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蛋白水解介导的金纳米粒子保护及其用于肽酶灵敏活性分析。

Proteolysis-mediated protection of gold nanoparticles for sensitive activity assay of peptidases.

机构信息

State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.

出版信息

Talanta. 2013 Mar 30;107:233-8. doi: 10.1016/j.talanta.2013.01.016. Epub 2013 Jan 17.

Abstract

Rapid, sensitive and quantitative assays for peptide hydrolysis enzymes are of paramount importance for drug development and in the diagnosis of disease. Here, we proposed a novel biosensor for sensitive and selective active screening of peptidases. This strategy relies on the proteolysis-mediated protection of gold nanoparticles (AuNPs) that were decorated with biotin-labeled substrate peptides and can be aggregated by streptavidin. Enzyme-mediated protection of AuNPs offers this strategy high specificity, and the use of AuNPs additionally allows a visual and homogeneous assay format, thus permitting improved simplicity and throughput of the assays. As a model case, desirable selectivity and sensitivity in peptidase assay were achieved in the active assays of pancreatic elastase with a wide linear response range from 0.005 to 0.10 U/mL and a detection limit of 0.003 U/mL. The results indicated that this strategy can offer a simple, robust and convenient platform for visualized peptidase activity analysis and related biochemical studies with high sensitivity and selectivity.

摘要

用于肽水解酶的快速、灵敏和定量分析对于药物开发和疾病诊断至关重要。在这里,我们提出了一种用于灵敏和选择性活性筛选肽酶的新型生物传感器。该策略依赖于蛋白水解介导的保护金纳米粒子(AuNPs),这些 AuNPs 被生物素标记的底物肽修饰,并可以通过链霉亲和素聚集。酶介导的 AuNPs 保护提供了这种策略的高特异性,并且 AuNPs 的使用还允许进行可视化和均匀的测定格式,从而提高了测定的简单性和通量。作为一个模型案例,在胰腺弹性蛋白酶的活性测定中实现了理想的选择性和灵敏度,线性响应范围从 0.005 到 0.10 U/mL,检测限为 0.003 U/mL。结果表明,该策略可为可视化肽酶活性分析和相关生化研究提供一种简单、稳健和方便的平台,具有高灵敏度和选择性。

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