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用于研究脱髓鞘性和感染性神经疾病中脑脊液和血清蛋白质的等电聚焦和等速电泳。

Isoelectric focusing and isotachophoresis for investigation of CSF and serum proteins in demyelinating and infectious neurological diseases.

作者信息

Kjellin K G, Siden A

出版信息

Adv Exp Med Biol. 1978;100:545-59. doi: 10.1007/978-1-4684-2514-7_40.

Abstract

Isoelectric focusing (IEF) and isotachophoresis (ITP), two methods with excellent separation capacities, have been adapted during recent years for the analysis of CSF proteins. The fractions separated by these techniques can be further studied by e.g. immunological methods. ITP has besides its high separation capacity several valuable advantages: very small samples are needed, unconcentrated CSF can be examined, the analyses are quickly performed and the results are immediately obtained on a recorder. Examinations by thin-layer IEF in a series of about 2,000 patients have afforded much new information about the CSF and serum proteins in many neurological diseases. Different complex CSF protein aberrations have been found in the gammaglobulin range as well as in more anodal positions in MS, infectious neurological diseases and Guillain-Barré syndromes. These aberrations are probably the result of several interacting factors, e.g. the temporal and spatial characteristics of the disease, the release of decomposition products from destroyed tissues, the genetically determined reactivity of the individual and the type of etiological agent.

摘要

等电聚焦(IEF)和等速电泳(ITP)是两种具有出色分离能力的方法,近年来已被应用于脑脊液蛋白质分析。通过这些技术分离出的组分可进一步通过例如免疫方法进行研究。ITP除了具有高分离能力外,还有几个宝贵的优点:所需样本量非常小,可以检测未浓缩的脑脊液,分析快速进行,结果可立即在记录仪上获得。对约2000例患者进行的薄层IEF检查提供了许多关于多种神经系统疾病中脑脊液和血清蛋白质的新信息。在多发性硬化症、感染性神经系统疾病和格林-巴利综合征中,在γ球蛋白范围内以及更向阳极位置发现了不同的复杂脑脊液蛋白质异常。这些异常可能是多种相互作用因素的结果,例如疾病的时间和空间特征、受损组织分解产物的释放、个体的遗传决定反应性以及病原体类型。

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