Abstract
Infrared spectroscopy was used to evaluate the effect of non-iron porphyrins (protoporphyrin IX and haematoporphyrin) on haematin polymerisation to beta-haematin at acidic pH. Both molecules effectively inhibited the reaction, with haematoporphyrin 6 times as active as protoporphyrin IX. We postulated that the interaction between the pi electron system of porphyrin rings leads to the formation of pi-pi adducts, which inhibit polymer elongation in the same way as antimalarial drugs (e.g., chloroquine); the presence of hydroxyl groups able to bind haem iron enhances activity.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antimalarials / metabolism
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Chloroquine / antagonists & inhibitors*
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Chloroquine / metabolism
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Dimerization
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Hematoporphyrins / pharmacology*
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Hemeproteins / antagonists & inhibitors*
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Hemeproteins / metabolism
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Hemin / antagonists & inhibitors*
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Hemin / metabolism
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Humans
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Malaria, Falciparum / metabolism
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Polymers / metabolism*
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Protoporphyrins / pharmacology*
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Spectroscopy, Fourier Transform Infrared
Substances
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Antimalarials
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Hematoporphyrins
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Hemeproteins
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Polymers
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Protoporphyrins
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ferriprotoporphyrin IX-chloroquine complex
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hemozoin
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Hemin
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Chloroquine
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protoporphyrin IX