Literature DB >> 9027746

Hemoglobin catabolism and iron utilization by malaria parasites.

P J Rosenthal1, S R Meshnick.   

Abstract

Erythrocytic malaria parasites transport large quantities of erythrocyte cytoplasm to an acidic food vacuole, where hemoglobin is degraded. Globin is hydrolysed to free amino acids, which are subsequently incorporated into parasite proteins. Potentially toxic heme moieties are polymerized to hemozoin and also probably provide necessary parasite iron. Our understanding of the precise mechanisms of hemoglobin processing is incomplete. However, it is clear that hemoglobin catabolism and related events in the malarial food vacuole are the likely targets of both important antimalarial drugs and of promising new compounds. Thus, a more precise characterization of the metabolism of hemoglobin and iron by malaria parasites should expedite the development of new modes of antimalarial chemotherapy.

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Year:  1996        PMID: 9027746     DOI: 10.1016/s0166-6851(96)02763-6

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  32 in total

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2.  Colorimetric high-throughput screen for detection of heme crystallization inhibitors.

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4.  Antimalarial synergy of cysteine and aspartic protease inhibitors.

Authors:  A Semenov; J E Olson; P J Rosenthal
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5.  Rerooting the evolutionary tree of malaria parasites.

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Review 6.  Monocyte-derived dendritic cells in malaria.

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7.  Gene disruption confirms a critical role for the cysteine protease falcipain-2 in hemoglobin hydrolysis by Plasmodium falciparum.

Authors:  Puran S Sijwali; Philip J Rosenthal
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-15       Impact factor: 11.205

8.  Heme and blood-feeding parasites: friends or foes?

Authors:  Shu Qin Toh; Amber Glanfield; Geoffrey N Gobert; Malcolm K Jones
Journal:  Parasit Vectors       Date:  2010-11-18       Impact factor: 3.876

9.  Separation of Plasmodium falciparum late stage-infected erythrocytes by magnetic means.

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Journal:  J Vis Exp       Date:  2013-03-02       Impact factor: 1.355

10.  Artemisinin triggers a G1 cell cycle arrest of human Ishikawa endometrial cancer cells and inhibits cyclin-dependent kinase-4 promoter activity and expression by disrupting nuclear factor-κB transcriptional signaling.

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