Non-iron porphyrins inhibit beta-haematin (malaria pigment) polymerisation

FEBS Lett. 1997 Jun 9;409(2):297-9. doi: 10.1016/s0014-5793(97)00533-4.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials / metabolism
  • Chloroquine / antagonists & inhibitors*
  • Chloroquine / metabolism
  • Dimerization
  • Hematoporphyrins / pharmacology*
  • Hemeproteins / antagonists & inhibitors*
  • Hemeproteins / metabolism
  • Hemin / antagonists & inhibitors*
  • Hemin / metabolism
  • Humans
  • Malaria, Falciparum / metabolism
  • Polymers / metabolism*
  • Protoporphyrins / pharmacology*
  • Spectroscopy, Fourier Transform Infrared

Substances

  • Antimalarials
  • Hematoporphyrins
  • Hemeproteins
  • Polymers
  • Protoporphyrins
  • ferriprotoporphyrin IX-chloroquine complex
  • hemozoin
  • Hemin
  • Chloroquine
  • protoporphyrin IX