Literature DB >> 11804193

Cystic fibrosis: a brief look at some highlights of a decade of research focused on elucidating and correcting the molecular basis of the disease.

Y H Ko1, P L Pedersen.   

Abstract

The disease Cystic Fibrosis (CF) is caused by mutations in the protein called CFTR, cystic fibrosis transmembrane conductance regulator, an ABC-transporter-like protein found in the plasma membrane of animal cells. CFTR is believed to function primarily as a Cl- channel, but evidence is mounting that this protein has other roles as well. Structurally, CFTR consists of a single polypeptide chain (1480 amino acids) that folds into 5 distinct domains. These include 2 transmembrane domains that are involved in channel formation; 2 nucleotide-binding domains (NBF1 and NBF2), the first of which clearly binds and hydrolyzes ATP; and 1 regulatory domain (R) that is phosphorylated in a cAMP-dependent process. Currently, the 3D structure of neither CFTR nor its domains has been elucidated, although both nucleotide domains have been modeled in 3D, and solution structures in 3D have been obtained for peptide segments of NBF1. The most common mutation causing CF is the deletion (delta) of a single phenylalanine (F) in position 508 within a putative helix located in NBF1. CF patients bearing this deltaF508 mutation frequently experience chronic lung infections, particularly by Pseudomonas aeruginosa, and have a life span that rarely exceeds the age of 30. Since the CFTR gene was cloned and sequenced in 1989, there has been over a decade of research focused on understanding the molecular basis of CF caused by the deltaF508 mutation, with the ultimate objective of using the knowledge gained to carry out additional research designed to correct the underlying defect. In general, this pioneering or "ground roots" research has succeeded according to plan. This brief review summarizes some of the highlights with a focus on those studies conducted in the authors' laboratory. For us, this research has been both exciting and rewarding mainly because the results obtained, despite very limited funding, have provided considerable insight, not only into the chemical, molecular, and pathogenic basis of CF, but have made it possible for us and others to now develop novel, chemically rational, and "cost effective" strategies to identify agents that correct the structural defect in the deltaF508 CFTR protein causing most cases of CF.

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Year:  2001        PMID: 11804193     DOI: 10.1023/a:1012831322753

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  70 in total

1.  The crystal structure of the MJ0796 ATP-binding cassette. Implications for the structural consequences of ATP hydrolysis in the active site of an ABC transporter.

Authors:  Y R Yuan; S Blecker; O Martsinkevich; L Millen; P J Thomas; J F Hunt
Journal:  J Biol Chem       Date:  2001-06-11       Impact factor: 5.157

2.  Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

Authors:  W Dalemans; P Barbry; G Champigny; S Jallat; K Dott; D Dreyer; R G Crystal; A Pavirani; J P Lecocq; M Lazdunski
Journal:  Nature       Date:  1991 Dec 19-26       Impact factor: 49.962

3.  Cystic fibrosis transmembrane conductance regulator: the purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region.

Authors:  N T Lu; P L Pedersen
Journal:  Arch Biochem Biophys       Date:  2000-03-01       Impact factor: 4.013

4.  A recombinant polypeptide model of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase.

Authors:  C Randak; P Neth; E A Auerswald; C Eckerskorn; I Assfalg-Machleidt; W Machleidt
Journal:  FEBS Lett       Date:  1997-06-30       Impact factor: 4.124

5.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

6.  Phosphorylation-regulated Cl- channel in CHO cells stably expressing the cystic fibrosis gene.

Authors:  J A Tabcharani; X B Chang; J R Riordan; J W Hanrahan
Journal:  Nature       Date:  1991-08-15       Impact factor: 49.962

7.  Modeling of nucleotide binding domains of ABC transporter proteins based on a F1-ATPase/recA topology: structural model of the nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator (CFTR).

Authors:  M A Bianchet; Y H Ko; L M Amzel; P L Pedersen
Journal:  J Bioenerg Biomembr       Date:  1997-10       Impact factor: 2.945

Review 8.  Altered protein folding may be the molecular basis of most cases of cystic fibrosis.

Authors:  P J Thomas; Y H Ko; P L Pedersen
Journal:  FEBS Lett       Date:  1992-11-02       Impact factor: 4.124

9.  Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator.

Authors:  M H Akabas; C Kaufmann; T A Cook; P Archdeacon
Journal:  J Biol Chem       Date:  1994-05-27       Impact factor: 5.157

10.  The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity.

Authors:  M R Carson; S M Travis; M J Welsh
Journal:  J Biol Chem       Date:  1995-01-27       Impact factor: 5.157

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  9 in total

Review 1.  Transport ATPases in biological systems and relationship to human disease: a brief overview.

Authors:  Peter L Pedersen
Journal:  J Bioenerg Biomembr       Date:  2002-10       Impact factor: 2.945

2.  Muscarinic receptor stimulation activates a Ca(2+)-dependent Cl(-) conductance in rat distal colon.

Authors:  G Schultheiss; A Siefjediers; M Diener
Journal:  J Membr Biol       Date:  2005-04       Impact factor: 1.843

3.  Co-culture models of Pseudomonas aeruginosa biofilms grown on live human airway cells.

Authors:  Sophie Moreau-Marquis; Carly V Redelman; Bruce A Stanton; Gregory G Anderson
Journal:  J Vis Exp       Date:  2010-10-06       Impact factor: 1.355

4.  Analysis of ABCC6 (MRP6) in normal human tissues.

Authors:  Konstanze Beck; Kimiko Hayashi; Ka'ohimanu Dang; Masando Hayashi; Charles D Boyd
Journal:  Histochem Cell Biol       Date:  2005-05-12       Impact factor: 4.304

5.  The Pseudomonas aeruginosa magnesium transporter MgtE inhibits transcription of the type III secretion system.

Authors:  Gregory G Anderson; Timothy L Yahr; Rustin R Lovewell; George A O'Toole
Journal:  Infect Immun       Date:  2009-12-22       Impact factor: 3.441

6.  Epoxide-mediated CifR repression of cif gene expression utilizes two binding sites in Pseudomonas aeruginosa.

Authors:  Alicia E Ballok; Christopher D Bahl; Emily L Dolben; Allia K Lindsay; Jessica D St Laurent; Deborah A Hogan; Dean R Madden; George A O'Toole
Journal:  J Bacteriol       Date:  2012-07-27       Impact factor: 3.490

7.  In vitro analysis of tobramycin-treated Pseudomonas aeruginosa biofilms on cystic fibrosis-derived airway epithelial cells.

Authors:  Gregory G Anderson; Sophie Moreau-Marquis; Bruce A Stanton; George A O'Toole
Journal:  Infect Immun       Date:  2008-01-22       Impact factor: 3.441

8.  Cystic fibrosis transmembrane conductance regulator: the NBF1+R (nucleotide-binding fold 1 and regulatory domain) segment acting alone catalyses a Co2+/Mn2+/Mg2+-ATPase activity markedly inhibited by both Cd2+ and the transition-state analogue orthovanadate.

Authors:  Jean Philippe Annereau; Young Hee Ko; Peter L Pedersen
Journal:  Biochem J       Date:  2003-04-15       Impact factor: 3.857

9.  The PEST sequence does not contribute to the stability of the cystic fibrosis transmembrane conductance regulator.

Authors:  Eva Y Chen; David M Clarke
Journal:  BMC Biochem       Date:  2002-10-02       Impact factor: 4.059

  9 in total

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