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制备抗粘蛋白多肽抗血清以研究粘蛋白生物合成。

Preparation of anti-mucin polypeptide antisera to study mucin biosynthesis.

作者信息

Tytgat K M, Klomp L W, Bovelander F J, Opdam F J, Van der Wurff A, Einerhand A W, Büller H A, Strous G J, Dekker J

机构信息

Laboratory for Pediatric Gastroenterology and Nutrition, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Anal Biochem. 1995 Apr 10;226(2):331-41. doi: 10.1006/abio.1995.1233.

Abstract

Mucins are very heavily O-glycosylated glycoproteins. For in depth studies on the cell biological aspects of mucins, anti-polypeptide antibodies are essential. We therefore developed a method for the preparation and screening of polyclonal antisera against mucin peptide epitopes. Mucins from five different tissues were isolated using CsCl/guanidinium.HCl density gradient centrifugation, and polyclonal antisera were prepared. Specificity for mucin peptide epitopes was determined by Western blotting, immunohistochemistry, and immunoprecipitation. The versatility of each anti-mucin antiserum for the study of mucin biosynthesis was tested in metabolic labeling experiments on tissue explants. All polyclonal antisera were directed primarily against peptide epitopes of mucin precursors as well as of fully glycosylated mucins. Each of the polyclonal antisera enabled us to study the mucin biosynthesis in the organ where the mucin was isolated from originally. Our mucin isolation method yields very pure mucins with sufficiently intact polypeptides to reproducibly elicit polyclonal anti-polypeptide antisera. As the sera recognized the polypeptides, primarily independent of the state of O-glycosylation, the intermediate steps in the biosynthesis of the mucins could be identified.

摘要

黏蛋白是高度O-糖基化的糖蛋白。对于深入研究黏蛋白的细胞生物学方面,抗多肽抗体至关重要。因此,我们开发了一种制备和筛选针对黏蛋白肽表位的多克隆抗血清的方法。使用CsCl/盐酸胍密度梯度离心法从五种不同组织中分离出黏蛋白,并制备了多克隆抗血清。通过蛋白质印迹法、免疫组织化学和免疫沉淀法确定对黏蛋白肽表位的特异性。在组织外植体的代谢标记实验中测试了每种抗黏蛋白抗血清用于研究黏蛋白生物合成的通用性。所有多克隆抗血清主要针对黏蛋白前体以及完全糖基化黏蛋白的肽表位。每种多克隆抗血清都使我们能够研究最初从中分离出黏蛋白的器官中的黏蛋白生物合成。我们的黏蛋白分离方法可产生非常纯的黏蛋白,其多肽足够完整,能够可重复地引发多克隆抗多肽抗血清。由于这些血清识别多肽,主要独立于O-糖基化状态,因此可以鉴定黏蛋白生物合成的中间步骤。

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