Literature DB >> 9922376

CFTR: mechanism of anion conduction.

D C Dawson1, S S Smith, M K Mansoura.   

Abstract

CFTR: Mechanism of Anion Conduction. Physiol. Rev. 79, Suppl.: S47-S75, 1999. - The purpose of this review is to collect together the results of recent investigations of anion conductance by the cystic fibrosis transmembrane conductance regulator along with some of the basic background that is a prerequisite for developing some physical picture of the conduction process. The review begins with an introduction to the concepts of permeability and conductance and the Nernst-Planck and rate theory models that are used to interpret these parameters. Some of the physical forces that impinge on anion conductance are considered in the context of permeability selectivity and anion binding to proteins. Probes of the conduction process are considered, particularly permeant anions that bind tightly within the pore and block anion flow. Finally, structure-function studies are reviewed in the context of some predictions for the origin of pore properties.

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Year:  1999        PMID: 9922376     DOI: 10.1152/physrev.1999.79.1.S47

Source DB:  PubMed          Journal:  Physiol Rev        ISSN: 0031-9333            Impact factor:   37.312


  42 in total

1.  A novel CFTR disease-associated mutation causes addition of an extra N-linked oligosaccharide.

Authors:  M M Hämmerle; A A Aleksandrov; X B Chang; J R Riordan
Journal:  Glycoconj J       Date:  2000-11       Impact factor: 2.916

2.  Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore.

Authors:  Xiandi Gong; Susan M Burbridge; Elizabeth A Cowley; Paul Linsdell
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

3.  Anion permeation in Ca(2+)-activated Cl(-) channels.

Authors:  Z Qu; H C Hartzell
Journal:  J Gen Physiol       Date:  2000-12       Impact factor: 4.086

4.  Permeant anions control gating of calcium-dependent chloride channels.

Authors:  P Perez-Cornejo; J A De Santiago; J Arreola
Journal:  J Membr Biol       Date:  2004-04-01       Impact factor: 1.843

5.  A combined experimental and quantum chemical study on the putative protonophoric activity of thiocyanate.

Authors:  Peter Schönfeld; Luis Montero; Jürgen Fabian
Journal:  Biophys J       Date:  2005-06-24       Impact factor: 4.033

6.  Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore.

Authors:  P Linsdell; A Evagelidis; J W Hanrahan
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

7.  CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes.

Authors:  G Nagel; P Barbry; H Chabot; E Brochiero; K Hartung; R Grygorczyk
Journal:  J Physiol       Date:  2005-03-03       Impact factor: 5.182

8.  Enteric oxalate secretion is not directly mediated by the human CFTR chloride channel.

Authors:  Robert W Freel; Marguerite Hatch
Journal:  Urol Res       Date:  2008-06-18

9.  Hypertonic saline increases lung epithelial lining fluid glutathione and thiocyanate: two protective CFTR-dependent thiols against oxidative injury.

Authors:  Neal S Gould; Steve Gauthier; Chirag T Kariya; Elysia Min; Jie Huang; Day J Brian
Journal:  Respir Res       Date:  2010-08-27

10.  On the mechanism of CFTR inhibition by a thiazolidinone derivative.

Authors:  Zoia Kopeikin; Yoshiro Sohma; Min Li; Tzyh-Chang Hwang
Journal:  J Gen Physiol       Date:  2010-11-15       Impact factor: 4.086

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