Literature DB >> 11585852

CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction.

S S Smith1, X Liu, Z R Zhang, F Sun, T E Kriewall, N A McCarty, D C Dawson.   

Abstract

The goal of the experiments described here was to explore the possible role of fixed charges in determining the conduction properties of CFTR. We focused on transmembrane segment 6 (TM6) which contains four basic residues (R334, K335, R347, and R352) that would be predicted, on the basis of their positions in the primary structure, to span TM6 from near the extracellular (R334, K335) to near the intracellular (R347, R352) end. Cysteines substituted at positions 334 and 335 were readily accessible to thiol reagents, whereas those at positions 347 and 352 were either not accessible or lacked significant functional consequences when modified. The charge at positions 334 and 335 was an important determinant of CFTR channel function. Charge changes at position 334--brought about by covalent modification of engineered cysteine residues, pH titration of cysteine and histidine residues, and amino acid substitution--produced similar effects on macroscopic conductance and the shape of the I-V plot. The effect of charge changes at position 334 on conduction properties could be described by electrodiffusion or rate-theory models in which the charge on this residue lies in an external vestibule of the pore where it functions to increase the concentration of Cl adjacent to the rate-limiting portion of the conduction path. Covalent modification of R334C CFTR increased single-channel conductance determined in detached patches, but did not alter open probability. The results are consistent with the hypothesis that in wild-type CFTR, R334 occupies a position where its charge can influence the distribution of anions near the mouth of the pore.

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Year:  2001        PMID: 11585852      PMCID: PMC2233702          DOI: 10.1085/jgp.118.4.407

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  51 in total

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2.  On the use of thiol-modifying agents to determine channel topology.

Authors:  M Holmgren; Y Liu; Y Xu; G Yellen
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3.  Chloride conductance expressed by delta F508 and other mutant CFTRs in Xenopus oocytes.

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4.  cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor.

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5.  Identification and molecular localization of a pH-sensing domain for the inward rectifier potassium channel HIR.

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Review 6.  CFTR: mechanism of anion conduction.

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9.  On the mechanism of rectification of the isoproterenol-activated chloride current in guinea-pig ventricular myocytes.

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4.  Thermal instability of ΔF508 cystic fibrosis transmembrane conductance regulator (CFTR) channel function: protection by single suppressor mutations and inhibiting channel activity.

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5.  Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.

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6.  Small molecule correctors of F508del-CFTR discovered by structure-based virtual screening.

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7.  Cystic fibrosis transmembrane conductance regulator: temperature-dependent cysteine reactivity suggests different stable conformers of the conduction pathway.

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Review 9.  Architecture and functional properties of the CFTR channel pore.

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10.  Cystic fibrosis transmembrane conductance regulator: using differential reactivity toward channel-permeant and channel-impermeant thiol-reactive probes to test a molecular model for the pore.

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