Literature DB >> 2155022

Reconstitution of a kidney chloride channel and its identification by covalent labeling.

W Breuer1.   

Abstract

The basolateral membrane of the thick ascending loop of Henle (TALH) of the mammalian kidney is characterized by its high content of Na+/K(+)-ATPase and a Cl- conductance, which function in parallel in salt reabsorption. In order to reconstitute the Cl- channels, TALH membrane vesicles were solubilized in 1% sodium cholate in buffer containing 200 mM KCl, followed by dilution with soybean lipids (final ratio of protein/detergent/lipid of 1:3:15 in mg) and removal of the detergent by gel filtration on Sephadex G-50. Cl- channel activity in the liposomes was determined by a 36Cl- uptake assay where the accumulation of the radioactive tracer against its chemical gradient is driven by the membrane potential (positive inside) generated by an outward Cl- gradient. The 36Cl- uptake by the KCl-loaded liposomes was dependent on the inclusion of membrane protein and was abolished by valinomycin, indicating the involvement of a conductive pathway. It was also inhibited by 36% by 100 microM 4,4'-diisothiocyanostilbene-2,2'-disulfonate (DIDS) and 5-nitro-2-(3-phenylpropylamino)benzoic acid (NPPB). Solubilization of the Cl- channels in cholate was optimal in the presence of 200 mm KCl, but was found to decrease markedly at low ionic strength. SDS-PAGE analysis of the proteins extracted by cholate at high and low salt concentrations showed that the Cl- channel-containing high KCl extract was enriched in the 96 and 55 kDa alpha- and beta-subunits of the Na+/K(+)-ATPase (the major proteins in the membrane preparation) and several minor protein bands. Treatment of the membrane vesicles with the radioactive analogue of DIDS, [3H]2DIDS, labeled primarily a 65 and a 31 kDa protein. The solubilization of the 31 kDa protein by cholate depended markedly on the ionic strength and thus paralleled the solubilization pattern of Cl- channel activity. Furthermore, the labeling of the 31 kDa protein was prevented by nonradioactive DIDS and by NPPB but not by other compounds, indicating that it may be a Cl- channel component.

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Year:  1990        PMID: 2155022     DOI: 10.1016/0005-2736(90)90118-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

1.  Methodology for assaying iodide conductance in proteoliposomes: specific induction by thyroid membrane protein.

Authors:  P E Golstein; A Sener; R Beauwens
Journal:  Biochem J       Date:  1995-12-01       Impact factor: 3.857

Review 2.  Molecular basis of epithelial Cl channels.

Authors:  P Fong; T J Jentsch
Journal:  J Membr Biol       Date:  1995-04       Impact factor: 1.843

Review 3.  [A flip-flop model of the chloride channel complex explains the dysregulation of the chloride flow in the plasmalemma of cells in cystic fibrosis].

Authors:  F P Thinnes; D Babel; A Hein; L Jürgens; U König; A Schmid; N Hilschmann
Journal:  Klin Wochenschr       Date:  1991-05-03

4.  Halide permeation through three types of epithelial anion channels after reconstitution into giant liposomes.

Authors:  M Duszyk; D Liu; A S French; S F Man
Journal:  Eur Biophys J       Date:  1993       Impact factor: 1.733

5.  Factors affecting chloride conductance in apical membrane vesicles from human placenta.

Authors:  D Faller; M P Ryan
Journal:  J Membr Biol       Date:  1992-12       Impact factor: 1.843

  5 in total

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