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CUPRA-ZYME:一种用于测量碳水化合物活性酶活性、途径和底物特异性的分析方法。

CUPRA-ZYME: An Assay for Measuring Carbohydrate-Active Enzyme Activities, Pathways, and Substrate Specificities.

机构信息

Department of Chemistry , University of Alberta , Edmonton , Alberta , Canada T6G 2G2.

Complex Carbohydrate Research Center , University of Georgia , Athens , Georgia 30602 , United States.

出版信息

Anal Chem. 2020 Feb 18;92(4):3228-3236. doi: 10.1021/acs.analchem.9b05007. Epub 2020 Feb 7.

Abstract

Carbohydrate-Active enZymes (CAZymes) are involved in the synthesis, degradation, and modification of carbohydrates. They play critical roles in diverse physiological and pathophysiological processes, have important industrial and biotechnological applications, are important drug targets, and represent promising biomarkers for the diagnosis of a variety of diseases. Measurements of their activities, catalytic pathway, and substrate specificities are essential to a comprehensive understanding of the biological functions of CAZymes and exploiting these enzymes for industrial and biomedical applications. For glycosyl hydrolases a variety of sensitive and quantitative spectrophotometric techniques are available. However, measuring the activity of glycosyltransferases is considerably more challenging. Here, we introduce CUPRA-ZYME, a versatile and quantitative electrospray ionization mass spectrometry (ESI-MS) assay for measuring the kinetic parameters of CAZymes, monitoring reaction pathways, and profiling substrate specificities. The method employs the recently developed competitive universal proxy receptor assay (CUPRA), implemented in a time-resolved manner. Measurements of the hydrolysis kinetics of CUPRA substrates containing ganglioside oligosaccharides by the glycosyl hydrolase human neuraminidase 3 served to validate the reliability of kinetic parameters measured by CUPRA-ZYME and highlight its use in establishing catalytic pathways. Applications to libraries of substrates demonstrate the potential of the assay for quantitative profiling of the substrate specificities glycosidases and glycosyltransferases. Finally, we show how the comparison of the reactivity of CUPRA substrates and glycan substrates present on glycoproteins, measured simultaneously, affords a unique opportunity to quantitatively study how the structure and protein environment of natural glycoconjugate substrates influences CAZyme activity.

摘要

碳水化合物活性酶(CAZymes)参与碳水化合物的合成、降解和修饰。它们在多种生理和病理生理过程中发挥着关键作用,具有重要的工业和生物技术应用价值,是重要的药物靶点,并且代表了用于诊断各种疾病的有前途的生物标志物。对它们的活性、催化途径和底物特异性的测量对于全面了解 CAZymes 的生物学功能以及为工业和生物医学应用开发这些酶至关重要。对于糖基水解酶,有多种灵敏和定量的分光光度技术可用。然而,测量糖基转移酶的活性具有相当大的挑战性。在这里,我们引入了 CUPRA-ZYME,这是一种通用且定量的电喷雾电离质谱(ESI-MS)测定法,用于测量 CAZymes 的动力学参数、监测反应途径和分析底物特异性。该方法采用了最近开发的竞争性通用代理受体测定法(CUPRA),以时间分辨的方式实施。通过糖苷水解酶人神经氨酸酶 3对含有神经节苷脂寡糖的 CUPRA 底物的水解动力学的测量,验证了通过 CUPRA-ZYME 测量的动力学参数的可靠性,并突出了其在建立催化途径中的用途。对底物文库的应用证明了该测定法用于定量分析糖苷酶和糖基转移酶底物特异性的潜力。最后,我们展示了如何通过同时测量 CUPRA 底物和糖蛋白上存在的聚糖底物的反应性,为定量研究天然糖缀合物底物的结构和蛋白质环境如何影响 CAZyme 活性提供了独特的机会。

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