Literature DB >> 19796339

Membrane transport proteins of the malaria parasite.

Rowena E Martin1, Hagai Ginsburg, Kiaran Kirk.   

Abstract

The malaria parasite-infected erythrocyte is a multi-compartment structure, incorporating numerous different membrane systems. The movement of nutrients, metabolites and inorganic ions into and out of the intraerythrocytic parasite, as well as between subcellular compartments within the parasite, is mediated by transporters and channels - integral membrane proteins that facilitate the movement of solutes across the membrane bilayer. Proteins of this type also play a key role in antimalarial drug resistance. Genes encoding transporters and channels account for at least 2.5% of the parasite genome. However, ascribing functions and physiological roles to these proteins, and defining their roles in drug resistance, is not straightforward. For any given membrane transport protein, a full understanding of its role(s) in the parasitized erythrocyte requires a knowledge of its subcellular localization and substrate specificity, as well as some knowledge of the effects on the parasite of modifying the sequence and/or level of expression of the gene involved. Here we consider recent work in this area, describe a number of newly identified transport proteins, and summarize the likely subcellular localization and putative substrate specificity of all of the candidate membrane transport proteins identified to date.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19796339     DOI: 10.1111/j.1365-2958.2009.06863.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  33 in total

1.  Transmembrane segment 11 appears to line the purine permeation pathway of the Plasmodium falciparum equilibrative nucleoside transporter 1 (PfENT1).

Authors:  Paul M Riegelhaupt; I J Frame; Myles H Akabas
Journal:  J Biol Chem       Date:  2010-03-24       Impact factor: 5.157

2.  Plasmodium Niemann-Pick type C1-related protein is a druggable target required for parasite membrane homeostasis.

Authors:  Eva S Istvan; Sudipta Das; Suyash Bhatnagar; Josh R Beck; Edward Owen; Manuel Llinas; Suresh M Ganesan; Jacquin C Niles; Elizabeth Winzeler; Akhil B Vaidya; Daniel E Goldberg
Journal:  Elife       Date:  2019-03-19       Impact factor: 8.140

3.  Gene selective mRNA cleavage inhibits the development of Plasmodium falciparum.

Authors:  Yoann Augagneur; Donna Wesolowski; Hyun Seop Tae; Sidney Altman; Choukri Ben Mamoun
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-02       Impact factor: 11.205

4.  Tissue expression pattern of ABCG transporter indicates functional roles in reproduction of Toxocara canis.

Authors:  Yong-Li Luo; Guang-Xu Ma; Yong-Fang Luo; Ce-Yan Kuang; Ai-Yun Jiang; Guo-Qing Li; Rong-Qiong Zhou
Journal:  Parasitol Res       Date:  2018-02-08       Impact factor: 2.289

5.  Piperaquine resistance is associated with a copy number variation on chromosome 5 in drug-pressured Plasmodium falciparum parasites.

Authors:  Richard T Eastman; Neekesh V Dharia; Elizabeth A Winzeler; David A Fidock
Journal:  Antimicrob Agents Chemother       Date:  2011-05-16       Impact factor: 5.191

Review 6.  Purine import into malaria parasites as a target for antimalarial drug development.

Authors:  I J Frame; Roman Deniskin; Avish Arora; Myles H Akabas
Journal:  Ann N Y Acad Sci       Date:  2014-11-25       Impact factor: 5.691

7.  Biosynthesis of GDP-fucose and other sugar nucleotides in the blood stages of Plasmodium falciparum.

Authors:  Sílvia Sanz; Giulia Bandini; Diego Ospina; Maria Bernabeu; Karina Mariño; Carmen Fernández-Becerra; Luis Izquierdo
Journal:  J Biol Chem       Date:  2013-04-24       Impact factor: 5.157

8.  Antimalarial drug targets in Plasmodium falciparum predicted by stage-specific metabolic network analysis.

Authors:  Carola Huthmacher; Andreas Hoppe; Sascha Bulik; Hermann-Georg Holzhütter
Journal:  BMC Syst Biol       Date:  2010-08-31

9.  Malaria parasites tolerate a broad range of ionic environments and do not require host cation remodelling.

Authors:  Ajay D Pillai; Rachel Addo; Paresh Sharma; Wang Nguitragool; Prakash Srinivasan; Sanjay A Desai
Journal:  Mol Microbiol       Date:  2013-02-26       Impact factor: 3.501

10.  Identification and functional analysis of the primary pantothenate transporter, PfPAT, of the human malaria parasite Plasmodium falciparum.

Authors:  Yoann Augagneur; Lise Jaubert; Matthieu Schiavoni; Niseema Pachikara; Aprajita Garg; Sahar Usmani-Brown; Donna Wesolowski; Skye Zeller; Abhisek Ghosal; Emmanuel Cornillot; Hamid M Said; Priti Kumar; Sidney Altman; Choukri Ben Mamoun
Journal:  J Biol Chem       Date:  2013-05-31       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.