HUMAN FUCOSYLTRANSFERASE STRUCTURE/FUNCTION ANALYSIS

人岩藻糖基转移酶结构/功能分析

• 批准号: 6150220
• 负责人: Eric Holmes
• 金额: $ 34.31万
• 依托单位: NORTHWEST HOSPITAL AND MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-02-15 至 2002-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6150220
• 关键词: active sites; cell line; enzyme activity; enzyme structure; fucose; hexosyltransferase; human tissue; isozymes; protein structure function; receptor binding; site directed mutagenesis

DESCRIPTION: (adapted from the investigator's abstract) Expression of carbohydrate structures at the cell surface has been found to play an important role in many cellular processes, eg. cell-cell recognition, growth control, and receptor binding. Carbohydrates containing an a1A3-linked fucose on lacto- and neolacto-series core chains are found to be tumor-associated markers in many human cancers. Enzymes capable of catalyzing transfer of fucose into these acceptors have been identified and studied. Presently, at least six distinct a1A3 fucosyltransferases have been identified from human sources. Five of these enzymes have been cloned and their DNA and amino acid sequences determined. These enzymes are characterized by differences in enzymatic properties including acceptor specificity, kinetic properties, and distributions. This family of enzymes is an ideal system for studies of structure function relationships of glycosyltransferases. The research proposed in this application will take advantage of the multiplicity of enzyme forms and properties to identify specific residues and portions of the enzyme involved in substrate binding and catalysis. The initial focus will be on identifying by chemical means specific residues which have previously been determined to be essential for activity based upon results from site-specific chemical reagents. Examples include the GDP-frucose protected, N-ethylmaleamide-sensitive Cys residue present in eg. FT-III and -V and the GDP-fucose protected pyridoxal-P modifiable Lys residue present in each enzyme form. Other studies will use photoaffinity reagents to probe the binding sites for acceptor carbohydrates and donor GDP-fucose and analysis of acceptor binding properties through domain swapped variants. Site-directed mutagenesis and enzyme kinetic studies will be used to analyze the function of these sites in substrate binding and catalysis. These studies will provide information leading to a better understanding of enzyme function and, perhaps, a basis for differences in acceptor specificity. Another aim will focus on cloning and genetic characterization of a novel fucosyltransferase enzyme from NCI-H69 small cell lung carcinoma cells. This enzyme has properties distinct from other known forms. The research proposed in this application will lead to a greater understanding of enzyme complexity, structure-function relationships, and the nature of active sites in this family of enzymes having important function in disease processes.

描述：（改编自研究者摘要）表达 已经发现细胞表面的碳水化合物结构 在许多细胞过程中起重要作用，例如。 细胞-细胞识别， 生长控制和受体结合。 碳水化合物含有 发现乳糖和新乳糖系列核心链上的a1 A3-连接岩藻糖 在许多人类癌症中的肿瘤相关标志物。 酶能够 已经鉴定了催化岩藻糖转移到这些受体中， 研究了 目前，至少六种不同的α 1A 3岩藻糖基转移酶具有 从人类来源中发现的。 其中五种酶已被克隆 并测定了它们的DNA和氨基酸序列。 这些酶 其特征在于酶性质的差异，包括受体 特异性、动力学性质和分布。 这个酶家族 是一个理想的研究结构功能关系的系统， 糖基转移酶 本申请中提出的研究将采取 酶的形式和性质的多样性的优势，以确定 参与底物结合的酶的特定残基和部分 和催化作用。 最初的重点将是通过化学手段识别 先前已确定的特定残基对于 活性基于特定位点化学试剂的结果。 示例 包括GDP-果糖保护的N-乙基马来酰胺敏感的Cys残基 目前在EG。 FT-III和-V和GDP-岩藻糖保护的吡哆醛-P 每种酶形式中存在的可修饰的赖氨酸残基。 其他研究将使用 探测受体碳水化合物结合位点的光亲和试剂 和供体GDP-岩藻糖，并通过 域交换变体。 定点突变和酶动力学 研究将用于分析这些位点在底物中的功能 结合和催化。 这些研究将提供信息， 更好地了解酶的功能，也许， 受体特异性的差异。 另一个目标将集中在克隆和 NCI-H69中一种新型岩藻糖基转移酶的遗传特性 小细胞肺癌细胞 这种酶的特性与 其他已知的形式。 本申请中提出的研究将导致更大的 了解酶的复杂性，结构-功能关系， 在这个酶家族中的活性位点的性质具有重要的 在疾病过程中发挥作用。