Evaluating SPR array imaging for glycobiology

评估糖生物学的 SPR 阵列成像

• 批准号: BB/G024464/1
• 负责人: David Russell
• 金额: $ 0.22万
• 依托单位: University of East Anglia
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2009
• 资助国家: 英国
• 起止时间: 2009 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FG024464%2F1
• 关键词: Evaluating; SPR; array; imaging; glycobiology

Whilst carbohydrate structure and recognition are clearly central to biology, our appreciation of their structure and function is still rudimentary compared to proteins and nucleic acids. It has been estimated that around 2% of the human genome is dedicated to glyco-active enzymes (up to 6% in plants) and that over 70% of all proteins in man are glycosylated. In turn this has led to a need for analysis of larger numbers of glycan structures, and their cognate binding proteins, which has provided the impetus for the development of new technologies with high-throughput potential. Latterly, glycoscientists have identified carbohydrate microarrays (glycoarrays) as a key tool for the high-throughput studies that are necessary to understand this complex area of biology. The purpose of this study is to evaluate new methods with which to analyse carbohydrate-active enzymes based on integrated, chip-based surface plasmon resonance spectroscopy-mass spectrometry.

虽然碳水化合物的结构和识别显然是生物学的核心，但与蛋白质和核酸相比，我们对它们的结构和功能的理解仍然是基本的。据估计，人类基因组的约2%是专门用于糖活性酶（在植物中高达6%），并且人类中超过70%的蛋白质是糖基化的。反过来，这导致需要分析大量的聚糖结构及其同源结合蛋白，这为开发具有高通量潜力的新技术提供了动力。最近，糖科学家已经确定了碳水化合物微阵列（glycoarrays）作为高通量研究的关键工具，这是理解生物学这一复杂领域所必需的。本研究的目的是评估新的方法，分析碳水化合物活性酶的基础上集成，基于芯片的表面等离子体共振光谱-质谱。