Discovery of potent 1,1-diarylthiogalactoside glycomimetic inhibitors of Pseudomonas aeruginosa LecA with antibiofilm properties

被引:2
|
作者
Bruneau, Alexandre [1 ]
Gillon, Emilie [2 ]
Brachet, Etienne [1 ]
Alami, Mouad [1 ]
Roques, Christine [3 ]
Varrot, Annabelle [2 ]
Imberty, Anne [2 ]
Messaoudi, Samir [1 ]
机构
[1] Univ Paris Saclay, Univ Paris Sud, BioCIS, CNRS, Chatenay Malabry, France
[2] Univ Grenoble Alpes, CNRS, CERMAV, F-38000 Grenoble, France
[3] Univ Toulouse, Dept Bioprocedes & Syst Microbiens, Lab Genie Chim UMR 5503, CNRS,INPT,UPS,LCG, Toulouse, France
关键词
Thiogalactoside; Pseudomonas aeruginosa; Antibiofilm activity; Structure-activity relationship; DIVALENT INHIBITORS; STRUCTURAL BASIS; LECTIN LECA; PA-IL; BINDING; ALKENYLATION; ALKYNYLATION; SOFTWARE; GROWTH;
D O I
10.1016/j.ejmech.2022.115025
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this work, beta-thiogalactoside mimetics bearing 1,1-diarylmethylene or benzophenone aglycons have been prepared and assayed for their affinity towards LecA, a lectin and virulence factor from Pseudomonas aeruginosa involved in bacterial adhesion and biofilm formation. The hit compound presents higher efficiency than previously described monovalent inhibitors and the crystal structure confirmed the occurrence of additional contacts between the aglycone and the protein surface. The highest affinity (160 nM) was obtained for a divalent ligand containing two galactosides. The monovalent high affinity compound (Kd = 1 mu M) obtained through structureactivity relationship (SAR) showed efficient antibiofilm activity with no associated bactericidal activity.
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页数:12
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