聚糖
DNA微阵列
微阵列
蛋白质组学
蛋白质微阵列
糖组学
计算生物学
蛋白质阵列分析
表位
生物
化学
糖蛋白
生物化学
基因
基因表达
抗体
遗传学
作者
William G. T. Willats,Svend Erik Rasmussen,Tina Kristensen,Jørn Dalgaard Mikkelsen,John Knox
出处
期刊:Proteomics
[Wiley]
日期:2002-12-01
卷期号:2 (12): 1666-1671
被引量:163
标识
DOI:10.1002/1615-9861(200212)2:12<1666::aid-prot1666>3.0.co;2-e
摘要
The development of DNA and protein microarrays represents a significant advance in transcriptomics and proteomics research. Such arrays allow the high-throughput, parallel analysis of protein occurrence and interactions and gene expression. However, this advance has not been matched by equivalent technology for analysis of glycomes. One reason for this is that compared to proteins, it is difficult to reliably immobilise populations of chemically and structurally diverse glycans. We describe the development of a new microarray slide surface to which diverse glycan structures can be directly immobilised without prior derivatisation of the slide surface or any modification of the arrayed samples. The slides can be used to produce comprehensive microarrays of carbohydrates, glycoproteins and proteoglycans using isolated samples or cell extracts. Using standard microarray equipment, a series of carbohydrate microarrays were generated and probed with a panel of monoclonal antibodies with specificities for glycan epitopes. The arrays were highly reproducible, stable, and could be stored dry for several months. Glycans play central roles in development, carcinogenesis, cell adhesion, and immunity and are increasingly the subject of therapeutic approaches. We anticipate that the development of carbohydrate microarrays will be important for the high-throughput analysis of glycans and their molecular interactions.
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