Literature DB >> 9511932

Purification, characterization, and expression of CFTR nucleotide-binding domains.

J P Clancy1, Z Bebök, E J Sorscher.   

Abstract

The nucleotide binding domains (NBDs) within CFTR were initially predicted to lie in the cell cytoplasm, and to gate anion permeability through a pore that was present in membrane spanning alpha helices of the overall polypeptide. Our studies designed to characterize CFTR suggest several important features of the isolated nucleotide binding domain. NBD-1 appears to bind nucleotides with similar affinity to the full-length CFTR protein. In solution, the domain contains a high beta sheet content and self-associates into ordered polymers with molecular mass greater than 300,000 Daltons. The domain is very lipophilic, disrupts liposomes, and readily enters the planar lipid bilayer. Clinically important mutations in the domain may disrupt the nucleotide binding capabilities of the protein, either through a direct effect on the nucleotide binding site, or through effects that influence the overall folding of the domain in vitro. Finally, after expression in human epithelial cells (including epithelial cells from a CF patient), the first nucleotide binding domain targets the plasma membrane even in the absence of other constituents of full-length CFTR and mediates anion permeability in these cells.

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Year:  1997        PMID: 9511932     DOI: 10.1023/a:1022487024031

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   3.853


  29 in total

1.  Structural model of the nucleotide-binding conserved component of periplasmic permeases.

Authors:  C S Mimura; S R Holbrook; G F Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

2.  The ATP-binding component of a prokaryotic traffic ATPase is exposed to the periplasmic (external) surface.

Authors:  V Baichwal; D Liu; G F Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1993-01-15       Impact factor: 11.205

3.  Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

Authors:  M Cheung; M H Akabas
Journal:  Biophys J       Date:  1996-06       Impact factor: 4.033

4.  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

5.  Demonstration that CFTR is a chloride channel by alteration of its anion selectivity.

Authors:  M P Anderson; R J Gregory; S Thompson; D W Souza; S Paul; R C Mulligan; A E Smith; M J Welsh
Journal:  Science       Date:  1991-07-12       Impact factor: 47.728

6.  Activation of DeltaF508 CFTR in an epithelial monolayer.

Authors:  Z Bebök; C J Venglarik; Z Pánczél; T Jilling; K L Kirk; E J Sorscher
Journal:  Am J Physiol       Date:  1998-08

7.  Stoichiometry of recombinant cystic fibrosis transmembrane conductance regulator in epithelial cells and its functional reconstitution into cells in vitro.

Authors:  J Marshall; S Fang; L S Ostedgaard; C R O'Riordan; D Ferrara; J F Amara; H Hoppe; R K Scheule; M J Welsh; A E Smith
Journal:  J Biol Chem       Date:  1994-01-28       Impact factor: 5.157

8.  Affinity purification of insoluble recombinant fusion proteins containing glutathione-S-transferase.

Authors:  J Hartman; P Daram; R A Frizzell; T Rado; D J Benos; E J Sorscher
Journal:  Biotechnol Bioeng       Date:  1992-04-05       Impact factor: 4.530

9.  Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator.

Authors:  T P Carroll; M M Morales; S B Fulmer; S S Allen; T R Flotte; G R Cutting; W B Guggino
Journal:  J Biol Chem       Date:  1995-05-19       Impact factor: 5.157

10.  Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway.

Authors:  B H Qu; P J Thomas
Journal:  J Biol Chem       Date:  1996-03-29       Impact factor: 5.157

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