Screening and isolation of quorum sensing inhibitors of Pseudomonas aeruginosa from Phellodendron amurense extracts using bio-affinity chromatography

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL Journal of separation science Pub Date : 2024-08-02 DOI:10.1002/jssc.202400222
Yu Yi, Ye Zhou, Susu Lin, Kefan Shi, Jianfeng Mei, Guoqing Ying, Shujiang Wu
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Abstract

Drug-resistant bacterial infections pose a significant challenge in the field of bacterial disease treatment. Finding new antibacterial pathways and targets to combat drug-resistant bacteria is crucial. The bacterial quorum sensing (QS) system regulates the expression of bacterial virulence factors. Inhibiting bacterial QS and reducing bacterial virulence can achieve antibacterial therapeutic effects, making QS inhibition an effective strategy to control bacterial pathogenicity. This article mainly focused on the PqsA protein in the QS system of Pseudomonas aeruginosa. An affinity chromatography medium was developed using the SpyTag/SpyCatcher heteropeptide bond system. Berberine, which can interact with the PqsA target, was screened from Phellodendron amurense by affinity chromatography. We characterized its structure, verified its inhibitory activity on P. aeruginosa, and preliminarily analyzed its mechanism using molecular docking technology. This method can also be widely applied to the immobilization of various protein targets and the effective screening of active substances.

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利用生物亲和层析技术从黄柏提取物中筛选和分离铜绿假单胞菌的法定量感应抑制剂。
耐药性细菌感染给细菌疾病治疗领域带来了巨大挑战。寻找新的抗菌途径和靶点来对抗耐药细菌至关重要。细菌的法定量感应(QS)系统调控着细菌毒力因子的表达。抑制细菌QS,降低细菌毒力,可以达到抗菌治疗效果,因此抑制QS是控制细菌致病性的有效策略。本文主要研究铜绿假单胞菌 QS 系统中的 PqsA 蛋白。利用 SpyTag/SpyCatcher 异肽键系统开发了一种亲和层析介质。通过亲和色谱法从黄柏中筛选出了能与 PqsA 目标相互作用的小檗碱。我们确定了其结构特征,验证了其对铜绿假单胞菌的抑制活性,并利用分子对接技术初步分析了其作用机制。该方法还可广泛应用于各种蛋白质靶标的固定化和活性物质的有效筛选。
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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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