Fahim R E, Specian R D, Forstner G G, Forstner J F
Department of Biochemistry, Hospital for Sick Children, Toronto, Ontario, Canada.
Biochem J. 1987 May 1;243(3):631-40. doi: 10.1042/bj2430631.
Rat intestinal mucin is polymerized by a putative 'link' component of Mr 118,000 that can be released from the native mucin by thiol reduction [Fahim, Forstner & Forstner (1983) Biochem. J. 209, 117-124]. To confirm that this component is an integral part of the mucin and independent of the mucin purification technique, rat mucin was purified in the present study by three independent techniques. In all cases, the 118,000-Mr component was released after reduction. The 118 kDa band was electroeluted from SDS/polyacrylamide gels and its composition shown to resemble closely that of the link component of human intestinal mucin [Mantle, Forstner & Forstner (1984) Biochem. J. 224, 345-354]. Carbohydrates were present, including significant (10 mol/100 mol) amounts of mannose, suggesting the presence of N-linked oligosaccharides. Monospecific antibodies prepared against the rat 118,000-Mr component established its tissue localization in intestinal goblet cells. Mucins subjected to SDS/polyacrylamide-gel electrophoresis and Western blots using the same antibody, established that the link components of rat and human intestinal mucin are similar antigenically. Brief exposure (10 min) of native rat mucin to trypsin or Pronase (enzyme/mucin protein, 1:500, w/w) also released a 118,000-Mr component that reacted with the monospecific antibody. Thus the 118,000-Mr component is an integral part of the mucin and, although linked to large glycopeptides by disulphide bonds, this component also has proteinase-sensitive peptide bonds, presumably at terminal locations such that brief treatment with proteinases releases the molecule in a reasonably intact form. Under physiological conditions, therefore, one might expect that, after mucin is secreted into the intestinal lumen, luminal proteinases would rapidly remove the link component, thereby causing the mucin to depolymerize.
大鼠肠道粘蛋白由一种假定的分子量为118,000的“连接”成分聚合而成,该成分可通过巯基还原从天然粘蛋白中释放出来[法希姆、福斯特纳和福斯特纳(1983年)《生物化学杂志》209卷,第117 - 124页]。为了证实该成分是粘蛋白的一个组成部分且与粘蛋白纯化技术无关,本研究采用三种独立技术对大鼠粘蛋白进行了纯化。在所有情况下,还原后都释放出了分子量为118,000的成分。从SDS/聚丙烯酰胺凝胶中电洗脱118 kDa条带,并显示其组成与人类肠道粘蛋白的连接成分极为相似[曼特尔、福斯特纳和福斯特纳(1984年)《生物化学杂志》224卷,第345 - 354页]。其中含有碳水化合物,包括大量(10摩尔/100摩尔)的甘露糖,提示存在N - 连接寡糖。针对大鼠分子量为118,000的成分制备的单特异性抗体确定了其在肠道杯状细胞中的组织定位。使用相同抗体对粘蛋白进行SDS/聚丙烯酰胺凝胶电泳和蛋白质免疫印迹分析,确定大鼠和人类肠道粘蛋白的连接成分在抗原性上相似。将天然大鼠粘蛋白短暂暴露(10分钟)于胰蛋白酶或链霉蛋白酶(酶/粘蛋白蛋白,1:500,w/w)也释放出一种能与单特异性抗体反应的分子量为118,000的成分。因此,分子量为118,000的成分是粘蛋白的一个组成部分,尽管它通过二硫键与大的糖肽相连,但该成分也有对蛋白酶敏感的肽键,推测位于末端位置,使得用蛋白酶短暂处理能以相当完整的形式释放该分子。因此,在生理条件下,可以预期,在粘蛋白分泌到肠腔后,腔内蛋白酶会迅速去除连接成分,从而导致粘蛋白解聚。