Literature DB >> 15463722

Secretory transport in Plasmodium.

H G Elmendorf1, K Haldar.   

Abstract

The asexual blood stage of the human malaria parasite Plasmodium falciparum resides within the mature erythrocyte - a cell that has no intracellular organelles and few biosynthetic activities. However, Plasmodium, as on actively growing and dividing cell, has numerous requirements for the uptake o f nutrients and expulsion of waste. Hence, the parasite must extensively remodel the erythrocyte to facilitate its survival, not only by exporting numerous proteins, but also by providing the requisite machinery for their .trafficking. In this review, Heidi Elmendorf and Kastun Haldar propose a model for secretion in P. falciparum.

Entities:  

Year:  1993        PMID: 15463722     DOI: 10.1016/0169-4758(93)90216-3

Source DB:  PubMed          Journal:  Parasitol Today        ISSN: 0169-4758


  18 in total

1.  In vitro biosynthesis and in vivo processing of the major microneme antigen of Sarcocystis muris cyst merozoites.

Authors:  H Klein; H Mehlhorn; W Rüger
Journal:  Parasitol Res       Date:  1996       Impact factor: 2.289

2.  The antibiotic micrococcin is a potent inhibitor of growth and protein synthesis in the malaria parasite.

Authors:  M J Rogers; E Cundliffe; T F McCutchan
Journal:  Antimicrob Agents Chemother       Date:  1998-03       Impact factor: 5.191

3.  PI(3)P-independent and -dependent pathways function together in a vacuolar translocation sequence to target malarial proteins to the host erythrocyte.

Authors:  Souvik Bhattacharjee; Kaye D Speicher; Robert V Stahelin; David W Speicher; Kasturi Haldar
Journal:  Mol Biochem Parasitol       Date:  2012-07-22       Impact factor: 1.759

4.  Endoplasmic reticulum PI(3)P lipid binding targets malaria proteins to the host cell.

Authors:  Souvik Bhattacharjee; Robert V Stahelin; Kaye D Speicher; David W Speicher; Kasturi Haldar
Journal:  Cell       Date:  2012-01-20       Impact factor: 41.582

5.  etramps, a new Plasmodium falciparum gene family coding for developmentally regulated and highly charged membrane proteins located at the parasite-host cell interface.

Authors:  Tobias Spielmann; David J P Fergusen; Hans-Peter Beck
Journal:  Mol Biol Cell       Date:  2003-04       Impact factor: 4.138

Review 6.  Parasite-regulated membrane transport processes and metabolic control in malaria-infected erythrocytes.

Authors:  B C Elford; G M Cowan; D J Ferguson
Journal:  Biochem J       Date:  1995-06-01       Impact factor: 3.857

7.  Toxoplasma invasion: the parasitophorous vacuole is formed from host cell plasma membrane and pinches off via a fission pore.

Authors:  E Suss-Toby; J Zimmerberg; G E Ward
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-06       Impact factor: 11.205

8.  Plasmodium falciparum-infected erythrocytes utilize a synthetic truncated ceramide precursor for synthesis and secretion of truncated sphingomyelin.

Authors:  I Ansorge; D Jeckel; F Wieland; K Lingelbach
Journal:  Biochem J       Date:  1995-05-15       Impact factor: 3.857

9.  In vivo activity of ajoene against rodent malaria.

Authors:  H A Perez; M De la Rosa; R Apitz
Journal:  Antimicrob Agents Chemother       Date:  1994-02       Impact factor: 5.191

10.  Biosynthesis, export and processing of a 45 kDa protein detected in membrane clefts of erythrocytes infected with Plasmodium falciparum.

Authors:  A Das; H G Elmendorf; W I Li; K Haldar
Journal:  Biochem J       Date:  1994-09-01       Impact factor: 3.857

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