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克服铜绿假单胞菌 PqsR 拮抗剂的意外功能反转:一种针对群体感应 pqs 的体内有效抗毒剂。

Overcoming the unexpected functional inversion of a PqsR antagonist in Pseudomonas aeruginosa: an in vivo potent antivirulence agent targeting pqs quorum sensing.

机构信息

Helmholtz-Institute for Pharmaceutical Research Saarland & Pharmaceutical and Medicinal Chemistry, Saarland University, Campus C2.3, 66123 Saarbrücken (Germany).

出版信息

Angew Chem Int Ed Engl. 2014 Jan 20;53(4):1109-12. doi: 10.1002/anie.201307547. Epub 2013 Dec 11.

Abstract

The virulence regulator PqsR of Pseudomonas aeruginosa is considered as an attractive target for attenuating the bacterial pathogenicity without eliciting resistance. However, despite efforts and desires, no promising PqsR antagonist has been discovered thus far. Now, a surprising functionality change of a highly affine PqsR antagonist in P. aeruginosa is revealed, which is mediated by a bacterial signal molecule synthase and responsible for low cellular potency. Blockade of the susceptible position led to the discovery of the first antivirulence compound that is potent in vivo and targets PqsR, thus providing a proof of concept for this novel antivirulence therapy.

摘要

铜绿假单胞菌的毒力调节剂 PqsR 被认为是一种有吸引力的目标,可以减弱细菌的致病性而不引起耐药性。然而,尽管付出了努力和愿望,迄今为止还没有发现有前途的 PqsR 拮抗剂。现在,揭示了铜绿假单胞菌中一种高亲和力 PqsR 拮抗剂的惊人功能变化,这种变化是由细菌信号分子合成酶介导的,并导致细胞内效力降低。阻断易感位置导致发现了第一种有效的体内抗病毒化合物,该化合物针对 PqsR,从而为这种新型抗病毒治疗提供了概念验证。

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