4YW7

Structural Insight into Divalent Galactoside Binding to Pseudomonas aeruginosa lectin LecA

4YW7 の概要

• エントリーDOI: 10.2210/pdb4yw7/pdb
• 分子名称: PA-I galactophilic lectin, CALCIUM ION, beta-D-galactopyranose, ... (5 entities in total)
• 機能のキーワード: galactosides, lectins, sugar binding protein
• 由来する生物種: Pseudomonas aeruginosa
• タンパク質・核酸の鎖数: 16
• 化学式量合計: 209423.47

構造登録者

Visini, R.,Jin, X.,Michaud, G.,Bergmann, M.,Gillon, E.,Imberty, A.,Stocker, A.,Darbre, T.,Pieters, R.,Reymond, J.-L. (登録日: 2015-03-20, 公開日: 2015-09-09, 最終更新日: 2024-05-01)

主引用文献

Visini, R.,Jin, X.,Bergmann, M.,Michaud, G.,Pertici, F.,Fu, O.,Pukin, A.,Branson, T.R.,Thies-Weesie, D.M.,Kemmink, J.,Gillon, E.,Imberty, A.,Stocker, A.,Darbre, T.,Pieters, R.J.,Reymond, J.L.
Structural Insight into Multivalent Galactoside Binding to Pseudomonas aeruginosa Lectin LecA.
Acs Chem.Biol., 10:2455-2462, 2015

PubMed Abstract: Multivalent galactosides inhibiting Pseudomonas aeruginosa biofilms may help control this problematic pathogen. To understand the binding mode of tetravalent glycopeptide dendrimer GalAG2 [(Gal-β-OC6H4CO-Lys-Pro-Leu)4(Lys-Phe-Lys-Ile)2Lys-His-Ile-NH2] to its target lectin LecA, crystal structures of LecA complexes with divalent analog GalAG1 [(Gal-β-OC6H4CO-Lys-Pro-Leu)2Lys-Phe-Lys-Ile-NH2] and related glucose-triazole linked bis-galactosides 3u3 [Gal-β-O(CH2)n-(C2HN3)-4-Glc-β-(C2HN3)-[β-Glc-4-(N3HC2)]2-(CH2)n-O-β-Gal (n = 1)] and 5u3 (n = 3) were obtained, revealing a chelate bound 3u3, cross-linked 5u3, and monovalently bound GalAG1. Nevertheless, a chelate bound model better explaining their strong LecA binding and the absence of lectin aggregation was obtained by modeling for all three ligands. A model of the chelate bound GalAG2·LecA complex was also obtained rationalizing its unusually tight LecA binding (KD = 2.5 nM) and aggregation by lectin cross-linking. The very weak biofilm inhibition with divalent LecA inhibitors suggests that lectin aggregation is necessary for biofilm inhibition by GalAG2, pointing to multivalent glycoclusters as a unique opportunity to control P. aeruginosa biofilms.

PubMed: 26295304
DOI: 10.1021/acschembio.5b00302

実験手法

X-RAY DIFFRACTION (1.82 Å)