Development of Genetically-Encoded Glucose Sensors

基因编码葡萄糖传感器的开发

• 批准号: 6691020
• 负责人: GUILLERMO A ALTENBERG
• 金额: $ 14.9万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-01-01 至 2004-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6691020
• 关键词: Development; Genetically; Encoded; Glucose; Sensors

DESCRIPTION (provided by applicant): In most living organisms, including animals, plants and bacteria, glucose is employed as energy source, for energy storage and in the synthesis of essential biological molecules. Glucose measurements are critical to elucidate the basic characteristics of glucose distribution at the cellular and subcellular level under normal conditions and in disease states. This is particularly important because in diabetes mellitus, one of the most common chronic diseases in humans, alterations in glucose metabolism (not well understood at the cell level) are the most important factor. Currently, there is no glucose sensor suitable for measuring glucose in cells and the sensors available for clinical and industrial applications are frequently unsatisfactory. This proposal presents a novel approach to develop glucose sensors based on the use of autofluorescent proteins (proteins that fluoresce in the absence of cofactors) and the glucose binding properties of the enzyme glucokinase (hexokinase IV), the glucose sensor protein of the pancreas. The most useful autofluorescent proteins derive from the green fluorescent protein from the jellyfish Aequoria victoria and the red fluorescent protein from a coral of the Discosoma genus (red fluorescent protein). Our plan is to develop a sensor that will be: 1) Suitable for "in vitro" measurements of glucose concentration, and 2) Genetically-encoded for targeting to specific cells and subcellular compartments, as well as specific cells and tissues of transgenic animals. The sensor can also be evaluated as the backbone for a continuous minimally invasive glucose monitoring system in diabetic patients. We plan to engineer glucose sensors by fusion of glucokinase to autofluorescent proteins. We will purify the sensor proteins expressed in E. coil, analyze their properties (fluorescence properties, response to glucose, specificity) and test their usefulness for measuring glucose in living cells. Although the goal of the project is to obtain a sensor for measurements in cells, to foster basic research under normal and disease conditions, potentially the new sensors can be adapted to industrial (e.g., glucose measurements in fruit juices) and medical (monitoring glycemia in diabetes mellitus) uses.

描述（由申请人提供）：在大多数生物体中，包括动物、植物和细菌，葡萄糖被用作能量来源，用于能量储存和合成必需的生物分子。葡萄糖测量对于阐明正常条件和疾病状态下细胞和亚细胞水平上葡萄糖分布的基本特征至关重要。这一点尤其重要，因为在糖尿病（人类最常见的慢性疾病之一）中，葡萄糖代谢的改变（在细胞水平上尚不清楚）是最重要的因素。目前，还没有适合测量细胞内葡萄糖的葡萄糖传感器，并且可用于临床和工业应用的传感器常常不能令人满意。该提案提出了一种开发葡萄糖传感器的新方法，该方法基于使用自发荧光蛋白（在没有辅因子的情况下发出荧光的蛋白质）和葡萄糖激酶（己糖激酶 IV）（胰腺的葡萄糖传感器蛋白）的葡萄糖结合特性。最有用的自发荧光蛋白源自维多利亚水母的绿色荧光蛋白和迪斯科马属珊瑚的红色荧光蛋白（红色荧光蛋白）。我们的计划是开发一种传感器，该传感器将：1）适合“体外”测量葡萄糖浓度，2）经过基因编码，针对特定细胞和亚细胞区室以及转基因动物的特定细胞和组织。该传感器还可作为糖尿病患者连续微创血糖监测系统的支柱进行评估。我们计划通过将葡萄糖激酶与自发荧光蛋白融合来设计葡萄糖传感器。 我们将纯化大肠杆菌中表达的传感器蛋白，分析它们的特性（荧光特性、对葡萄糖的响应、特异性）并测试它们在测量活细胞中葡萄糖的有用性。 尽管该项目的目标是获得用于细胞测量的传感器，以促进正常和疾病条件下的基础研究，但新传感器有可能适用于工业（例如，果汁中的葡萄糖测量）和医疗（监测血糖）糖尿病）用途。