β 2-微球蛋白:方法及临床应用。

M D Poulik, P Gold, J Shuster
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引用次数: 24

摘要

2-微球蛋白是一种低分子量蛋白质,存在于大多数生物体液中。它最初是从镉中毒病人的尿液中分离出来的。建立了其氨基酸序列,并在结构上与免疫球蛋白恒定结构域相关。在抗β 2微球蛋白特异性抗体的帮助下,在所有有核细胞(正常和肿瘤细胞)的膜上检测到该蛋白。测量β 2微球蛋白的数量表明,在肾小管缺陷和其他一些病理条件包括肿瘤疾病的患者中存在高水平。在精液和初乳中检测到极高的水平。尽管与免疫球蛋白有结构上的关系,但使用特异性抗体检测β 2微球蛋白并没有证明与这些蛋白有免疫学上的关系。然而,这些抗体对所有表面携带β 2微球蛋白的细胞都有细胞毒性。发现β 2微球蛋白是人类和小鼠组织相容性抗原的一个组成部分,刺激了对该分子的进一步研究和兴趣。几组研究人员已经表明β 2微球蛋白是低分子量链,并与携带组织相容性抗原的高分子量链非共价结合。淋巴细胞组织相容性抗原(HLA)的结构已被免疫化学和生物学方法所证实,目前已被广泛接受。针对β 2微球蛋白的抗体在分离组织相容性抗原进行序列研究时非常有用。此外,β 2-微球蛋白抗体显示,β 2-微球蛋白可能与其他结构结合,如植物血凝素(PHA)受体、混合淋巴细胞培养(MLC)抗原等。小鼠胸腺白血病(TL)抗原也含有β 2-微球蛋白作为其结构的组成部分;其他肿瘤抗原可能具有类似的结构。通过这些研究,β 2-微球蛋白成为最著名的膜蛋白,可以作为研究细胞膜排列和功能的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
beta 2-Microglobulin: methods and clinical applications.

beta 2-Microglobulin is a low molecular weight protein that is found in most biological fluids. It was originally isolated from urine of cadmium-poisoned patients. Its amino acid sequence was established and shown to be structurally related to immunoglobulin constant domains. With the aid of antibodies specific against beta 2-microglobulin, the protein was detected on the membranes of all nucleated cells, normal and neoplastic. Measuring the quantity of beta 2-microglobulin showed that high levels are present in patients with renal tubular deficiencies and several other pathological conditions including neoplastic diseases. Extremely high levels were detected in seminal fluid and colostrum. Despite the structural relationship to immunoglobulins, no immunological relationship was demonstrated with these proteins using antibodies specific for beta 2-microglobulin. However, such antibodies are cytotoxic to all cells carrying beta 2-microglobulin on their surfaces. The discovery that beta 2-microglobulin is an integral part of the histocompatibility antigens of human and murine origin stimulated further research and interest in this molecule. Several groups of investigators have shown that beta 2-microglobulin is the low molecular weight chain and is noncovalently bound to a high molecular weight chain which carries the histocompatibility antigens. The structure of the histocompatibility antigens of lymphocytes (HLA) was shown by immunochemical as well as biological methods, and it is now well accepted. The antibodies against beta 2-microglobulin are extremely useful in the isolation of the histocompatibility antigens for sequence studies. Furthermore, the antibody to beta 2-microglobulin revealed that other structures may be bound to beta 2-microglobulin such as phytohemoagglutimin (PHA) receptors, mixed lymphocyte culture (MLC) antigens, etc. Murine thymus leukemia (TL) antigen also contains beta 2-microglobulin as an integral part of its structure; other tumor antigens may have a similar structure. Through all these studies, beta 2-microglobulin emerged as the best known membrane protein that can serve as a model for study of the arrangement and the function of the cell membrane.

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