提高人和鼠 β2-微球蛋白多克隆抗体的特异性,以替代免疫分析中使用的单克隆抗体

N. Karkischenko, V. Ezerskiy, O. B. Zhukova, E. Koloskova, N. V. Petrova
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引用次数: 0

摘要

高特异性试剂,即蛋白质及其抗体,是验证转基因/基因敲除动物生物模型有效性系统的必要组成部分。特别是,俄罗斯 FMBA 生物医学技术科学中心近年来创建的几种 HLA 系转基因小鼠和 β2m 基因敲除小鼠的器官和组织蛋白质部分中小鼠和人类 β2-微球蛋白的鉴定是其认证的最重要阶段。在研究的第一阶段,我们获得了重组小鼠和人β2-微球蛋白(mβ2mg 和 hβ2mg)的大肠杆菌菌株,并分离和纯化了蛋白质。下一阶段的工作是获得固定了 mβ2mg 和 hβ2mg 的亲和吸附剂。为了提高血清的物种特异性,"兔抗-hβ2mg "被去除了重组蛋白 mβ2mg,反之,"兔抗-mβ2mg "被去除了重组蛋白 hβ2mg。 利用亲和吸附剂从去除了的血清中纯化出了高特异性抗体。使用点印迹法和西式印迹法,以耗竭和亲和纯化的兔抗 hβ2mg 抗体为例,结果表明它们相对于 hβ2mg 的特异性显著提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increasing, the Specificity of Polyclonal Antibodies to Human and Mouse β2-Microglobulin as an Alternative to the Use of Monoclonal Antibodies in Immunological Analysis
Highly specific reagents, i.e., proteins and antibodies to them, are the necessary components of systems for verifying the effectiveness of transgenic/knockout animal biomodels. In particular, the identification of   mouse and human β2-microglobulin in the protein fractions of organs and tissues of transgenic and β2m knockout mice of several HLA lines, which have been created in recent years at the Scientific Center of  Biomedical Technologies of the FMBA of Russia, is the most important stage of their certification. At  the first stage of our research,  E. coli  producing strains of recombinant mouse and human β2-microglobulin (mβ2mg and hβ2mg) were obtained, the proteins were isolated and purified. At the next stage of the work, affine sorbents with immobilized mβ2mg and hβ2mg were obtained. To increase the species specificity of the serum, “rabbit-anti-hβ2mg” were depleted against the recombinant protein mβ2mg, and, conversely, “rabbit-anti-mβ2mg” were depleted against the recombinant protein hβ2mg. Highly specific antibodies were purified from depleted sera using affinity sorbents. Using dot- and western-blotting methods оn the example of depleted and affinity-purified rabbit-anti-hβ2mg antibodies, a significant increase in  their specificity relative to hβ2mg was shown.
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