课题基金 / 基金详情

Recognition and Deconstruction of Uronic Acid-Containing Polysaccharides

Recognition and Deconstruction of Uronic Acid-Containing Polysaccharides
含糖醛酸多糖的识别与解构
批准号:
RGPIN-2014-05018
负责人:
Suits, Michael
金额:
$2.91万
依托单位:
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

项目摘要

项目成果

Suits, Michael的其他基金

相似基金

相关文献

中文摘要
翻译
除了公认的碳水化合物作为营养来源的作用外,多糖、蛋白聚糖和糖脂等形式的复合碳水化合物可以被认为是“细胞的语言”,因为它们介导了许多完整的生物事件。为了破译一类碳水化合物,含糖醛酸多糖(UCPs)在这些过程中所起的作用,我将继续研究与碳水化合物识别和代谢有关的蛋白质的结构和功能特征。ucp在组成上是相似的,它们由重复的元素组成,包括- d -葡萄糖醛酸、- d -半乳糖醛酸、- d -4- o -甲基葡萄糖醛酸或它们沿链长度的衍生物。然而,尽管这种成分相似,ucp介导许多不同的生物相互作用和细胞信号传导事件。例如:ucp在细胞和组织表面具有独特的机械、粘弹性和渗透电位,它们参与整个细胞外基质中的配体、营养物质和细胞运动,并与各种效应分子相互作用以介导细胞内相互作用。虽然我的研究的长期目标是一般地解决ucp,但最初的重点将放在两种碳水化合物上,透明质酸和果胶(高半乳糖酸)。本研究的重点是基于这样的假设:微生物系统对UCP代谢的结构和功能重建将弥合UCP组成的细微差异及其多样化的生物学功能之间的知识差距。尽管透明质酸和果胶代谢作为无毒复合材料具有重要的生物学意义和工业意义,但它们是糖生物学中一个尚未充分开发的分支。例如,在过去的三年中,一类新的果胶降解酶被报道,我自己的工作已经确定了第一个微生物透明质酸结合蛋白。因此,我应用了基于发现的生物信息学方法来鉴定一系列新的透明质酸和果胶相关基因,这将是我们提出的研究计划的重点。该项目的长期目标是通过三维结构测定来研究透明质酸和果胶的识别和代谢蛋白质因子,并使用支持动力学和热力学技术来探测分子相互作用和作用机制。具体来说,我和我的学员将使用x射线晶体学和小角度x射线散射进行结构表征,以及各种互补的分子表征技术,包括生物信息学、糖生物学、酶学、量热学和蛋白质生物化学,来关联结构和功能。这种统一的分子表征和功能分析方法将使我们能够从多个角度解决重要的生物过程,并增强我们研究计划总体目标的影响,这是丰富我们对透明质酸和果胶代谢的理解;两种突出的多糖,分别在细胞外基质和植物细胞壁的生物事件协调中做出了相当大的贡献。
英文摘要
Beyond the universally recognized role for carbohydrates as nutrient sources, complex carbohydrates in the form of polysaccharides, proteoglycans, and glycolipids may be considered to be the “the language of the cell” in that they mediate many integral biological events. In an effort to decipher the role that a class of carbohydrates, the uronic-acid containing polysaccharides (UCPs), play in these processes, I will pursue the structural and functional characterization of the proteins involved in carbohydrate recognition and metabolism. UCPs are compositionally similar in that they are made up of repeating elements that include either beta-D-glucuronic acid, alpha-D-galacturonic acid, alpha-D-4-O-methylglucuronic acid, or their derivatives along the chain lengths. However, despite this compositional similarity, UCPs mediate many diverse biological interactions and cell-signaling events. For example: UCPs contribute unique mechanical, viscoelastic, and osmotic potential at cell and tissue surfaces they participate in ligand, nutrient, and cellular motility throughout the extracellular matrix, and they interact with a variety of effector molecules to mediate intracellular interactions. While the long-term objective of my research will address UCPs in general, the initial focus will be on two carbohydrates in particular, hyaluronan and pectin (homogalacturonate). This research focus is based on the hypothesis: that structural and functional reconstruction of microbial systems for UCP metabolism will bridge the knowledge gap between subtle differences in UCP composition and their diverse biological functions. Despite their biological significance and industrial relevance as non-toxic composites, hyaluronan and pectin metabolism is a largely underexplored branch of glycobiology. For example, a novel class of pectin-degrading enzymes has been reported within the past three years and my own work has identified the first microbial hyaluronan binding protein. I have therefore applied a discovery-based bioinformatics approach to identify a series of novel hyaluronan and pectin-related genes that will be the focus of our proposed research program. The long-term objective of the program is to study hyaluronan and pectin recognition and metabolizing protein factors by 3-D structure determination, and to use supportive kinetic and thermodynamic techniques to probe molecular interactions and mechanisms of action. Specifically, my trainees and I will use X-ray crystallography and Small Angle X-ray Scattering for structural characterization and various complementary molecular characterization techniques, including bioinformatics, glycobiology, enzymology, calorimetry and protein biochemistry, to correlate structure and function. This unified approach to molecular characterization and functional analyses will allow us to address important biological processes from multiple perspectives and enhances the impact of the overarching objective of our research program, which is to enrich our understanding of hyaluronan and pectin metabolism; two prominent polysaccharides that make considerable contributions to the coordination of biological events in the extracellular matrix and plant cell walls, respectively.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Oral Biofilm Dispersal Strategies
  • 批准号:
    RGPIN-2022-05457
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $2.33万
  • 财政年份:
    2022
  • 负责人:
    Suits, Michael
  • 依托单位:
MECHANISMS OF MICROBIAL CROSSTALK AND BIOFILM METABOLISM IN THE ORAL CAVITY
  • 批准号:
    DDG-2020-00007
  • 项目类别:
    Discovery Development Grant
  • 资助金额:
    $1.09万
  • 财政年份:
    2021
  • 负责人:
    Suits, Michael
  • 依托单位:
MECHANISMS OF MICROBIAL CROSSTALK AND BIOFILM METABOLISM IN THE ORAL CAVITY
  • 批准号:
    DDG-2020-00007
  • 项目类别:
    Discovery Development Grant
  • 资助金额:
    $1.09万
  • 财政年份:
    2020
  • 负责人:
    Suits, Michael
  • 依托单位:
Recognition and Deconstruction of Uronic Acid-Containing Polysaccharides
  • 批准号:
    RGPIN-2014-05018
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $2.91万
  • 财政年份:
    2019
  • 负责人:
    Suits, Michael
  • 依托单位:
海外基金