Sangadala S, Wallace P, Mendicino J
Department of Biochemistry, University of Georgia, Athens 30602.
Mol Cell Biochem. 1991 Jul 24;106(1):1-14. doi: 10.1007/BF00231183.
RNA was isolated from cultured swine trachea epithelial cells and mucus-secreting tumor cell lines from human pancreas, lung and colon by extraction with guanidine isothiocyanate. Poly(A)+mRNA rich fractions were purified by repeated chromatography on oligo (dT)-cellulose columns and they were translated in a cell-free rabbit reticulocyte system. Translation products labelled with 35S-methionine were isolated by immunoprecipitation with specific antibodies to the polypeptide chains of mucin glycoproteins and they were analyzed by SDS-PAGE and fluorography. A single principal polypeptide band of 67 kDa was found in all cases when the immunoprecipitates were washed with buffer containing bovine serum albumin and unlabeled deglycosylated mucin glycoprotein. The intensity of the 67 kDa band decreased when unlabeled deglycosylated mucin glycoprotein was added to the translation mixture before immunoprecipitation. Affinity purified monospecific antibodies elicited against chemically deglycosylated polypeptide chains of purified mucin glycoproteins from human and swine trachea and Cowper's gland were all equally effective in immunoprecipitating the 67 kDa translation product. Monospecific antibodies directed against the glycosylated and unglycosylated regions of the polypeptide chain yielded single bands with a molecular size of 67 kDa in each case. Peptide profiles obtained by digestion of the 67 kDa translation product with S. aureus V-8 protease were identical to those obtained with deglycosylated human and swine trachea mucin glycoproteins. These studies clearly demonstrate that the translation product of swine trachea and human lung, colon and pancreatic mucin glycoprotein gene is a single polypeptide chain of 67 kDa. The relative size and properties of the translation products synthesized with poly (A)+RNA isolated from mucus-secreting cells derived from three different tissues are similar to those of mucin glycoproteins purified directly from mucus secretions of human and swine trachea epithelium.
采用异硫氰酸胍提取法,从培养的猪气管上皮细胞以及来自人胰腺、肺和结肠的黏液分泌肿瘤细胞系中分离RNA。通过在寡聚(dT)纤维素柱上反复层析,纯化富含多聚腺苷酸(Poly(A)+)的mRNA组分,并在无细胞兔网织红细胞系统中进行翻译。用针对黏蛋白糖蛋白多肽链的特异性抗体进行免疫沉淀,分离出用35S-甲硫氨酸标记的翻译产物,然后通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和荧光自显影进行分析。当用含有牛血清白蛋白和未标记去糖基化黏蛋白糖蛋白的缓冲液洗涤免疫沉淀物时,在所有情况下均发现一条67 kDa的主要多肽带。在免疫沉淀前将未标记的去糖基化黏蛋白糖蛋白添加到翻译混合物中时,67 kDa条带的强度降低。针对来自人和猪气管及尿道球腺的纯化黏蛋白糖蛋白的化学去糖基化多肽链产生的亲和纯化单特异性抗体,在免疫沉淀67 kDa翻译产物方面均同样有效。针对多肽链糖基化和非糖基化区域的单特异性抗体在每种情况下均产生分子大小为67 kDa的单一条带。用金黄色葡萄球菌V-8蛋白酶消化67 kDa翻译产物获得的肽谱,与用去糖基化的人和猪气管黏蛋白糖蛋白获得的肽谱相同。这些研究清楚地表明,猪气管以及人肺、结肠和胰腺黏蛋白糖蛋白基因的翻译产物是一条67 kDa的单多肽链。用从三种不同组织的黏液分泌细胞中分离的多聚腺苷酸(Poly(A)+)RNA合成的翻译产物的相对大小和特性,与直接从人和猪气管上皮黏液分泌物中纯化的黏蛋白糖蛋白相似。