Department of Chemistry and Environmental Science, Zhangzhou Normal College, Zhangzhou 363000, PR China.
Spectrochim Acta A Mol Biomol Spectrosc. 2010 Sep 1;76(5):446-51. doi: 10.1016/j.saa.2009.12.023. Epub 2009 Dec 16.
The 8-quinolineboronic acid phosphorescent molecular switch (abbreviated as PMS-8-QBA. Thereinto, 8-QBA is 8-quinolineboronic acid, and PMS is phosphorescent molecular switch) was found for the first time. PMS-8-QBA, which was in the "off" state, could only emit weak room temperature phosphorescence (RTP) on the acetyl cellulose membrane (ACM). However, PMS-8-QBA turned "on" automatically for its changed structure, causing that the RTP of 8-QBA in the system increased, after PMS-8-QBA-WGA (WGA is wheat germ agglutinin) was formed by reaction between -OH of PMS-8-QBA and -COOH of WGA. More interesting is that the -NH(2) of PMS-8-QBA-WGA could react with the -COOH of alkaline phosphatase (AP) to form the affinity adsorption (AA) product WGA-AP-WGA-8-QBA-PMS (containing -NH-CO- bond), which caused RTP of the system to greatly increase. Thus, affinity adsorption solid substrate room temperature phosphorimetry using PMS-8-QBA as labelling reagent (PMS-8-QBA-AA-SSRTP) for the determination of trace AP was established. The method had many advantages, such as high sensitivity (the detection limit (LD) was 2.5zgspot(-1). For sample volume of 0.40mulspot(-1), corresponding concentration was 6.2x10(-18)gml(-1)), good selectivity (the allowed concentration of coexisting material was higher, when the relative error was +/-5%), high accuracy (applied to detection of AP content in serum samples, the result was coincided with those obtained by enzyme-linked immunoassay), which was suitable for the detection of trace AP content in serum samples and the forecast of human diseases. Meanwhile, the mechanism of PMS-8-QBA-AASSRTP was discussed. The new field of analytical application and clinic diagnosis technique of molecule switch are exploited, based on the phosphorescence characteristic of PMS-8-QBA, the AA reaction between WGA and AP, as well as the relation between AP content and human diseases. The research results promote the development and interpenetrate among molecule switch technique, lectin science and SSRTP.
首次发现了 8-喹啉硼酸磷光分子开关(简称 PMS-8-QBA,其中 8-QBA 是 8-喹啉硼酸,PMS 是磷光分子开关)。在乙酰纤维素膜(ACM)上,处于“关闭”状态的 PMS-8-QBA 只能发出微弱的室温磷光(RTP)。然而,当 PMS-8-QBA 与 WGA(麦胚凝集素)的-COOH 反应形成 PMS-8-QBA-WGA 后,其结构发生变化而自动“开启”,导致体系中 8-QBA 的 RTP 增加。更有趣的是,PMS-8-QBA-WGA 的-NH(2)可以与碱性磷酸酶(AP)的-COOH 反应,形成亲和吸附(AA)产物 WGA-AP-WGA-8-QBA-PMS(含有-NH-CO-键),这导致体系的 RTP 大大增加。因此,建立了以 PMS-8-QBA 为标记试剂的亲和吸附固底物室温磷光法(PMS-8-QBA-AA-SSRTP)用于痕量 AP 的测定。该方法具有许多优点,例如高灵敏度(检测限(LD)为 2.5zgspot(-1)。对于 0.40mulspot(-1)的样品体积,相应的浓度为 6.2x10(-18)gml(-1)),良好的选择性(允许共存物质的浓度较高,相对误差为 +/-5%),高准确性(用于检测血清样品中的 AP 含量,结果与酶联免疫测定法一致),适用于血清样品中痕量 AP 含量的检测和人类疾病的预测。同时,讨论了 PMS-8-QBA-AASSRTP 的机制。基于 PMS-8-QBA 的磷光特性、WGA 和 AP 之间的 AA 反应以及 AP 含量与人类疾病之间的关系,开拓了分子开关分析应用和临床诊断技术的新领域。研究结果促进了分子开关技术、凝集素科学和 SSRTP 的发展和渗透。