Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Mol Cell ; 6(4): 861-71, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11090624

ABSTRACT

The determinant of verapamil-reversible chloroquine resistance (CQR) in a Plasmodium falciparum genetic cross maps to a 36 kb segment of chromosome 7. This segment harbors a 13-exon gene, pfcrt, having point mutations that associate completely with CQR in parasite lines from Asia, Africa, and South America. These data, transfection results, and selection of a CQR line harboring a novel K761 mutation point to a central role for the PfCRT protein in CQR. This transmembrane protein localizes to the parasite digestive vacuole (DV), the site of CQ action, where increased compartment acidification associates with PfCRT point mutations. Mutations in PfCRT may result in altered chloroquine flux or reduced drug binding to hematin through an effect on DV pH.


Subject(s)
Chloroquine/pharmacology , Membrane Proteins/metabolism , Plasmodium falciparum/genetics , Protozoan Proteins/genetics , Vacuoles/physiology , Amino Acid Sequence , Animals , Animals, Genetically Modified , Digestive System/metabolism , Drug Resistance , Exons , Humans , Membrane Proteins/chemistry , Membrane Proteins/genetics , Membrane Transport Proteins , Molecular Sequence Data , Mutagenesis, Site-Directed , Plasmodium falciparum/drug effects , Polymerase Chain Reaction , Protozoan Proteins/chemistry , Protozoan Proteins/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Tetrahydrofolate Dehydrogenase/genetics , Transfection , Verapamil/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL
...