Trafficked Proteins—Druggable inPlasmodium falciparum?
Author(s) -
Jasmin Lindner,
Kamila Anna Meissner,
Isolmar Tadeu Schettert,
Carsten Wrenger
Publication year - 2013
Publication title -
international journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.587
H-Index - 53
eISSN - 1687-8884
pISSN - 1687-8876
DOI - 10.1155/2013/435981
Subject(s) - druggability , malaria , apicoplast , plasmodium falciparum , disease , medicine , drug resistance , drug , biology , bioinformatics , virology , immunology , pharmacology , apicomplexa , genetics , gene , pathology
Malaria is an infectious disease that results in serious health problems in the countries in which it is endemic. Annually this parasitic disease leads to more than half a million deaths; most of these are children in Africa. An effective vaccine is not available, and the treatment of the disease is solely dependent on chemotherapy. However, drug resistance is spreading, and the identification of new drug targets as well as the development of new antimalarials is urgently required. Attention has been drawn to a variety of essential plasmodial proteins, which are targeted to intra- or extracellular destinations, such as the digestive vacuole, the apicoplast, or into the host cell. Interfering with the action or the transport of these proteins will impede proliferation of the parasite. In this mini review, we will shed light on the present discovery of chemotherapeutics and potential drug targets involved in protein trafficking processes in the malaria parasite.
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