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基于功能化金纳米粒子的简单实时比色法检测糖苷酶活性及其抑制剂筛选应用。

Simple and real-time colorimetric assay for glycosidases activity using functionalized gold nanoparticles and its application for inhibitor screening.

机构信息

Division of Advanced Science and Biotechnology, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Osaka 565-0871, Japan.

出版信息

Anal Chem. 2012 Nov 6;84(21):9089-95. doi: 10.1021/ac301677v. Epub 2012 Oct 9.

Abstract

The development of real-time assays for enzymes has been receiving a great deal of attention in biomedical research recently. Self-immolative elimination is the spontaneous and irreversible disassembly of a multicomponent construct into its constituent fragments through a cascade of elimination processes, in response to external stimuli. Here, we report a simple and real-time colorimetric assay for glycosidases (β-galactosidase and β-glucosidase). Self-immolative elimination was utilized to release amines to give rise to aggregation and color change by electrostatic attraction after cleavage of the trigger by enzymes displayed on functionalized gold nanoparticles (Gal-Lip-AuNPs and Glc-Lip-AuNPs, where AuNPs denotes gold nanoparticles). The detection limits for β-galactosidase and β-glucosidase were as low as 9.2 and 22.3 nM at 20 min, and they improved slightly over time. Thus, glycosidase activity was detected successfully in real time, and this technique could be used for glycosidase inhibitor screening, based on real-time colorimetric variation.

摘要

近年来,实时分析酶的方法在生物医学研究中受到了极大的关注。自焚消除是一种多组分结构通过一系列消除过程自发且不可逆地分解为其组成片段的过程,以响应外部刺激。在这里,我们报道了一种用于糖苷酶(β-半乳糖苷酶和β-葡萄糖苷酶)的简单实时比色分析方法。利用自焚消除来释放胺,通过酶在功能化金纳米粒子(Gal-Lip-AuNPs 和 Glc-Lip-AuNPs,其中 AuNPs 表示金纳米粒子)上显示的触发物被切割后,通过静电力吸引引起聚集和颜色变化。β-半乳糖苷酶和β-葡萄糖苷酶的检测限在 20 分钟时低至 9.2 和 22.3 nM,并且随着时间的推移略有提高。因此,成功地实时检测了糖苷酶的活性,并且可以基于实时比色变化来筛选糖苷酶抑制剂。

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