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A role for polyglucans in a model sea urchin embryo cellular interaction

机译:聚葡聚糖在模型海胆胚胎细胞相互作用中的作用

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The enzymatic activities of commercially prepared glycosidases were verified by direct chemical assays using defined substrates and fixed and live sea urchin (Lytechinus pictus) embryos to determine if a model cellular interaction of interest to developmental biologists for over a century (interaction of archenteron tip and roof of the blastocoel) wasmediated by glycans. Glycosidases (active and denatured) were incubated with microdissected archenterons and blastocoel roofs in a direct assay to learn if their enzymatic activities could prevent the normal adhesive interaction. Of the five glycosidases tested only β-amylase (an exoglycosidase) immediately inhibited the interaction at relatively low unit activity. α-Amylase (an endoglycosidase) had no measurable effect, while other glycosidases (α-glucosidase, β-glucosidase, β-galactosidase) only substantially inhibited adhesion after a 12-h incubation. We demonstrated that the five glycosidases were active (not inhibited) in the presence of embryo materials, and that cleaved sugars could be detected directly after incubation of some enzymes with the embryos. The biochemical purity of the enzymes was examined using gel electrophoresis under denaturing conditions, and the absence of contaminating proteases was confirmed using AzocollTM substrate. As we cannot entirely rule out the presence of minor contaminating enzymatic activities, only inhibitions of adhesion after very short incubations with enzyme were considered significant and biologically relevant. Although glycans in indirect experiments have been implicated in mediating the interaction of the tip of the archenteron and roof of the blastocoel, to our knowledge, this is the first study that directly implicates polyglucans with terminal 1,4-linked glucose residues in this adhesive event.
机译:商业化制备的糖苷酶的酶活性通过使用定义的底物和固定的和活的海胆(Lytechinus pictus)胚胎通过直接化学测定法进行验证,以确定在一个多世纪内发育生物学家是否感兴趣的模型细胞相互作用(弓形虫尖端与屋顶的相互作用)囊胚的“糖原”是由聚糖介导的。在直接测定中,将糖苷酶(活性的和变性的)与微解剖的肠动物和囊胚顶一起孵育,以了解其酶活性是否可以阻止正常的胶粘剂相互作用。在所测试的五个糖苷酶中,只有β-淀粉酶(一种糖苷外切酶)在相对较低的单位活性下立即抑制了相互作用。 α-淀粉酶(一种内切糖苷酶)没有可测量的作用,而其他糖苷酶(α-葡糖苷酶,β-葡糖苷酶,β-半乳糖苷酶)在孵育12小时后仅基本上抑制了粘附。我们证明了五个糖苷酶在存在胚胎物质的情况下是有活性的(未抑制),并且在将某些酶与胚胎孵育后可以直接检测到裂解的糖。在变性条件下使用凝胶电泳检查酶的生化纯度,并使用AzocollTM底物确认不存在污染的蛋白酶。由于我们不能完全排除轻微的污染性酶活性的存在,因此仅将与酶孵育时间短的抑制作用视为重要的,并且与生物学相关。尽管间接实验中的聚糖与介导原肠末端和囊胚顶的相互作用有关,但据我们所知,这是第一个直接将聚葡萄糖与末端1,4-连接的葡萄糖残基相关的研究。 。

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