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PMID: 6151683 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Review

Receptors on red cells for Plasmodium falciparum and their interaction with merozoites.

Pasvol G

Abstract

The red cell sialoglycoproteins (glycophorins, alpha (A), delta (B) and beta and gamma (C] play a crucial role in the invasion of human red cells by merozoites of Plasmodium falciparum. Red cells deficient in any of the glycophorins, including beta (also known as glycoconnectin), resist infection by this parasite to varying degrees. These cells and other naturally occurring well-characterized glycophorin variants provide extremely powerful tools to dissect the role of these molecules in invasion. The binding of merozoites to human red cells appears analogous to the binding of wheatgerm agglutinin to sialoglycoconjugates. In both systems O- and N-linked oligosaccharides may be involved. Membrane lipid has not been implicated as a receptor for merozoites, but may instead non-specifically modify binding, as may electrostatic and hydrophobic interactions. The results of data using monoclonal antibodies and lectins, although possibly helpful in identifying specific determinants, must be interpreted with caution. Overall the data suggest that the red cell receptors for all strains of P. falciparum tested to date are located on the glycophorins. Accordingly these putative receptors have been used to affinity-purify complementary parasite components which may yet prove to be of protective immunological significance in a vaccine.

MeSH Terms
Animals Antibodies, Monoclonal Antigens, Protozoan Binding Sites Carbohydrates/blood Erythrocytes/parasitology Glycophorins/physiology Humans Lectins/pharmacology Malaria/blood,immunology,parasitology Plasmodium falciparum/growth & development,immunology
Chemicals
Antibodies, Monoclonal Antigens, Protozoan Carbohydrates Glycophorins Lectins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Pasvol G
Article Info
Journal
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
Abbr.
Philos Trans R Soc Lond B Biol Sci
ISSN
0962-8436
Published
1984-11-13
Pages
189-200
Language
English
Region
England
NLM ID
7503623
Subset
IM
Grants
Wellcome Trust · United Kingdom
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