Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-3038
Biophys J 2004 Dec 01;876:3826-41. doi: 10.1529/biophysj.104.050534.
Show Gene links Show Anatomy links

CFTR: a cysteine at position 338 in TM6 senses a positive electrostatic potential in the pore.

Liu X , Zhang ZR , Fuller MD , Billingsley J , McCarty NA , Dawson DC .


???displayArticle.abstract???
We investigated the accessibility to protons and thiol-directed reagents of a cysteine substituted at position 338 in transmembrane segment 6 (TM6) of CFTR to test the hypothesis that T338 resides in the pore. Xenopus oocytes expressing T338C CFTR exhibited pH-dependent changes in gCl and I-V shape that were specific to the substituted cysteine. The apparent pKa of T338C CFTR was more acidic than that expected for a cysteine or similar simple thiols in aqueous solution. The pKa was shifted toward alkaline values when a nearby positive charge (R334) was substituted with neutral or negatively charged residues, consistent with the predicted influence of the positive charge of R334, and perhaps other residues, on the titration of a cysteine at 338. The relative rates of chemical modification of T338C CFTR by MTSET+ and MTSES- were also altered by the charge at 334. These observations support a model for CFTR that places T338 within the anion conduction path. The apparent pKa of a cysteine substituted at 338 and the relative rates of reaction of charged thiol-directed reagents provide a crude measure of a positive electrostatic potential that may be due to R334 and other residues near this position in the pore.

???displayArticle.pubmedLink??? 15361410
???displayArticle.pmcLink??? PMC1304894
???displayArticle.link??? Biophys J
???displayArticle.grants??? [+]

Species referenced: Xenopus laevis
Genes referenced: cftr

References [+] :
Akabas, Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator. 1998, Pubmed, Xenbase