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一种单克隆抗体消除制瘤素M的抗增殖活性。

Abrogation of the antiproliferative activity of oncostatin M by a monoclonal antibody.

作者信息

Radka S F, Naemura J R, Shoyab M

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, WA 98121.

出版信息

Cytokine. 1992 May;4(3):221-6. doi: 10.1016/1043-4666(92)90059-z.

Abstract

Oncostatin M (OM) is a novel cytokine which exhibits pleiotropic effects on a wide variety of normal and transformed cell lines. To determine some of the physiological functions of OM we have characterized several monoclonal antibodies to the recombinant molecule. Antibodies OM1 and OM2 bound native, but not denatured OM, suggesting they recognize non-contiguous epitopes. A third antibody, OM6, bound predominantly denatured OM. Of the two antibodies which detect discontinuous epitopes, OM2, but not OM1, was identified as a neutralizing antibody based on its ability to abrogate OM activity in the growth inhibition assay (GIA) and to inhibit OM binding in the radioreceptor assay (RRA). OM2 was equally effective in abrogating the functional effects of either natural or recombinant OM, thereby demonstrating that the active sites of these molecules are structurally similar, if not identical.

摘要

抑瘤素M(OM)是一种新型细胞因子,对多种正常细胞系和转化细胞系具有多效性作用。为了确定OM的一些生理功能,我们对重组分子的几种单克隆抗体进行了表征。抗体OM1和OM2能结合天然的而非变性的OM,这表明它们识别的是非连续表位。第三种抗体OM6主要结合变性的OM。在两种检测不连续表位的抗体中,基于其在生长抑制试验(GIA)中消除OM活性以及在放射受体试验(RRA)中抑制OM结合的能力,OM2而非OM1被鉴定为中和抗体。OM2在消除天然或重组OM的功能效应方面同样有效,从而表明这些分子的活性位点在结构上即使不相同也相似。

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