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通过使用定制的纳米粒子来提高酶检测的选择性。

Enhancing the selectivity of enzyme detection by using tailor-made nanoparticles.

出版信息

Anal Chem. 2013 May 21;85(10):4853-7. doi: 10.1021/ac4007914. Epub 2013 May 10.

Abstract

Development of effective ways to specifically and reversibly block the activity of an enzyme is highly desirable for enhancing the selectivity of enzyme assays. Here we demonstrate a novel approach for selective detection of enzyme activities in complex biological samples by using tailor-made nanoparticles. Employing deoxyribonuclease I (DNase I) as a model enzyme template, we prepared surface imprinted polymers over magnetic nanoparticles with monomers screened out of commonly used functional monomers. The resultant Fe3O4@MIP nanoparticles can not only block the activity of the target enzyme via selective adsorption but also quantitatively release the bound enzyme under mild conditions with the assistance of metal ion cofactors, which offers a very useful tool for enhancing the selectivity in enzyme detection. The approach enables sequential detection of the activities of 3'-5' exonuclease and DNase I in cell lysates. The strategy may be further extended to the detection of other enzyme proteins.

摘要

开发有效且可特异性及可逆性地阻断酶活性的方法对于提高酶分析的选择性非常重要。在此,我们展示了一种通过使用定制纳米粒子来选择性检测复杂生物样品中酶活性的新方法。我们以脱氧核糖核酸酶 I(DNase I)为模型酶模板,使用筛选出的常用功能单体制备了磁性纳米粒子表面印迹聚合物。所得的 Fe3O4@MIP 纳米粒子不仅可以通过选择性吸附来阻断目标酶的活性,还可以在金属离子辅因子的帮助下在温和条件下定量释放结合的酶,这为提高酶检测的选择性提供了非常有用的工具。该方法可用于在细胞裂解物中顺序检测 3'-5'核酸外切酶和 DNase I 的活性。该策略可进一步扩展到其他酶蛋白的检测。

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