Literature DB >> 7686365

Isolation and characterization of renal cortical membranes using an aqueous two-phase partition technique.

T G Hammond1, R R Majewski, J J Onorato, P C Brazy, D J Morré.   

Abstract

The aqueous two-phase partition technique is a simple, rapid and inexpensive method for the fractionation of membrane preparations. Aqueous two-phase partitioning separates according to surface properties such as charge and hydrophobicity, making it complementary to established centrifugation techniques, which separate on the basis of density. Although aqueous two-phase partitioning has been successfully applied to animal tissues, there are limited data on the functional properties of the isolated membranes. We have applied the aqueous two-phase partition technique to rat renal brush-border membrane vesicles and sheets. Our aim was to remove organelle contamination while maintaining the functional properties of the membranes. Evidence from marker enzyme analysis and electron microscopy supports the conclusion that renal brush-border membranes are fractionated separate from the mitochondria and endoplasmic reticulum. This separation procedure did not alter the Na(+)-dependent transport of brush-border membrane vesicles. Na(+)-D-glucose symporter and Na(+)-H+ antiporter activity in the fractionated preparation increased to the same extent as did the enrichment of enzyme markers for brush-border membranes.

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Year:  1993        PMID: 7686365      PMCID: PMC1134176          DOI: 10.1042/bj2920743

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  20 in total

1.  Inhibition by bilirubin of (Na+ + K+)-activated adenosine triphosphatase and K+-activated p-nitrophenylphosphatase activities of NaI-treated microsomes from young rat cerebrum.

Authors:  S Kashiwamata; S Goto; R K Semba; F N Suzuki
Journal:  J Biol Chem       Date:  1979-06-10       Impact factor: 5.157

2.  Studies on plasma membranes. II. K+-dependent p-nitrophenyl phosphatase activity of plasma membranes isolated from rat liver.

Authors:  P Emmelot; C J Bos
Journal:  Biochim Biophys Acta       Date:  1966-06-29

3.  The absolute asymmetry of orientation of gamma-glutamyltranspeptidase and aminopeptidase on the external surface of the rat renal brush border membrane.

Authors:  B Tsao; N P Curthoys
Journal:  J Biol Chem       Date:  1980-08-25       Impact factor: 5.157

Review 4.  Phase partition--a method for purification and analysis of cell organelles and membrane vesicles.

Authors:  P A Albertsson; B Andersson; C Larsson; H E Akerlund
Journal:  Methods Biochem Anal       Date:  1982

5.  Na+/H+ antiporter in membrane populations resolved from a renal brush border vesicle preparation.

Authors:  A K Mircheff; H E Ives; V J Yee; D G Warnock
Journal:  Am J Physiol       Date:  1984-06

6.  Study of rat renal brush border membrane vesicles by flow cytometry.

Authors:  T G Hammond
Journal:  Kidney Int       Date:  1990-07       Impact factor: 10.612

7.  Isolation of the sodium-dependent d-glucose transport protein from brush-border membranes.

Authors:  P Malathi; H Preiser
Journal:  Biochim Biophys Acta       Date:  1983-11-23

8.  Assay of succinate dehydrogenase activity by the tetrazolium method: evaluation of an improved technique in skeletal muscle fractions.

Authors:  J D Green; H T Narahara
Journal:  J Histochem Cytochem       Date:  1980-05       Impact factor: 2.479

9.  Stoichiometric studies of the renal outer cortical brush border membrane D-glucose transporter.

Authors:  R J Turner; A Moran
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

10.  Further studies of proximal tubular brush border membrane D-glucose transport heterogeneity.

Authors:  R J Turner; A Moran
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

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  1 in total

1.  Diadenosine polyphosphate-stimulated gluconeogenesis in isolated rat proximal tubules.

Authors:  M Edgecombe; H S Craddock; D C Smith; A G McLennan; M J Fisher
Journal:  Biochem J       Date:  1997-04-15       Impact factor: 3.857

  1 in total

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