Literature DB >> 6490754

Partial purification of a membrane glycoprotein antigen by high-pressure size-exclusion chromatography without loss of antigenicity.

P Lambotte, J Van Snick, T Boon.   

Abstract

A high-pressure size exclusion chromatography system eluted with phosphate saline buffer containing 0.25% sodium deoxycholate has been developed that fractionates both soluble and membrane glycoproteins with good resolution and molecular weight versus elution time relationship. Using this system we fractionated membrane glycoproteins from a mutagenized mastocytoma cell that carries a strong transplantation antigen. After dialysis to remove the detergent, the fractions were tested for biological activity by an in vitro assay involving T-lymphocyte cell culture. Antigenic activity was found between 43 and 85 kdaltons. This demonstrates the efficiency of the system to resolve complex membrane protein samples without destroying their biological activity.

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Year:  1984        PMID: 6490754     DOI: 10.1016/s0021-9673(01)89037-3

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  Immunogenic (tum-) variants obtained by mutagenesis of mouse mastocytoma P815. VIII. Detection of stable transfectants expressing a tum- antigen with a cytolytic T cell stimulation assay.

Authors:  T Wölfel; A Van Pel; E De Plaen; C Lurquin; J L Maryanski; T Boon
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

Review 2.  Column liquid chromatography of integral membrane proteins.

Authors:  G W Welling; R van der Zee; S Welling-Wester
Journal:  J Chromatogr       Date:  1987-07-17
  2 in total

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