Literature DB >> 7599149

Reconstitution of lysosomal sulfate transport in proteoliposomes.

P J Koetters1, H F Chou, A J Jonas.   

Abstract

As part of a strategy to purify the lysosomal sulfate transporter, we developed a method for reconstitution of transport in artificial membrane vesicles. Lysosomal membranes were prepared from Percoll density gradient purified rat liver lysosomes and membrane proteins were solubilized using the non-ionic detergent, Triton X-100. The solubilized proteins were mixed with liposomes prepared by sonication of egg yolk lecithin and the detergent was removed by passage of the mixture over Bio-beads XAD2. The resulting proteoliposomes exhibited saturable sulfate transport with characteristics that were very similar to those observed in lysosomal membranes. Transport in proteoliposomes had a Km of 155 microM, exhibited pH dependence and was sensitive to inhibition by DIDS. Reconstitution of transport in proteoliposomes may be useful as an assay for purification of the lysosomal sulfate carrier.

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Year:  1995        PMID: 7599149     DOI: 10.1016/0304-4165(95)00036-b

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


  1 in total

1.  Lysosomal sulphate transport is dependent upon sulphydryl groups.

Authors:  H F Chou; M Passage; A J Jonas
Journal:  Biochem J       Date:  1998-03-01       Impact factor: 3.857

  1 in total

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