Alvord E C
J Neuroimmunol. 1986 Oct;12(4):253-64. doi: 10.1016/0165-5728(86)90032-9.
Three monoclonal antibodies reactive with human myelin basic protein have been used to develop immunoradiometric assays for this protein. Clone 1, a mouse IgG2a, is reactive with an epitope in the region 129-138. Clone 2, a mouse IgG1, is reactive with the region 119-131. Clone 12, a rat IgG, is reactive with the region 86-96. Competition experiments show that the reactions of Clone 1 and Clone 2 are mutually exclusive, probably because of steric effects. In contrast, when either Clone 1 or Clone 2 react they cause minimal interference with the subsequent binding of Clone 12. Less than 1 ng/ml of myelin basic protein can be detected in each of the two immunoradiometric assays developed. Clone 12 can also be used on its own in a competitive immunoassay to detect around 2 ng/ml. Using an extraction technique before the assay, serum or plasma can also be investigated. Assays for defined regions of myelin basic protein should prove valuable in identifying the products of myelin catabolism in patients with demyelinating disease.
三种与人髓鞘碱性蛋白反应的单克隆抗体已被用于开发针对该蛋白的免疫放射分析方法。克隆1是一种小鼠IgG2a,与129 - 138区域的一个表位反应。克隆2是一种小鼠IgG1,与119 - 131区域反应。克隆12是一种大鼠IgG,与86 - 96区域反应。竞争实验表明,克隆1和克隆2的反应相互排斥,可能是由于空间效应。相比之下,当克隆1或克隆2反应时,它们对随后克隆12的结合造成的干扰最小。在开发的两种免疫放射分析方法中,每种方法都能检测到低于1 ng/ml的髓鞘碱性蛋白。克隆12也可单独用于竞争性免疫分析,以检测约2 ng/ml的蛋白。在检测前使用提取技术,也可以对血清或血浆进行检测。针对髓鞘碱性蛋白特定区域的分析方法在识别脱髓鞘疾病患者髓鞘分解代谢产物方面应具有重要价值。