Erythrocyte detergent-resistant membrane proteins: their characterization and selective uptake during malarial infection.

Infection of human erythrocytes by the apicomplexan malaria parasite Plasmodium falciparum results in endovacuolar uptake of 4 host proteins that reside in erythrocyte detergent-resistant membranes (DRMs). Whether this vacuolar transport reflects selective uptake of host DRM proteins remains unknown. A further complication is that DRMs of vastly different protein and cholesterol contents have been isolated from erythrocytes. Here we show that isolated DRMs containing the highest cholesterol-to-protein ratio have low protein mass. Liquid chromatography, mass spectrometry, and antibody-based studies reveal that the major DRM proteins are band 3, flotillin-1 and -2, peroxiredoxin-2, and stomatin. Band 3 and stomatin, which reflect the bulk mass of erythrocyte DRM proteins, and all tested non-DRM proteins are excluded from the vacuolar parasite. In contrast, flotillin-1 and -2 and 8 minor DRM proteins are recruited to the vacuole. These data suggest that DRM association is necessary but not sufficient for vacuolar recruitment and there is active, vacuolar uptake of a subset of host DRM proteins. Finally, the 10 internalized DRM proteins show varied lipid and peptidic anchors indicating that, contrary to the prevailing model of apicomplexan vacuole formation, DRM association, rather than lipid anchors, provides the preferred criteria for protein recruitment to the malarial vacuole.

[1]  K. Joiner Faculty Opinions recommendation of Identification of a stomatin orthologue in vacuoles induced in human erythrocytes by malaria parasites. A role for microbial raft proteins in apicomplexan vacuole biogenesis. , 2003 .

[2]  Travis Harrison,et al.  Erythrocyte G Protein-Coupled Receptor Signaling in Malarial Infection , 2003, Science.

[3]  M. Tanner,et al.  A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane. , 2003, Blood.

[4]  G. Minetti,et al.  New and old integral proteins of the human erythrocyte membrane. , 2003, Blood.

[5]  J. Leszyk,et al.  Proteomic Analysis of a Detergent-resistant Membrane Skeleton from Neutrophil Plasma Membranes* 210 , 2002, The Journal of Biological Chemistry.

[6]  K. Seydel,et al.  Detergent-resistant erythrocyte membrane rafts are modified by a Plasmodium falciparum infection. , 2002, Experimental parasitology.

[7]  K. Haldar,et al.  Protein and lipid trafficking induced in erythrocytes infected by malaria parasites , 2002, Cellular microbiology.

[8]  P. Hinterdorfer,et al.  Ca(++)-dependent vesicle release from erythrocytes involves stomatin-specific lipid rafts, synexin (annexin VII), and sorcin. , 2002, Blood.

[9]  K. Haldar,et al.  The Role of Cholesterol and Glycosylphosphatidylinositol-anchored Proteins of Erythrocyte Rafts in Regulating Raft Protein Content and Malarial Infection* , 2001, The Journal of Biological Chemistry.

[10]  R. Donato,et al.  S100: a multigenic family of calcium-modulated proteins of the EF-hand type with intracellular and extracellular functional roles. , 2001, The international journal of biochemistry & cell biology.

[11]  R. Rebres,et al.  Membrane Raft Association of CD47 Is Necessary for Actin Polymerization and Protein Kinase C θ Translocation in Its Synergistic Activation of T Cells* , 2001, The Journal of Biological Chemistry.

[12]  R. Prohaska,et al.  Stomatin, flotillin-1, and flotillin-2 are major integral proteins of erythrocyte lipid rafts. , 2001, Blood.

[13]  K. Haldar,et al.  Vacuolar uptake of host components, and a role for cholesterol and sphingomyelin in malarial infection , 2000, The EMBO journal.

[14]  A. Carruthers,et al.  ATP-dependent substrate occlusion by the human erythrocyte sugar transporter. , 2000, Biochemistry.

[15]  J. Poole Red cell antigens on band 3 and glycophorin A. , 2000, Blood reviews.

[16]  S. Hamill,et al.  The human erythrocyte sugar transporter presents two sugar import sites. , 1999, Biochemistry.

[17]  L. Sibley,et al.  Invasion by Toxoplasma gondii Establishes a Moving Junction That Selectively Excludes Host Cell Plasma Membrane Proteins on the Basis of Their Membrane Anchoring , 1999, The Journal of experimental medicine.

[18]  D. Vestweber,et al.  Molecular mechanisms that control leukocyte extravasation: the selectins and the chemokines. , 1999, Histochemistry and cell biology.

[19]  D. Golan,et al.  Regulation of band 3 rotational mobility by ankyrin in intact human red cells. , 1998, Biochemistry.

[20]  D. Hoessli,et al.  Effects of cholesterol depletion by cyclodextrin on the sphingolipid microdomains of the plasma membrane. , 1998, The Biochemical journal.

[21]  William Arbuthnot Sir Lane,et al.  Rabbit beta-globin is extended beyond its UGA stop codon by multiple suppressions and translational reading gaps. , 1998, Biochemistry.

[22]  P. Bütikofer,et al.  In vitro incorporation of GPI-anchored proteins into human erythrocytes and their fate in the membrane. , 1998, Blood.

[23]  D. Brown,et al.  Structure of detergent-resistant membrane domains: does phase separation occur in biological membranes? , 1997, Biochemical and biophysical research communications.

[24]  P. Verkade,et al.  Lipid microdomains and membrane trafficking in mammalian cells , 1997, Histochemistry and Cell Biology.

[25]  E. Ikonen,et al.  Functional rafts in cell membranes , 1997, Nature.

[26]  P. V. van Zijl,et al.  Functional Analysis of Aquaporin-1 Deficient Red Cells , 1996, The Journal of Biological Chemistry.

[27]  J. Yates,et al.  An approach to correlate tandem mass spectral data of peptides with amino acid sequences in a protein database , 1994, Journal of the American Society for Mass Spectrometry.

[28]  D. Golan,et al.  Differential control of band 3 lateral and rotational mobility in intact red cells. , 1994, The Journal of clinical investigation.

[29]  K. Kim,et al.  Purification and characterization of thiol-specific antioxidant protein from human red blood cell: a new type of antioxidant protein. , 1994, Biochemical and biophysical research communications.

[30]  P. Schuck,et al.  Band 3‐hemoglobin associations The band 3 tetramer is the oxyhemoglobin binding site , 1991, FEBS letters.

[31]  R. Moore,et al.  Reconstitution of Ca(2+)-dependent K+ transport in erythrocyte membrane vesicles requires a cytoplasmic protein. , 1991, The Journal of biological chemistry.

[32]  P. Agre,et al.  Erythrocyte Mr 28,000 transmembrane protein exists as a multisubunit oligomer similar to channel proteins. , 1991, The Journal of biological chemistry.

[33]  P. Low,et al.  Structural stability of the erythrocyte anion transporter, band 3, in different lipid environments. A differential scanning calorimetric study. , 1988, The Journal of biological chemistry.

[34]  W. Trager,et al.  Human malaria parasites in continuous culture. , 1976, Science.

[35]  D. Brown,et al.  Functions of lipid rafts in biological membranes. , 1998, Annual review of cell and developmental biology.

[36]  K. Haldar,et al.  In vitro secretory assays with erythrocyte-free malaria parasites. , 1994, Methods in cell biology.