Literature DB >> 6379454

Identification of parasite proteins in a membrane preparation enriched for the surface membrane of erythrocytes infected with Plasmodium knowlesi.

S B Aley, J W Barnwell, W Daniel, R J Howard.   

Abstract

A subcellular fraction enriched in erythrocyte membranes has been isolated from rhesus monkey erythrocytes infected with Plasmodium knowlesi. Infected cells were lysed by centrifugation through a zone of hypotonic buffer and membranes isolated by equilibrium density gradient centrifugation in the same tube. The purified membrane fraction was shown to include the erythrocyte surface membrane by several methods: electron microscopy, identification of Coomassie Blue stained erythrocyte membrane proteins, identification of band 3 with a monoclonal antibody, and identification of radioiodinated cell surface proteins. The resulting ghosts were shown to be specifically reactive with monkey sera against the variant surface antigens of P. knowlesi by indirect immunofluorescence and membrane agglutination. No reactivity was seen with a monoclonal antibody (13C11) against the intracellular schizont surface. A number of metabolically labelled parasite proteins were enriched in this membrane function, including peptides of 277, 208, 173, 153, 134, 109, 80, 60 and 48 kDa and the variant surface antigens of variable molecular mass (180-207 kDa). These proteins were distinct from the major parasite proteins of total infected erythrocytes and isolated merozoites. The major glucosamine labelled glycoprotein of the internal schizont (230 kDa) was not found in this fraction. Moreover, no fragment of this parasite glycoprotein was found in this membrane fraction, indicating that no part of this molecule is transported to the erythrocyte surface. In contrast, the variant antigen of P. knowlesi, known to be on the erythrocyte surface, could be readily identified as peptides unique to specific cloned parasite lines. We propose that the other nine parasite proteins found within this membrane fraction represent a starting point for the identification of other parasite proteins transported to the surface membrane of the infected erythrocyte.

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Year:  1984        PMID: 6379454     DOI: 10.1016/0166-6851(84)90045-8

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  8 in total

1.  Rapid transport of the acidic phosphoproteins of Plasmodium berghei and P. chabaudi from the intraerythrocytic parasite to the host membrane using a miniaturized fractionation procedure.

Authors:  M F Wiser; H N Lanners
Journal:  Parasitol Res       Date:  1992       Impact factor: 2.289

2.  The ring-infected erythrocyte surface antigen (RESA) of Plasmodium falciparum stabilizes spectrin tetramers and suppresses further invasion.

Authors:  Xinhong Pei; Xinhua Guo; Ross Coppel; Souvik Bhattacharjee; Kasturi Haldar; Walter Gratzer; Narla Mohandas; Xiuli An
Journal:  Blood       Date:  2007-04-27       Impact factor: 22.113

3.  Improved isolation of Plasmodium knowlesi-infected erythrocyte host-cell membrane on polycationic beads.

Authors:  H J Vial; P H Van der Schaft; B D Beaumelle; M J Thuet; J A Op den Kamp
Journal:  Parasitol Res       Date:  1989       Impact factor: 2.289

4.  Plasmodium falciparum-infected erythrocytes do not adhere well to C32 melanoma cells or CD36 unless rosettes with uninfected erythrocytes are first disrupted.

Authors:  S M Handunnetti; T H Hasler; R J Howard
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

5.  Spleen-dependent regulation of antigenic variation in malaria parasites: Plasmodium knowlesi SICAvar expression profiles in splenic and asplenic hosts.

Authors:  Stacey A Lapp; Cindy Korir-Morrison; Jianlin Jiang; Yaohui Bai; Vladimir Corredor; Mary R Galinski
Journal:  PLoS One       Date:  2013-10-18       Impact factor: 3.240

6.  Secretion of a soluble class I molecule encoded by the Q10 gene of the C57BL/10 mouse.

Authors:  J J Devlin; A M Lew; R A Flavell; J E Coligan
Journal:  EMBO J       Date:  1985-02       Impact factor: 11.598

7.  Redefining the expressed prototype SICAvar gene involved in Plasmodium knowlesi antigenic variation.

Authors:  Stacey A Lapp; Cindy C Korir; Mary R Galinski
Journal:  Malar J       Date:  2009-07-31       Impact factor: 2.979

8.  Knob-positive and knob-negative Plasmodium falciparum differ in expression of a strain-specific malarial antigen on the surface of infected erythrocytes.

Authors:  S B Aley; J A Sherwood; R J Howard
Journal:  J Exp Med       Date:  1984-11-01       Impact factor: 14.307

  8 in total

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