5JYC

Crystal structure of the E153Q mutant of the CFTR inhibitory factor Cif containing the adducted 14,15-EET hydrolysis intermediate

5JYC の概要

• エントリーDOI: 10.2210/pdb5jyc/pdb
• 分子名称: CFTR inhibitory factor, (5~{Z},11~{Z},14~{R},15~{R})-14,15-bis(oxidanyl)icosa-5,8,11-trienoic acid (3 entities in total)
• 機能のキーワード: epoxide hydrolase, hydroxyalkyl-enzyme intermediate, hydrolase
• 由来する生物種: Pseudomonas aeruginosa (strain UCBPP-PA14)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 138008.79

構造登録者

Hvorecny, K.L.,Madden, D.R. (登録日: 2016-05-13, 公開日: 2017-01-11, 最終更新日: 2024-10-30)

主引用文献

Flitter, B.A.,Hvorecny, K.L.,Ono, E.,Eddens, T.,Yang, J.,Kwak, D.H.,Bahl, C.D.,Hampton, T.H.,Morisseau, C.,Hammock, B.D.,Liu, X.,Lee, J.S.,Kolls, J.K.,Levy, B.D.,Madden, D.R.,Bomberger, J.M.
Pseudomonas aeruginosa sabotages the generation of host proresolving lipid mediators.
Proc. Natl. Acad. Sci. U.S.A., 114:136-141, 2017

PubMed Abstract: Recurrent Pseudomonas aeruginosa infections coupled with robust, damaging neutrophilic inflammation characterize the chronic lung disease cystic fibrosis (CF). The proresolving lipid mediator, 15-epi lipoxin A (15-epi LXA), plays a critical role in limiting neutrophil activation and tissue inflammation, thus promoting the return to tissue homeostasis. Here, we show that a secreted P. aeruginosa epoxide hydrolase, cystic fibrosis transmembrane conductance regulator inhibitory factor (Cif), can disrupt 15-epi LXA transcellular biosynthesis and function. In the airway, 15-epi LXA production is stimulated by the epithelial-derived eicosanoid 14,15-epoxyeicosatrienoic acid (14,15-EET). Cif sabotages the production of 15-epi LXA by rapidly hydrolyzing 14,15-EET into its cognate diol, eliminating a proresolving signal that potently suppresses IL-8-driven neutrophil transepithelial migration in vitro. Retrospective analyses of samples from patients with CF supported the translational relevance of these preclinical findings. Elevated levels of Cif in bronchoalveolar lavage fluid were correlated with lower levels of 15-epi LXA, increased IL-8 concentrations, and impaired lung function. Together, these findings provide structural, biochemical, and immunological evidence that the bacterial epoxide hydrolase Cif disrupts resolution pathways during bacterial lung infections. The data also suggest that Cif contributes to sustained pulmonary inflammation and associated loss of lung function in patients with CF.

PubMed: 27980032
DOI: 10.1073/pnas.1610242114

実験手法

X-RAY DIFFRACTION (2 Å)