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用单克隆抗体从人肺成纤维细胞质膜中鉴定出一种64 kDa硫酸乙酰肝素蛋白聚糖核心蛋白。

Identification of a 64 kDa heparan sulphate proteoglycan core protein from human lung fibroblast plasma membranes with a monoclonal antibody.

作者信息

de Boeck H, Lories V, David G, Cassiman J J, van den Berghe H

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Biochem J. 1987 Nov 1;247(3):765-71. doi: 10.1042/bj2470765.

Abstract

Human lung fibroblasts produce heparan sulphate proteoglycans (HSPG) that are associated with the plasma membrane. A monoclonal-antibody (Mab)-secreting hybridoma, S1, was produced by fusion of SP 2/0-AG 14 mouse myeloma cells with spleen cells from mice immunized with partially purified cellular HSPG fractions. The HSPG character of the material carrying the epitope recognized by Mab S1 was demonstrated by: (i) the co-purification of the S1 epitope with the membrane HSPG of human lung fibroblasts; (ii) the decrease in size of the material carrying the S1 epitope upon treatment with heparinase or heparitinase, and the resistance of this material to heparinase treatment after N-desulphation. The S1 epitope appears to be part of the core protein, since it was destroyed by proteinase treatment and by disulphide-bond reduction, but not by treatments that depolymerize the glycosaminoglycan chains and N-linked oligosaccharide chains. Polyacrylamide-gel electrophoresis of non-reduced heparitinase-digested membrane HSPG followed by Western blotting and immunostaining with Mab S1 revealed a single band with apparent molecular mass of 64 kDa. Membrane proteoglycans isolated from detergent extracts or from 4 M-guanidinium chloride extracts of the cells yielded similar results. Additional digestion with N-glycanase lowered the apparent molecular mass of the immunoreactive material to 56 kDa, suggesting that the core protein also carries N-linked oligosaccharides. Fractionation of 125I-labelled membrane HSPG by immuno-affinity chromatography on immobilized Mab S1, followed by heparitinase digestion and polyacrylamide-gel electrophoresis of the bound material, yielded a single labelled band with apparent molecular mass 64 kDa. Treatment with dithiothreitol caused a slight increase in apparent molecular mass, suggesting that the core protein of this membrane proteoglycan of a single subunit containing (an) intrachain disulphide bond(s).

摘要

人肺成纤维细胞产生与质膜相关的硫酸乙酰肝素蛋白聚糖(HSPG)。通过将SP 2/0-AG 14小鼠骨髓瘤细胞与用部分纯化的细胞HSPG组分免疫的小鼠脾细胞融合,产生了一种分泌单克隆抗体(Mab)的杂交瘤S1。携带Mab S1识别的表位的物质的HSPG特性通过以下方式得以证明:(i)S1表位与人肺成纤维细胞的膜HSPG共纯化;(ii)用肝素酶或硫酸乙酰肝素酶处理后,携带S1表位的物质大小减小,且该物质在N-去硫酸化后对肝素酶处理具有抗性。S1表位似乎是核心蛋白的一部分,因为它在蛋白酶处理和二硫键还原后被破坏,但在使糖胺聚糖链和N-连接寡糖链解聚的处理后未被破坏。对未还原的硫酸乙酰肝素酶消化的膜HSPG进行聚丙烯酰胺凝胶电泳,然后进行Western印迹并用Mab S1进行免疫染色,显示出一条表观分子量为64 kDa的单条带。从细胞的去污剂提取物或4 M盐酸胍提取物中分离的膜蛋白聚糖产生了类似的结果。用N-聚糖酶进一步消化使免疫反应性物质的表观分子量降至56 kDa,表明核心蛋白也携带N-连接寡糖。通过在固定化的Mab S1上进行免疫亲和色谱对125I标记的膜HSPG进行分级分离,然后对结合物质进行硫酸乙酰肝素酶消化和聚丙烯酰胺凝胶电泳,得到一条表观分子量为64 kDa的单条标记带。用二硫苏糖醇处理导致表观分子量略有增加,表明这种膜蛋白聚糖的核心蛋白是一个含有链内二硫键的单亚基。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a062/1148477/18774a33589b/biochemj00244-0266-a.jpg

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