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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Sensitive glycoprofiling of insulin-like growth factor receptors isolated from colon tissue of patients with colorectal carcinoma using lectin-based protein microarray
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Sensitive glycoprofiling of insulin-like growth factor receptors isolated from colon tissue of patients with colorectal carcinoma using lectin-based protein microarray

机译:使用凝集素的蛋白质微阵列,从结肠直肠癌结肠组织中分离的胰岛素样生长因子受体的敏感性糖过细胞

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Glycosylation of cell receptors influences their function and development of tumour induces changes in glycosylation. Cell growth depends on the activation of receptors which bind growth factors and the insulin-like growth factor (IGF) receptors are among the most important ones. Usually, only small quantities of isolated receptors are available thus there is a need of suitable assay to study receptors glycosylation. Therefore, we developed a lectin-based reverse-phase protein microarray method for screening the glycosylation pattern of receptors in picomolar (pM) concentrations. The method was applied to glycoprofile IGF1 and IGF2 receptors and the solubilised membrane proteins isolated from tumour and nontumour colon tissue of patients with colorectal cancer. We found that common to both receptors was partial overlapping of the major glycan structures with those present in the entire glycome of membrane proteins. In contrast, receptors possess higher level of alpha 2,3 sialic acid residues and lower level of tri-/tetra-antennary complex type N-glycans and terminal mannose in high-mannose structures. Increased levels of fucosylation and branched mannose structures were observed in both receptors derived from tumour tissue compared to non-tumour tissue. The described method enabling glycan analysis of receptors has a big application potential in e.g. biomarker research, biology and diagnostics. (C) 2019 Elsevier B.V. All rights reserved.
机译:细胞受体的糖基化影响其功能和肿瘤的发育诱导糖基化的变化。细胞生长取决于引起生长因子和胰岛素样生长因子(IGF)受体是最重要的受体的激活。通常,只有少量的分离受体可获得,因此需要具有合适的测定来研究受体糖基化。因此,我们开发了一种基于凝集素的反向相蛋白微阵列方法,用于筛选皮摩尔(PM)浓度的受体的糖基化图案。将该方法应用于糖基丙酮酰基和IGF2受体和从结肠直肠癌患者的肿瘤和非肿瘤结肠组织中分离的增溶膜蛋白。我们发现,两个受体的共同认为主要聚糖结构与存在于膜蛋白的整个Glyce中的主要聚糖结构的部分重叠。相反,受体具有较高水平的α2,3唾液酸残基,并且在高甘露糖结构中具有较低的三烯型络合物型N-聚糖和末端甘露糖。与非肿瘤组织相比,在衍生自肿瘤组织的两个受体中观察到岩藻糖基化和支链甘露糖结构的增加。所描述的方法,使得具有受体的聚糖分析具有大的应用潜力。生物标志物研究,生物学和诊断。 (c)2019 Elsevier B.v.保留所有权利。

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