{"title":"糖组学相关氨基酸应用的最新进展综述","authors":"Simone Mi, Houston Ta","doi":"10.4172/2153-0637.1000E124","DOIUrl":null,"url":null,"abstract":"BOH) have been utilised in a wide range of applications, including as reaction promoters and catalysts [1-4] as dyes,[5] as support for derivatisation and affinity purification of diols, sugars and glycosylated proteins,[6] as sensors for carbohydrates,[7-8] as protecting or activating groups in carbohydrate synthesis,[9-12] as separation or membrane transport tools,[13-15] and as a pharmacophore in medicinal chemistry.[16-17] Here, the authors would like to focus on the most recent advances (mainly the past 5 years) in the applications of boronic acids important to the “glycosciences” and related fields.Fluorescence-based saccharide sensing using boronic acid-based entities has been investigated for nearly 25 years[18-21] because it is recognized that boronic acids have the potential to afford semi-invasive or non-invasive monitoring of carbohydrate levels in a variety of medical conditions, including cancer and diabetes. Glucose-level monitoring is of paramount importance to limit the long-term consequences of diabetes mellitus (e.g. damage to the heart, eyes, kidneys, nerves and other organs caused by malign glycation of vital protein structures). [22] A number of challenges still require improvement, including increased discrimination between monosaccharides, functioning under physiological conditions and sensor stability towards photobleaching or oxidation. [23,24] The relative binding constants (K) of monosaccharides with boronic acids reveal glucose to be a weak boronic acid binder,[25] and D-fructose a strong binder which presents a problem in the development of glucose-selective artificial receptors. This issue has been partially ameliorated by the utilization of diboronates. However, these bulkier sensors tend to be less water soluble than their monoboronate counterparts. [23-24] Increasing the sensor’s water solubility profile, whilst still retaining the low pKa values for binding at neutral pH, has been achieved by introduction of a pyridiniumboronic acid unit in the sensor molecule [26-27].Recent advances in this field include the bisanthracene diboronic acids (e.g. 1, figure 1) developed by Wang and co-workers,[28] which showed that the careful balance of orientation and distance between the two boronic acids results in sensors, such as 2, that can bind selectively to D-glucose over D-fructose (K = 1472 M","PeriodicalId":89585,"journal":{"name":"Journal of glycomics & lipidomics","volume":"4 1","pages":"1-5"},"PeriodicalIF":0.0000,"publicationDate":"2014-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2153-0637.1000E124","citationCount":"3","resultStr":"{\"title\":\"A Brief Overview of Recent Advances in the Applications of Boro nic Acids Relevant to Glycomics\",\"authors\":\"Simone Mi, Houston Ta\",\"doi\":\"10.4172/2153-0637.1000E124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BOH) have been utilised in a wide range of applications, including as reaction promoters and catalysts [1-4] as dyes,[5] as support for derivatisation and affinity purification of diols, sugars and glycosylated proteins,[6] as sensors for carbohydrates,[7-8] as protecting or activating groups in carbohydrate synthesis,[9-12] as separation or membrane transport tools,[13-15] and as a pharmacophore in medicinal chemistry.[16-17] Here, the authors would like to focus on the most recent advances (mainly the past 5 years) in the applications of boronic acids important to the “glycosciences” and related fields.Fluorescence-based saccharide sensing using boronic acid-based entities has been investigated for nearly 25 years[18-21] because it is recognized that boronic acids have the potential to afford semi-invasive or non-invasive monitoring of carbohydrate levels in a variety of medical conditions, including cancer and diabetes. Glucose-level monitoring is of paramount importance to limit the long-term consequences of diabetes mellitus (e.g. damage to the heart, eyes, kidneys, nerves and other organs caused by malign glycation of vital protein structures). [22] A number of challenges still require improvement, including increased discrimination between monosaccharides, functioning under physiological conditions and sensor stability towards photobleaching or oxidation. [23,24] The relative binding constants (K) of monosaccharides with boronic acids reveal glucose to be a weak boronic acid binder,[25] and D-fructose a strong binder which presents a problem in the development of glucose-selective artificial receptors. This issue has been partially ameliorated by the utilization of diboronates. However, these bulkier sensors tend to be less water soluble than their monoboronate counterparts. [23-24] Increasing the sensor’s water solubility profile, whilst still retaining the low pKa values for binding at neutral pH, has been achieved by introduction of a pyridiniumboronic acid unit in the sensor molecule [26-27].Recent advances in this field include the bisanthracene diboronic acids (e.g. 1, figure 1) developed by Wang and co-workers,[28] which showed that the careful balance of orientation and distance between the two boronic acids results in sensors, such as 2, that can bind selectively to D-glucose over D-fructose (K = 1472 M\",\"PeriodicalId\":89585,\"journal\":{\"name\":\"Journal of glycomics & lipidomics\",\"volume\":\"4 1\",\"pages\":\"1-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.4172/2153-0637.1000E124\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of glycomics & lipidomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2153-0637.1000E124\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of glycomics & lipidomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2153-0637.1000E124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
BOH)已被广泛应用,包括作为反应促进剂和催化剂[1-4]作为染料,[5]作为二醇、糖和糖基化蛋白衍生化和亲和纯化的支持,[6]作为碳水化合物的传感器,[7-8]作为碳水化合物合成中的保护或激活基团,[9-12]作为分离或膜运输工具,[13-15]以及作为药物化学中的药效团。[16-17]在这里,作者希望重点介绍硼酸在“糖科学”及相关领域的应用的最新进展(主要是过去5年)。使用硼酸为基础的实体进行基于荧光的糖类传感已经研究了近25年[18-21],因为人们认识到硼酸具有在各种医疗条件下(包括癌症和糖尿病)提供半侵入性或非侵入性碳水化合物水平监测的潜力。血糖水平监测对于限制糖尿病的长期后果(如重要蛋白质结构的恶性糖化对心脏、眼睛、肾脏、神经和其他器官的损害)至关重要。[22]许多挑战仍然需要改进,包括单糖之间的区别增加,生理条件下的功能和传感器对光漂白或氧化的稳定性。[23,24]单糖与硼酸的相对结合常数(K)表明葡萄糖是弱硼酸结合剂,[25]和d -果糖是强结合剂,这给葡萄糖选择性人工受体的开发带来了一个问题。二硼酸盐的使用部分地改善了这个问题。然而,这些体积较大的传感器往往比它们的单硼酸盐对应物更不溶于水。[23-24]通过在传感器分子中引入吡啶硼酸单元,可以提高传感器的水溶性,同时在中性pH下仍能保持较低的pKa值[26-27]。该领域的最新进展包括Wang及其同事开发的双蒽二硼酸(例如1,图1)[28],该研究表明,两种硼酸之间的取向和距离的仔细平衡导致传感器,如2,可以选择性地结合d -葡萄糖而不是d -果糖(K = 1472 M)
A Brief Overview of Recent Advances in the Applications of Boro nic Acids Relevant to Glycomics
BOH) have been utilised in a wide range of applications, including as reaction promoters and catalysts [1-4] as dyes,[5] as support for derivatisation and affinity purification of diols, sugars and glycosylated proteins,[6] as sensors for carbohydrates,[7-8] as protecting or activating groups in carbohydrate synthesis,[9-12] as separation or membrane transport tools,[13-15] and as a pharmacophore in medicinal chemistry.[16-17] Here, the authors would like to focus on the most recent advances (mainly the past 5 years) in the applications of boronic acids important to the “glycosciences” and related fields.Fluorescence-based saccharide sensing using boronic acid-based entities has been investigated for nearly 25 years[18-21] because it is recognized that boronic acids have the potential to afford semi-invasive or non-invasive monitoring of carbohydrate levels in a variety of medical conditions, including cancer and diabetes. Glucose-level monitoring is of paramount importance to limit the long-term consequences of diabetes mellitus (e.g. damage to the heart, eyes, kidneys, nerves and other organs caused by malign glycation of vital protein structures). [22] A number of challenges still require improvement, including increased discrimination between monosaccharides, functioning under physiological conditions and sensor stability towards photobleaching or oxidation. [23,24] The relative binding constants (K) of monosaccharides with boronic acids reveal glucose to be a weak boronic acid binder,[25] and D-fructose a strong binder which presents a problem in the development of glucose-selective artificial receptors. This issue has been partially ameliorated by the utilization of diboronates. However, these bulkier sensors tend to be less water soluble than their monoboronate counterparts. [23-24] Increasing the sensor’s water solubility profile, whilst still retaining the low pKa values for binding at neutral pH, has been achieved by introduction of a pyridiniumboronic acid unit in the sensor molecule [26-27].Recent advances in this field include the bisanthracene diboronic acids (e.g. 1, figure 1) developed by Wang and co-workers,[28] which showed that the careful balance of orientation and distance between the two boronic acids results in sensors, such as 2, that can bind selectively to D-glucose over D-fructose (K = 1472 M