Literature DB >> 17381432

Quantitative pH measurements in Plasmodium falciparum-infected erythrocytes using pHluorin.

Yvonne Kuhn1, Petra Rohrbach, Michael Lanzer.   

Abstract

The digestive vacuole of the malaria parasite Plasmodium falciparum is the site of action of several antimalarial drugs, such as chloroquine, which accumulate in this organelle due to their properties as amphiphilic weak bases that inhibit haem detoxification. It has been suggested that changes in the pH of the digestive vacuole, affecting either drug partitioning or haem solubility and/or biomineralization rates, would correlate with reduced intracellular chloroquine accumulation and, hence, would determine the chloroquine-resistance phenotype. The techniques previously used to quantify digestive vacuolar pH mainly relied on lysed or isolated parasites, with unpredictable consequences on internal pH homeostasis. In this study, we have investigated the baseline steady-state pH of the cytoplasm and digestive vacuole of a chloroquine-sensitive (HB3) and a chloroquine-resistant (Dd2) parasite using a pH-sensitive green fluorescent protein, termed pHluorin. This non-invasive technique allows for in vivo pH measurements in intact P. falciparum-infected erythrocytes under physiological conditions. The data suggest that the pH of the cytoplasm is approximately 7.15 +/- 0.07 and that of the digestive vacuole approximately 5.18 +/- 0.05. No significant differences in baseline pH values were recorded for the chloroquine-sensitive and chloroquine-resistant parasites.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17381432     DOI: 10.1111/j.1462-5822.2006.00847.x

Source DB:  PubMed          Journal:  Cell Microbiol        ISSN: 1462-5814            Impact factor:   3.715


  41 in total

Review 1.  Know your enemy: understanding the role of PfCRT in drug resistance could lead to new antimalarial tactics.

Authors:  Robert L Summers; Megan N Nash; Rowena E Martin
Journal:  Cell Mol Life Sci       Date:  2012-06       Impact factor: 9.261

2.  Differences in trans-stimulated chloroquine efflux kinetics are linked to PfCRT in Plasmodium falciparum.

Authors:  Cecilia P Sanchez; Petra Rohrbach; Jeremy E McLean; David A Fidock; Wilfred D Stein; Michael Lanzer
Journal:  Mol Microbiol       Date:  2007-04       Impact factor: 3.501

3.  Distribution and biochemical properties of an M1-family aminopeptidase in Plasmodium falciparum indicate a role in vacuolar hemoglobin catabolism.

Authors:  Daniel Ragheb; Seema Dalal; Kristin M Bompiani; W Keith Ray; Michael Klemba
Journal:  J Biol Chem       Date:  2011-06-09       Impact factor: 5.157

4.  Engagement of the S1, S1' and S2' subsites drives efficient catalysis of peptide bond hydrolysis by the M1-family aminopeptidase from Plasmodium falciparum.

Authors:  Seema Dalal; Daniel R T Ragheb; Michael Klemba
Journal:  Mol Biochem Parasitol       Date:  2012-02-13       Impact factor: 1.759

Review 5.  PfCRT and its role in antimalarial drug resistance.

Authors:  Andrea Ecker; Adele M Lehane; Jérôme Clain; David A Fidock
Journal:  Trends Parasitol       Date:  2012-09-25

6.  Analysis of chloroquine resistance transporter (CRT) isoforms and orthologues in S. cerevisiae yeast.

Authors:  Nicholas K Baro; Chaya Pooput; Paul D Roepe
Journal:  Biochemistry       Date:  2011-07-19       Impact factor: 3.162

7.  Chloroquine resistance-conferring mutations in pfcrt give rise to a chloroquine-associated H+ leak from the malaria parasite's digestive vacuole.

Authors:  Adele M Lehane; Kiaran Kirk
Journal:  Antimicrob Agents Chemother       Date:  2008-10-13       Impact factor: 5.191

8.  On the mechanism of chloroquine resistance in Plasmodium falciparum.

Authors:  Mauro Chinappi; Allegra Via; Paolo Marcatili; Anna Tramontano
Journal:  PLoS One       Date:  2010-11-19       Impact factor: 3.240

9.  Evidence for catalytic roles for Plasmodium falciparum aminopeptidase P in the food vacuole and cytosol.

Authors:  Daniel Ragheb; Kristin Bompiani; Seema Dalal; Michael Klemba
Journal:  J Biol Chem       Date:  2009-07-02       Impact factor: 5.157

10.  Hemoglobin cleavage site-specificity of the Plasmodium falciparum cysteine proteases falcipain-2 and falcipain-3.

Authors:  Shoba Subramanian; Markus Hardt; Youngchool Choe; Richard K Niles; Eric B Johansen; Jennifer Legac; Jiri Gut; Iain D Kerr; Charles S Craik; Philip J Rosenthal
Journal:  PLoS One       Date:  2009-04-09       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.