Source:http://linkedlifedata.com/resource/pubmed/id/17290993
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2007-3-1
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pubmed:abstractText |
The morphology of micrometer-sized beta-hematin crystals (synthetic malaria pigment) was determined by TEM images and diffraction, and by grazing incidence synchrotron X-ray diffraction at the air-water interface. The needle-like crystals are bounded by sharp {100} and {010} side faces, and capped by {011} and, to a lesser extent, by {001} end faces, in agreement with hemozoin (malaria pigment) crystals. The beta-hematin crystals grown in the presence of 10% chloroquine or quinine took appreciably longer to precipitate and tended to be symmetrically tapered toward both ends of the needle, due to stereoselective additive binding to {001} or {011} ledges. Evidence, but marginal, is presented that additives reduce crystal mosaic domain size along the needle axis, based on X-ray powder diffraction data. Coherent grazing exit X-ray diffraction suggests that the mosaic domains are smaller and less structurally stable than in pure crystals. IR-ATR and Raman spectra indicate molecular based differences due to a modification of surface and bulk propionic acid groups, following additive binding and a molecular rearrangement in the environment of the bulk sites poisoned by occluded quinoline. These results provided incentive to examine computationally whether hemozoin may be a target of antimalarial drugs diethylamino-alkoxyxanthones and artemisinin. A variation in activity of the former as a function of the alkoxy chain length is correlated with computed binding energy to {001} and {011} faces of beta-hematin. A model is proposed for artemisinin activity involving hemozoin nucleation inhibition via artemisinin-beta-hematin adducts bound to the principal crystal faces. Regarding nucleation of hemozoin inside the digestive vacuole of the malaria parasite, nucleation via the vacuole's membranous surface is proposed, based on a reported hemozoin alignment. As a test, a dibehenoyl-phosphatidylcholine monolayer transferred onto OTS-Si wafer nucleated far more beta-hematin crystals, albeit randomly oriented, than a reference OTS-Si.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antimalarials,
http://linkedlifedata.com/resource/pubmed/chemical/Chloroquine,
http://linkedlifedata.com/resource/pubmed/chemical/Hemeproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Propionic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Quinolines,
http://linkedlifedata.com/resource/pubmed/chemical/hemozoin,
http://linkedlifedata.com/resource/pubmed/chemical/propionic acid,
http://linkedlifedata.com/resource/pubmed/chemical/quinoline
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0002-7863
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pubmed:author |
pubmed-author:BaehtzCarstenC,
pubmed-author:FeldmanYishayY,
pubmed-author:KjaerKristianK,
pubmed-author:LeiserowitzLeslieL,
pubmed-author:McNaughtonDonD,
pubmed-author:OsipovaMariaM,
pubmed-author:RobinsonIan KIK,
pubmed-author:SolomonovInnaI,
pubmed-author:WebsterGrant TGT,
pubmed-author:WeissbuchIsabelleI,
pubmed-author:WoodBayden RBR
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pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:volume |
129
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2615-27
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17290993-Animals,
pubmed-meshheading:17290993-Antimalarials,
pubmed-meshheading:17290993-Binding Sites,
pubmed-meshheading:17290993-Chemical Precipitation,
pubmed-meshheading:17290993-Chloroquine,
pubmed-meshheading:17290993-Dimerization,
pubmed-meshheading:17290993-Drug Delivery Systems,
pubmed-meshheading:17290993-Hemeproteins,
pubmed-meshheading:17290993-Microscopy, Electron, Transmission,
pubmed-meshheading:17290993-Propionic Acids,
pubmed-meshheading:17290993-Quinolines,
pubmed-meshheading:17290993-Spectrum Analysis, Raman,
pubmed-meshheading:17290993-Stereoisomerism,
pubmed-meshheading:17290993-X-Ray Diffraction
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pubmed:year |
2007
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pubmed:articleTitle |
Crystal nucleation, growth, and morphology of the synthetic malaria pigment beta-hematin and the effect thereon by quinoline additives: the malaria pigment as a target of various antimalarial drugs.
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pubmed:affiliation |
Department of Materials and Interfaces, The Weizmann Institute of Science, 76100-Rehovot, Israel.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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