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Open AccessJournal ArticleDOI

Exported Proteins Required for Virulence and Rigidity of Plasmodium falciparum-Infected Human Erythrocytes

TLDR
It is shown that multiple proteins play a role in generating increased rigidity of infected erythrocytes and may provide targets for antivirulence based therapies to a disease responsible for millions of deaths annually.
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This article is published in Cell.The article was published on 2008-07-11 and is currently open access. It has received 483 citations till now. The article focuses on the topics: KAHRP & Plasmodium falciparum.

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Cell-Cell Communication between Malaria-Infected Red Blood Cells via Exosome-like Vesicles

TL;DR: This study reveals a previously unidentified pathway of P. falciparum biology critical for survival in the host and transmission to mosquitoes and identifies a pathway for the development of agents to block parasite transmission from the human host to the mosquito.

A Genome-wide CRISPR Screen in Toxoplasma Identifies Essential Apicomplexan Genes

TL;DR: The first genome-wide genetic screen of an apicomplexan parasite is presented, revealing essential functions during infection of human cells and providing broad-based functional information on T. gondii genes that will facilitate future approaches to expand the horizon of antiparasitic interventions.
Journal ArticleDOI

Functional Profiling of a Plasmodium Genome Reveals an Abundance of Essential Genes

TL;DR: The genomes of malaria parasites contain many genes of unknown function and the level of genetic redundancy in a single-celled organism may reflect the degree of environmental variation it experiences, which helps rationalize both the relative successes of drugs and the greater difficulty of making an effective vaccine.
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A newly discovered protein export machine in malaria parasites

TL;DR: This work has identified in Plasmodium falciparum a translocon of exported proteins (PTEX), which is located in the vacuole membrane and offers a new avenue for therapeutic intervention.
References
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Journal ArticleDOI

Functional profiling of the Saccharomyces cerevisiae genome.

Guri Giaever, +72 more
- 25 Jul 2002 - 
TL;DR: It is shown that previously known and new genes are necessary for optimal growth under six well-studied conditions: high salt, sorbitol, galactose, pH 8, minimal medium and nystatin treatment, and less than 7% of genes that exhibit a significant increase in messenger RNA expression are also required for optimal Growth in four of the tested conditions.
Journal ArticleDOI

The Transcriptome of the Intraerythrocytic Developmental Cycle of Plasmodium falciparum

TL;DR: Analysis of the complete asexual intraerythrocytic developmental cycle (IDC) transcriptome of the HB3 strain of P. falciparum demonstrates that this parasite has evolved an extremely specialized mode of transcriptional regulation that produces a continuous cascade of gene expression, beginning with genes corresponding to general cellular processes, such as protein synthesis, and ending with Plasmodium-specific functionalities.
Journal ArticleDOI

The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of plasmodium falciparum-infected erythrocytes

TL;DR: A large and extremely diverse family of P. falciparum genes (var) that encode 200-350 kDa proteins having the expected properties of antigenically variant adhesion molecules are described.
Journal ArticleDOI

Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes

TL;DR: The cloning of two related PfEMP1 genes from the Malayan Camp parasite strain are described and the molecular basis for antigenic variation in malaria and adherence of infected erythrocytes to host cells can now be pursued.
Journal ArticleDOI

Switches in expression of Plasmodium falciparum var genes correlate with changes in antigenic and cytoadherent phenotypes of infected erythrocytes.

TL;DR: It is shown that expression of variant antigenic determinants is correlated with expression of individual members of a large, multigene family named var, which is consistent with the involvement of var genes in antigenic variation and binding to endothelium.
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