CFTR inhibitory factor

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Ribbon diagram of the Cif dimer from P. aeruginosa PA14. From PDB 3KD2.

The CFTR inhibitory factor (Cif) is a protein virulence factor secreted by the Gram-negative bacterium Pseudomonas aeruginosa.[1] Discovered at Dartmouth Medical School, Cif is able to alter the trafficking of select ABC transporters in eukaryotic epithelial cells, such as the cystic fibrosis transmembrane conductance regulator (CFTR),[1] and P-glycoprotein[2] by interfering with the host deubiquitinating machinery.[3] By promoting the ubiquitin-mediated degradation of CFTR, Cif is able to phenocopy cystic fibrosis at the cellular level.[1][4] The cif gene is transcribed as part of a 3 gene operon, whose expression is negatively regulated by CifR, a TetR family repressor.[5]

Cellular mechanism of action[edit]

Cif was first discovered by co-culturing P. aeruginosa with human airway epithelial cells and monitoring the resulting effect on chloride ion efflux across a polarized monolayer. After co-culture, the CFTR specific chloride ion efflux was found to be drastically reduced.[4] This was determined to be caused by reduced levels of CFTR at the apical surface of these cells. This effect was later found to be the result of a single secreted protein produced by P. aeruginosa, which was named the CFTR inhibitory factor for this initial phenotype. Cif is secreted by P. aeruginosa PA14 as soluble protein as well as packaged into outer membrane vesicles (OMV).[6] Cif is far more potent when applied in OMVs, likely due to efficiency of delivery. Purified, recombinant Cif protein can be applied to polarized monolayers of mammalian cells and promote the removal of CFTR[1][7] and P-glycoprotein[2] from the apical membrane. Cif accomplishes this by interfering with the host deubiquitylation system.[3]

Epoxide hydrolase enzyme mechanism[edit]

The active site of Cif is shown with a Cα trace in gray, and side chains of select residues playing a role in catalysis are displayed as sticks. From PDB 3KD2.

Cif is an epoxide hydrolase (EH) with unique substrate selectivity.[7] Cif is the first example of an EH serving as a virulence factor. Based on structural comparison, it appears that the enzyme utilizes a catalytic triad of residues Asp129, Glu153 and His297, with accessory residues His177 and Tyr239 coordinating the epoxide oxygen during ring opening. Cif is also the first example of an EH utilizing a His-Tyr pair to coordinate an epoxide substrate, rather than the canonical Tyr-Tyr pair.[8] In the proposed enzyme mechanism, Asp129 nucleophilically attacks a carbon of the epoxide moiety of a substrate, forming an ester linked enzyme-acyl intermediate. The preference for which carbon is attacked varies depending upon the substrate. In the second step of the reaction, a water molecule is activated by the charge-relay His297-Glu153 pair, and undergoes nucleophilic attack on the Cγ of Asp129. This hydrolyzes the ester group, liberating the hydrolysis product as a vicinal diol.[7]

Structure[edit]

Cif belongs to the α/β hydrolase family of proteins. Its structure was determined by X-ray crystallography and consists of the canonical α/β hydrolase fold with a cap domain, which it uses to constitutively homo-dimerize in solution. The active site is burred in the interior of the protein at the interface between the α/β hydrolase core and the cap.[7][9]

References[edit]

  1. ^ a b c d MacEachran DP, Ye S, Bomberger JM, Hogan DA, Swiatecka-Urban A, Stanton BA, O'Toole GA. (2007). "The Pseudomonas aeruginosa Secreted Protein PA2934 Decreases Apical Membrane Expression of the Cystic Fibrosis Transmembrane Conductance Regulator". Infect Immun 75 (8): 3902–3912. doi:10.1128/IAI.00338-07. PMC 1951978. PMID 17502391. 
  2. ^ a b Ye S, MacEachran DP, Hamilton JW, O'Toole GA, Stanton BA. (2008). "Chemotoxicity of doxorubicin and surface expression of P-glycoprotein (MDR1) is regulated by the Pseudomonas aeruginosa toxin Cif". Am J Physiol Cell Physiol 295 (3): C807–18. doi:10.1152/ajpcell.00234.2008. PMC 2544439. PMID 18650266. 
  3. ^ a b Bomberger JM, Ye S, Maceachran DP, Koeppen K, Barnaby RL, O'Toole GA, Stanton BA. (2011). "A Pseudomonas aeruginosa toxin that hijacks the host ubiquitin proteolytic system". In Rohde, John. PLoS Pathog 7 (3): e1001325. doi:10.1371/journal.ppat.1001325. PMC 3063759. PMID 21455491. 
  4. ^ a b Swiatecka-Urban A, Moreau-Marquis S, Maceachran DP, Connolly JP, Stanton CR, Su JR, Barnaby R, O'toole GA, Stanton BA. (2006). "Pseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cells". Am J Physiol Cell Physiol 290 (3): C862–72. doi:10.1152/ajpcell.00108.2005. PMID 16236828. 
  5. ^ MacEachran DP, Stanton BA, O'Toole GA. (2008). "Cif is negatively regulated by the TetR family repressor CifR". J Bacteriol 76 (7): 3197–3206. doi:10.1128/IAI.00305-08. PMC 2446692. PMID 18458065. 
  6. ^ Bomberger JM, Maceachran DP, Coutermarsh BA, Ye S, O'Toole GA, Stanton BA. (2009). "Long-distance delivery of bacterial virulence factors by Pseudomonas aeruginosa outer membrane vesicles". In Ausubel, Frederick M. PLoS Pathog 5 (4): e1000382. doi:10.1371/journal.ppat.1000382. PMC 2661024. PMID 19360133. 
  7. ^ a b c d Bahl CD, Morisseau C, Bomberger JM, Stanton BA, Hammock BD, O'Toole GA, Madden DR. (2010). "Crystal structure of the cystic fibrosis transmembrane conductance regulator inhibitory factor Cif reveals novel active-site features of an epoxide hydrolase virulence factor". J Bacteriol 192 (7): 1785–1795. doi:10.1128/JB.01348-09. PMC 2838060. PMID 20118260. 
  8. ^ Bahl CD, Madden DR. (2012). "Pseudomonas aeruginosa Cif Defines a Distinct Class of α/β Epoxide Hydrolases Utilizing a His/Tyr Ring-opening Pair". Protein Pept Lett 19 (2): 186–193. PMC 3320240. PMID 21933119. 
  9. ^ Bahl CD, MacEachran DP, O'Toole GA, Madden DR. (2010). "Purification, crystallization and preliminary X-ray diffraction analysis of Cif, a virulence factor secreted by Pseudomonas aeruginosa". Acta Crystallogr F66 (1): 26–28. doi:10.1107/S1744309109047599. PMC 2805529. PMID 20057063.