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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1985-5-30
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pubmed:abstractText |
The host cell membrane of Plasmodium falciparum infected cells becomes permeabilized at the trophozoite stage. A variety of otherwise impermeant substances such as carbohydrates, polyols, amino acids and anions easily gain access to the cytosol of infected cells. Using the isotonic-hemolysis method or uptake of labeled substances, we characterized the new permeation pathways as pores of approximately 0.7 nm equivalent radius. The pores bear a positively charged character which facilitates movement of small anions and excludes cations, so that the ionic composition and osmotic properties of infected cells are not drastically altered. Substances of a molecular size similar to that of disaccharides are fully excluded. Substances of limiting size might be accommodated in the pore, provided they bear a side group of hydrophobic character. The new permeation pathways may provide a vital route for acquisition or release of essential nutrients or catabolites.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0166-6851
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
313-22
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3887158-Amino Acids,
pubmed-meshheading:3887158-Animals,
pubmed-meshheading:3887158-Biological Transport, Active,
pubmed-meshheading:3887158-Carbohydrates,
pubmed-meshheading:3887158-Cell Membrane Permeability,
pubmed-meshheading:3887158-Erythrocytes,
pubmed-meshheading:3887158-Hemolysis,
pubmed-meshheading:3887158-Humans,
pubmed-meshheading:3887158-Malaria,
pubmed-meshheading:3887158-Plasmodium falciparum
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pubmed:year |
1985
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pubmed:articleTitle |
Characterization of permeation pathways appearing in the host membrane of Plasmodium falciparum infected red blood cells.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|