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一种用于β-内酰胺酶检测的自固定化荧光探针。

A Self-Immobilizing and Fluorogenic Probe for β-Lactamase Detection.

作者信息

Mao Wuyu, Xia Lingying, Wang Yaqun, Xie Hexin

机构信息

State Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, P.R. China.

出版信息

Chem Asian J. 2016 Dec 19;11(24):3493-3497. doi: 10.1002/asia.201601344. Epub 2016 Nov 16.

Abstract

The spread of antibiotic resistance in pathogenic bacteria has become one of the major concerns to public health. Improved monitoring of drug resistance is of high importance for infectious disease control. One of the major mechanisms for bacteria to overcome treatment of antibiotics is the production of β-lactamases, which are enzymes that hydrolyze the β-lactam ring of the antibiotic. In this study, we have developed a self-immobilizing and fluorogenic probe for the detection of β-lactamase activity. This fluorogenic reagent, upon activation by β-lactamases, turns on a fluorescence signal and, more importantly, generates a covalent linkage to the target enzymes or the nearby proteins. The covalent labeling of enzymes was confirmed by SDS-PAGE analysis and MALDI-TOF mass spectrometry. The utility of this structurally simple probe was further confirmed by the fluorescent labeling of a range of β-lactamase-expressing bacteria.

摘要

病原菌中抗生素耐药性的传播已成为公共卫生的主要关注问题之一。加强耐药性监测对于传染病控制至关重要。细菌克服抗生素治疗的主要机制之一是产生β-内酰胺酶,β-内酰胺酶是一种能水解抗生素β-内酰胺环的酶。在本研究中,我们开发了一种用于检测β-内酰胺酶活性的自固定荧光探针。这种荧光试剂在被β-内酰胺酶激活后会开启荧光信号,更重要的是,会与目标酶或附近的蛋白质形成共价连接。通过SDS-PAGE分析和MALDI-TOF质谱法证实了酶的共价标记。一系列表达β-内酰胺酶的细菌的荧光标记进一步证实了这种结构简单的探针的实用性。

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