Chemical tools for mechanistic insights into O-mannosyl glycan biosynthesis

用于 O-甘露糖基聚糖生物合成机理洞察的化学工具

• 批准号: 2107410
• 金额: --
• 依托单位: University of York
• 依托单位国家: 英国
• 项目类别: Studentship
• 财政年份: 2018
• 资助国家: 英国
• 起止时间: 2018 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=studentship-2107410
• 关键词: Chemical; tools; mechanistic; insights; into

Proteins on the surface of cells are often modified with diverse, complex carbohydrate structures (glycans) that play key roles in a range of cellular processes including cell-cell and host-pathogen interactions. This project focuses on enzymes that are involved in the biosynthesis of O-mannosyl glycans, a type of glycan that is O-linked to threonine or serine residues and initiated by an aplha-linked mannose residue. This type of glycan is relatively poorly characterized, yet it is known to play fundamental roles in the interactions of cells with the extracellular matrix and with pathogens. Over the past decade there has been growing interest in O-mannosylation of the protein alpha-dystroglycan (alpha-DG), which plays essential roles in muscle tissue and the nervous system by linking the cytoskeleton with the extracellular matrix. Failure to assemble the correct O-mannosyl glycans on alpha-DG - due to a deficiency in one of the enzymes involved in their biosynthesis - causes a range of congenital muscular dystrophies and can also promote metastatic properties of cancer cells. However, the biosynthetic pathway of the O-mannosyl glycans on alpha-DG has only recently been elucidated (2016/2017), and although cellular roles for most enzymes have been assigned, much remains unclear regarding substrate specificity, mechanism of action, and factors regulating their localisation, stability and activity. Unfortunately, few tools are available to study the activity and mechanism of the enzymes involved. Using a chemical biology approach, this project aims to enhance our understanding of the mechanism of alpha-DG O-mannosylation, by focusing on two enzymes that play key roles in the biosynthesis of the glycan structure. Defects in these proteins impair the proper functioning of alpha-DG and thereby lead to specific types of congenital muscular dystrophies. We aim to combine structural studies with the use of novel chemical tools, which will be designed to act as substrate analogues for one or both of the enzymes of interest, to help improve our understanding of substrate binding and mechanism of the target enzymes. These results will also guide the design of novel inhibitors and probes that enable the functional analysis of the target enzymes. In order to reach these goals, we will use a cross-disciplinary approach that combines organic synthesis with biochemistry and structural biology. The student will initially focus on generating sufficient amounts of soluble protein to enable kinetic and structural studies. To enhance progress with the crystallography studies, the student will be supervised by Prof. Davies, and will benefit from the resources and expertise available in his laboratory. These experiments will further be facilitated by using substrate analogues synthesised by a second PhD student who will be starting at the same time. The mechanistic insights gained from these initial studies will then be used to design a new set of inhibitors and probes tailored to bind specifically within the enzyme active site. The student will synthesise these compounds and use them to study enzyme activity and mechanism in more detail. The student will thus receive a highly interdisciplinary training that includes chemical synthesis, in vitro assay development, gel electrophoresis and immunoblotting, bacterial and mammalian protein expression, purification of the enzymes of interest, and crystallisation techniques. This work will enhance our understanding of the molecular mechanisms underlying alpha-DG O-mannosylation and will lay the foundation for analysing the effects of molecular mutations in these enzymes. The development of probes and inhibitors for glycosyltransferases is a recurring challenge in the field of chemical biology and the development of such tools would thus be of significant value to the field.

细胞表面的蛋白质通常被不同的复杂碳水化合物结构（聚糖）修饰，这些结构在一系列细胞过程中发挥关键作用，包括细胞-细胞和宿主-病原体相互作用。该项目的重点是参与O-甘露糖基聚糖生物合成的酶，O-甘露糖基聚糖是一种与苏氨酸或丝氨酸残基O-连接并由aplha连接的甘露糖残基引发的聚糖。这种类型的聚糖的特征相对较差，但已知其在细胞与细胞外基质和病原体的相互作用中发挥重要作用。在过去的十年中，人们对α-肌营养不良蛋白聚糖（α-DG）的O-甘露糖基化越来越感兴趣，α-DG通过将细胞骨架与细胞外基质连接在肌肉组织和神经系统中发挥重要作用。由于参与其生物合成的酶之一缺乏，未能在α-DG上组装正确的O-甘露糖基聚糖-导致一系列先天性肌营养不良症，并且还可以促进癌细胞的转移特性。然而，α-DG上O-甘露糖基聚糖的生物合成途径最近才被阐明（2016/2017），尽管大多数酶的细胞作用已经被分配，但关于底物特异性，作用机制以及调节其定位，稳定性和活性的因素仍不清楚。不幸的是，很少有工具可用于研究所涉及的酶的活性和机制。使用化学生物学方法，该项目旨在通过关注在聚糖结构的生物合成中发挥关键作用的两种酶，增强我们对α-DG O-甘露糖基化机制的理解。这些蛋白质的缺陷会损害α-DG的正常功能，从而导致特定类型的先天性肌营养不良症。我们的目标是将联合收割机结构研究与新型化学工具的使用相结合，这些化学工具将被设计为作为感兴趣的一种或两种酶的底物类似物，以帮助提高我们对底物结合和靶酶机制的理解。这些结果也将指导新的抑制剂和探针的设计，使目标酶的功能分析。为了达到这些目标，我们将使用一种跨学科的方法，将有机合成与生物化学和结构生物学相结合。学生最初将专注于产生足够量的可溶性蛋白质，以进行动力学和结构研究。为了提高晶体学研究的进展，学生将由戴维斯教授监督，并将受益于他的实验室提供的资源和专业知识。这些实验将进一步促进使用底物类似物合成的第二个博士生谁将在同一时间开始。从这些初步研究中获得的机制见解将用于设计一组新的抑制剂和探针，这些抑制剂和探针被定制为在酶活性位点内特异性结合。学生将合成这些化合物，并使用它们来更详细地研究酶的活性和机制。因此，学生将接受高度跨学科的培训，包括化学合成，体外分析开发，凝胶电泳和免疫印迹，细菌和哺乳动物蛋白质表达，感兴趣的酶的纯化和结晶技术。这项工作将提高我们对α-DG O-甘露糖基化的分子机制的理解，并为分析这些酶中分子突变的影响奠定基础。用于糖基转移酶的探针和抑制剂的开发是化学生物学领域中反复出现的挑战，并且此类工具的开发因此将对该领域具有重要价值。