Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/83602
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Malaria parasite signal peptide peptidase is an ER-resident protease required for growth but not for invasion
Author: Marapana, D.
Wilson, D.
Zuccala, E.
Dekiwadia, C.
Beeson, J.
Ralph, S.
Baum, J.
Citation: Traffic, 2012; 13(11):1457-1465
Publisher: Munksgaard Int Publ Ltd
Issue Date: 2012
ISSN: 1398-9219
1600-0854
Statement of
Responsibility: 
Danushka S. Marapana, Danny W. Wilson, Elizabeth S. Zuccala, Chaitali D. Dekiwadia, James G. Beeson, Stuart A. Ralph and Jake Baum
Abstract: The establishment of parasite infection within the human erythrocyte is an essential stage in the development of malaria disease. As such, significant interest has focused on the mechanics that underpin invasion and on characterization of parasite molecules involved. Previous evidence has implicated a presenilin-like signal peptide peptidase (SPP) from the most virulent human malaria parasite, Plasmodium falciparum, in the process of invasion where it has been proposed to function in the cleavage of the erythrocyte cytoskeletal protein Band 3. The role of a traditionally endoplasmic reticulum (ER) protease in the process of red blood cell invasion is unexpected. Here, using a combination of molecular, cellular and chemical approaches we provide evidence that PfSPP is, instead, a bona fide ER-resident peptidase that remains intracellular throughout the invasion process. Furthermore, SPP-specific drug inhibition has no effect on erythrocyte invasion whilst having low micromolar potency against intra-erythrocytic development. Contrary to previous reports, these results show that PfSPP plays no role in erythrocyte invasion. Nonetheless, PfSPP clearly represents a potential chemotherapeutic target to block parasite growth, supporting ongoing efforts to develop antimalarial-targeting protein maturation and trafficking during intra-erythrocytic development.
Keywords: endoplasmic reticulum; gamma-secretase; malaria; merozoite; microneme; Plasmodium falciparum; presenilin; signal peptide peptidase; tight junction
Rights: © 2012 John Wiley & Sons A/S
RMID: 0020138029
DOI: 10.1111/j.1600-0854.2012.01402.x
Appears in Collections:Molecular and Biomedical Science publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.