Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target

The primary effector of cGMP signaling in Plasmodium is the cGMP-dependent protein kinase (PKG). Work in human-infective Plasmodium falciparum and rodent-infective Plasmodium berghei has provided biological validation of P. falciparum PKG (PfPKG) as a drug target for treating and/or protecting again...

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Main Authors: David Rotella, John Siekierka, Purnima Bhanot
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2020.610408/full
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spelling doaj-bdc2d2f5c84f44a890a477d0bd24f4f22021-02-03T04:24:01ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2021-02-011110.3389/fmicb.2020.610408610408Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic TargetDavid Rotella0John Siekierka1Purnima Bhanot2Department of Chemistry and Biochemistry, Montclair State University, Montclair, NJ, United StatesDepartment of Chemistry and Biochemistry, Montclair State University, Montclair, NJ, United StatesDepartment of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, NJ, United StatesThe primary effector of cGMP signaling in Plasmodium is the cGMP-dependent protein kinase (PKG). Work in human-infective Plasmodium falciparum and rodent-infective Plasmodium berghei has provided biological validation of P. falciparum PKG (PfPKG) as a drug target for treating and/or protecting against malaria. PfPKG is essential in the asexual erythrocytic and sexual cycles as well as the pre-erythrocytic cycle. Medicinal chemistry efforts, both target-based and phenotype-based, have targeted PfPKG in the past few years. This review provides a brief overview of their results and challenges.https://www.frontiersin.org/articles/10.3389/fmicb.2020.610408/fullPlasmodiummalariacGMP signalingsecond messengerkinase
collection DOAJ
language English
format Article
sources DOAJ
author David Rotella
John Siekierka
Purnima Bhanot
spellingShingle David Rotella
John Siekierka
Purnima Bhanot
Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
Frontiers in Microbiology
Plasmodium
malaria
cGMP signaling
second messenger
kinase
author_facet David Rotella
John Siekierka
Purnima Bhanot
author_sort David Rotella
title Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
title_short Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
title_full Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
title_fullStr Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
title_full_unstemmed Plasmodium falciparum cGMP-Dependent Protein Kinase – A Novel Chemotherapeutic Target
title_sort plasmodium falciparum cgmp-dependent protein kinase – a novel chemotherapeutic target
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2021-02-01
description The primary effector of cGMP signaling in Plasmodium is the cGMP-dependent protein kinase (PKG). Work in human-infective Plasmodium falciparum and rodent-infective Plasmodium berghei has provided biological validation of P. falciparum PKG (PfPKG) as a drug target for treating and/or protecting against malaria. PfPKG is essential in the asexual erythrocytic and sexual cycles as well as the pre-erythrocytic cycle. Medicinal chemistry efforts, both target-based and phenotype-based, have targeted PfPKG in the past few years. This review provides a brief overview of their results and challenges.
topic Plasmodium
malaria
cGMP signaling
second messenger
kinase
url https://www.frontiersin.org/articles/10.3389/fmicb.2020.610408/full
work_keys_str_mv AT davidrotella plasmodiumfalciparumcgmpdependentproteinkinaseanovelchemotherapeutictarget
AT johnsiekierka plasmodiumfalciparumcgmpdependentproteinkinaseanovelchemotherapeutictarget
AT purnimabhanot plasmodiumfalciparumcgmpdependentproteinkinaseanovelchemotherapeutictarget
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