A LecA Ligand Identified from a Galactoside‐Conjugate Array Inhibits Host Cell Invasion by Pseudomonas aeruginosa1. (7th July 2014)

• Record Type: Journal Article
• Authors: Novoa, Alexandre; Eierhoff, Thorsten; Topin, Jérémie; Varrot, Annabelle; Barluenga, Sofia; Imberty, Anne; Römer, Winfried; Winssinger, Nicolas
• Is Part Of: Angewandte Chemie. Volume 126:Number 34(2014)
• Page Start: 9031
• Page End: 9035
• Publication Date: 2014-07-07
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201402831
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Lectin LecA is a virulence factor of Pseudomonas aeruginosa involved in lung injury, mortality, and cellular invasion. Ligands competing with human glycoconjugates for LecA binding are thus promising candidates to counteract P. aeruginosa infections. We have identified a novel divalent ligand from a focused galactoside(Gal)‐conjugate array which binds to LecA with very high affinity (<italic>K</italic>_d=82 n<sc>M</sc>). Crystal structures of LecA complexed with the ligand together with modeling studies confirmed its ability to chelate two binding sites of LecA. The ligand lowers cellular invasiveness of P. aeruginosa up to 90 % when applied in the range of 0.05–5 μ<italic><sc>M</sc></italic>. Hence, this ligand might lead to the development of drugs against P. aeruginosa infection.</p> </abstract>