School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, 710061, China; Shaanxi Engineering Research Center of Cardiovascular Drugs Screening & Analysis, Xi'an, 710061, China.
Australian Centre for Research on Separation Science (ACROSS), School of Natural Sciences, University of Tasmania, Hobart, 7001, Australia.
Anal Chim Acta. 2022 May 29;1209:339875. doi: 10.1016/j.aca.2022.339875. Epub 2022 Apr 27.
The enrichment of glycoproteins by fluorescence molecular imprinting has shown an attractive application prospect, however, its specificity and sensitivity in actual sample analysis remain a significant challenge. In this work, a novel fluorescent molecular imprinted nanoplatform (MMIPs@QDs) was constructed for the efficient recognition and determination of glycoproteins by combining the glycopeptide template and the post-imprinting modification of nitrogen-doped graphene quantum dots. The synthetic MMIPs@QDs exhibited high adsorption capacity and rapid binding kinetics. Satisfying selectivity and sensitivity were obtained using MMIPs@QDs, with an imprinting factor of 7.71 and a limit of detection of 0.20 μg mL, respectively. The efficiency and applicability of this proposed method were validated by the detection of ovalbumin in egg white samples, showed high recoveries (94.3%-100.2%) and acceptable relative standard deviation (1.79%-7.36%). This fluorescent molecular imprinted nanoplatform provides a new approach to address the limitations of existing protein detection techniques.
糖蛋白的荧光分子印迹富集显示出了诱人的应用前景,然而,其在实际样品分析中的特异性和灵敏度仍然是一个重大挑战。在这项工作中,通过将糖肽模板与氮掺杂石墨烯量子点的后印迹修饰相结合,构建了一种新型荧光分子印迹纳米平台(MMIPs@QDs),用于糖蛋白的高效识别和测定。所合成的 MMIPs@QDs 表现出高吸附容量和快速结合动力学。使用 MMIPs@QDs 获得了令人满意的选择性和灵敏度,分别为 7.71 的印迹因子和 0.20μg mL 的检测限。通过对蛋清样品中卵清白蛋白的检测,验证了该方法的效率和适用性,显示出高回收率(94.3%-100.2%)和可接受的相对标准偏差(1.79%-7.36%)。这种荧光分子印迹纳米平台为解决现有蛋白质检测技术的局限性提供了一种新方法。