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使用一种新型抗体检测血清中的前列腺特异性膜抗原。

Measurement of prostate-specific membrane antigen in the serum with a new antibody.

作者信息

Murphy G P, Tino W T, Holmes E H, Boynton A L, Erickson S J, Bowes V A, Barren R J, Tjoa B A, Misrock S L, Ragde H, Kenny G M

机构信息

Pacific Northwest Cancer Foundation, Cancer Research Division, Northwest Hospital, Seattle, Washington, USA.

出版信息

Prostate. 1996 Apr;28(4):266-71. doi: 10.1002/(SICI)1097-0045(199604)28:4<266::AID-PROS7>3.0.CO;2-B.

Abstract

Work to date has identified prostate-specific membrane antigen (PSMA) as a membrane-bound glycoprotein with high specificity for prostatic epithelial cells. PSMA reacts with the monoclonal antibody 7E11.C5, which is present in serum, seminal fluid, and prostatic epithelial cells, and is increased in its expression in the presence of a hormone refractory state associated with prostatic cancer. This report confirms these results and further documents the presence of the monoclonal antibody 3F5.4G6, which reacts with the extracellular domain of PSMA. This region of PSMA is also an element present in a truncated version of the protein, so-called PSM'. Immune precipitation with either 7E11.C5 or 3F5.4G6 yields an isolated protein species that are reactive with the reciprocal antibody in Western blot analysis. Thus, 3F5.4G6 recognizes the same PSMA protein as does 7E11.C5, but at different epitopes on essentially opposite ends of the molecule. These two antibodies are well suited for use in a sandwich immunoassay, either one as a capture or detection antibody. Current work on this is underway. This report also confirms that 7E11.C5 Western blots for PSMA are negative with normal human brain tissue. The monoclonal antibody 9H10 does not react with 3F5.4G6 or with 7E11.C5 in studies conducted herein. Moreover, 3F5.4G6 reacts with PSMA found in the LNCaP cell line, but not DU-145 or PC3, which lack PSMA.

摘要

迄今为止的研究已确定前列腺特异性膜抗原(PSMA)是一种对前列腺上皮细胞具有高度特异性的膜结合糖蛋白。PSMA与单克隆抗体7E11.C5发生反应,该抗体存在于血清、精液和前列腺上皮细胞中,并且在与前列腺癌相关的激素难治性状态下其表达会增加。本报告证实了这些结果,并进一步记录了单克隆抗体3F5.4G6的存在,该抗体与PSMA的细胞外结构域发生反应。PSMA的这一区域也是该蛋白截短版本(即所谓的“PSM”)中存在的一个元件。用7E11.C5或3F5.4G6进行免疫沉淀可产生一种分离的蛋白,该蛋白在蛋白质印迹分析中与相应抗体发生反应。因此,3F5.4G6与7E11.C5识别的是相同的PSMA蛋白,但识别的是分子基本相对两端的不同表位。这两种抗体非常适合用于夹心免疫测定,可任一种作为捕获抗体或检测抗体。目前正在对此开展研究工作。本报告还证实,用于PSMA的7E11.C5蛋白质印迹法检测正常人脑组织呈阴性。在本文进行的研究中,单克隆抗体9H10不与3F5.4G6或7E11.C5发生反应。此外,3F5.4G6与LNCaP细胞系中发现的PSMA发生反应,但不与缺乏PSMA的DU-145或PC3细胞系发生反应。

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