The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Reaction of antimalarial endoperoxides with specific parasite proteins
Open accessAbstract
The endoperoxides are a new class of antimalarial agents, of which artemisinin (qinghaosu) is the prototype. We have previously shown that artemisinin is capable of alkylating proteins in model reactions. In the present study, we showed that when Plasmodium falciparum-infected erythrocytes are treated with a radiolabeled antimalarial endoperoxide, either arteether, dihydroartemisinin, or Ro 42-1611 (arteflene), the radioactivity is largely coverted into a form which can be extracted with sodium dodecyl sulfate (SDS). Autoradiograms of SDS-polyacrylamide gels showed that six malarial proteins are radioactively labeled by the three endoperoxides. This labeling occurs at physiological concentrations of drug and is not stage nor strain specific. The labeled proteins were not the most abundant proteins seen on Coomassie-stained gels. No proteins were labeled when uninfected erythrocytes were treated with these drugs, nor when infected erythrocytes were treated with the inactive analog deoxyarteether. Thus, the antimalarial endoperoxides appear to react with specific malarial proteins.
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Citations
Cites
Iron-dependent free radical generation from the antimalarial agent artemisinin (qinghaosu)
Meshnick, S. R., Yang, Y. Z., Lima, V, Kuypers, F., Kamchonwongpaisan, S., & Yuthavong, Y. (1993) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.37.5.1108 · Cited by 327
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Cited by
A Medicinal Chemistry Perspective on Artemisinin and Related Endoperoxides
O'Neill, P. M., & Posner, G. H. (2004) · Journal of Medicinal Chemistry · doi:10.1021/jm030571c · Cited by 538
Discovery, mechanisms of action and combination therapy of artemisinin
Cui, L., & Su, X.-Z. (2009) · Expert Review of Anti-infective Therapy · doi:10.1586/eri.09.68 · Cited by 371
Artemisinin and the antimalarial endoperoxides: from herbal remedy to targeted chemotherapy
Meshnick, S. R., Taylor, T. E., & Kamchonwongpaisan, S. (1996) · Microbiological Reviews · doi:10.1128/mmbr.60.2.301-315.1996 · Cited by 710
“Importantly, the labeled proteins seem to be concentrated in a crude parasite membrane fraction (7), which is consistent with the affinity of the drug for membranes discussed above.”
BackgroundInfluentialSelf-citationBerdelle, N., Nikolova, T., Quiros, S., Efferth, T., & Kaina, B. (2011) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-11-0534 · Cited by 181
The mode of action of the antimalarial artemisinin and its derivatives
Kamchonwongpaisan, S., & Meshnick, S. R. (1996) · General Pharmacology: The Vascular System · doi:10.1016/0306-3623(95)02047-0 · Cited by 77
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Metadata
- Authors
- Asawamahasakda, W., Ittarat, I., Pu, Y. M., Ziffer, H., & Meshnick, S. R.
- Venue
- Antimicrobial Agents and Chemotherapy
- Publisher
- American Society for Microbiology
- Published
- 1994-08
- Volume
- 38
- Issue
- 8
- Pages
- 1854-1858
- ISSN
- 0066-4804 (ISSN-L)
- 1098-6596
- OpenAlex
- W2022012565
- Cited by
- 234
- References
- 1
- FWCI
- 11.83
- Type
- journal article
- Language
- en
- Open access
- green
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- Asawamahasakda, W., Ittarat, I., Pu, Y. M., Ziffer, H., & Meshnick, S. R. (1994). Reaction of antimalarial endoperoxides with specific parasite proteins. Antimicrobial Agents and Chemotherapy. https://doi.org/10.1128/aac.38.8.1854
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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