Hauri H P, Kedinger M, Haffen K, Freiburghaus A, Grenier J F, Hadorn B
Biochim Biophys Acta. 1977 Jun 16;467(3):327-39. doi: 10.1016/0005-2736(77)90310-8.
The incorporation of [14C]glucosamine into brush border glycoproteins by human small intestinal mucosa in organ culture has been investigated. The experiments were based on the observations that (1) isolated brush border membrane fragments from cultured explants showed an unchanged pattern of protein bands and brush border enzyme activities on sodium dodecyl sulfate/polyacrylamide gels after electrophoresis and (2) the rate of overall [14C]glucosamine incorporation measured in the tissue homogenate remained constant up to 48 h. After 24 h of culture, the radioactivity peaks on gels due to incorporation of [14C]glucosamine were found exclusively in the high molecular weight region and corresponded to protein bands identified as maltase-glucoamylase, lactase, sucrase-isomaltase, enterokinase and alkaline phosphatase. Enzymatic activity could not be assigned to the three remaining labelled bands. Most of these glycoproteins were already labelled after 5 h. Newly glycosylated brush border enzymes remained predominantly associated with the brush border membrane of intact cells with little release into the medium up to 24 h.
已对人体小肠黏膜在器官培养中[14C]葡糖胺掺入刷状缘糖蛋白的情况进行了研究。这些实验基于以下观察结果:(1)从培养的外植体中分离出的刷状缘膜片段在十二烷基硫酸钠/聚丙烯酰胺凝胶电泳后,蛋白质条带模式和刷状缘酶活性未发生变化;(2)在组织匀浆中测得的[14C]葡糖胺总体掺入率在长达48小时内保持恒定。培养24小时后,由于[14C]葡糖胺掺入而在凝胶上出现的放射性峰仅出现在高分子量区域,并且对应于被鉴定为麦芽糖酶 - 葡糖淀粉酶、乳糖酶、蔗糖酶 - 异麦芽糖酶、肠激酶和碱性磷酸酶的蛋白质条带。无法将酶活性归因于其余三个标记条带。这些糖蛋白中的大多数在5小时后就已被标记。新糖基化的刷状缘酶在长达24小时内主要仍与完整细胞的刷状缘膜相关联,很少释放到培养基中。