Evidence of G-Protein-Coupled Receptors (GPCR) in the Parasitic Protozoa Plasmodium falciparum-Sensing the Host Environment and Coupling within Its Molecular Signaling Toolkit
- PMID: 34830263
- PMCID: PMC8620569
- DOI: 10.3390/ijms222212381
Evidence of G-Protein-Coupled Receptors (GPCR) in the Parasitic Protozoa Plasmodium falciparum-Sensing the Host Environment and Coupling within Its Molecular Signaling Toolkit
Abstract
Throughout evolution, the need for single-celled organisms to associate and form a single cluster of cells has had several evolutionary advantages. In complex, multicellular organisms, each tissue or organ has a specialty and function that make life together possible, and the organism as a whole needs to act in balance and adapt to changes in the environment. Sensory organs are essential for connecting external stimuli into a biological response, through the senses: sight, smell, taste, hearing, and touch. The G-protein-coupled receptors (GPCRs) are responsible for many of these senses and therefore play a key role in the perception of the cells' external environment, enabling interaction and coordinated development between each cell of a multicellular organism. The malaria-causing protozoan parasite, Plasmodium falciparum, has a complex life cycle that is extremely dependent on a finely regulated cellular signaling machinery. In this review, we summarize strong evidence and the main candidates of GPCRs in protozoan parasites. Interestingly, one of these GPCRs is a sensor for K+ shift in Plasmodium falciparum, PfSR25. Studying this family of proteins in P. falciparum could have a significant impact, both on understanding the history of the evolution of GPCRs and on finding new targets for antimalarials.
Keywords: GPCRs; Plasmodium falciparum; calcium; cell signaling; synchronization.
Conflict of interest statement
The authors declare no conflict of interest.
Figures

Similar articles
-
Identifying Plasmodium falciparum receptor activation using bioluminescence resonance energy transfer (BRET)-based biosensors in HEK293 cells.Methods Cell Biol. 2021;166:223-233. doi: 10.1016/bs.mcb.2021.06.018. Epub 2021 Aug 7. Methods Cell Biol. 2021. PMID: 34752334
-
Plasmodium falciparum GPCR-like receptor SR25 mediates extracellular K+ sensing coupled to Ca2+ signaling and stress survival.Sci Rep. 2017 Aug 25;7(1):9545. doi: 10.1038/s41598-017-09959-8. Sci Rep. 2017. PMID: 28842684 Free PMC article.
-
Antimalarial and Plasmodium falciparum serpentine receptor 12 targeting effect of FDA approved purinergic receptor antagonist.J Biomol Struct Dyn. 2023 Nov;41(19):9462-9475. doi: 10.1080/07391102.2022.2142298. Epub 2022 Nov 9. J Biomol Struct Dyn. 2023. PMID: 36351236
-
A proteomic glimpse into the effect of antimalarial drugs on Plasmodium falciparum proteome towards highlighting possible therapeutic targets.Pathog Dis. 2021 Jan 9;79(1):ftaa071. doi: 10.1093/femspd/ftaa071. Pathog Dis. 2021. PMID: 33202000 Review.
-
Evidences of G Coupled-Protein Receptor (GPCR) Signaling in the human Malaria Parasite Plasmodium falciparum for Sensing its Microenvironment and the Role of Purinergic Signaling in Malaria Parasites.Curr Top Med Chem. 2021;21(3):171-180. doi: 10.2174/1568026620666200826122716. Curr Top Med Chem. 2021. PMID: 32851963 Review.
Cited by
-
Molecular Characterization and Expression Analysis of Putative Class C (Glutamate Family) G Protein-Coupled Receptors in Ascidian Styela clava.Biology (Basel). 2022 May 20;11(5):782. doi: 10.3390/biology11050782. Biology (Basel). 2022. PMID: 35625509 Free PMC article.
-
Genome-wide identification and functional characterization of GPCR family genes reveal their key roles in the vitellarium development and egg production in Schistosoma japonicum.Parasit Vectors. 2025 Jul 17;18(1):286. doi: 10.1186/s13071-025-06929-2. Parasit Vectors. 2025. PMID: 40676690 Free PMC article.
-
G Protein-Coupled Receptors as Potential Intercellular Communication Mediators in Trypanosomatidae.Front Cell Infect Microbiol. 2022 May 16;12:812848. doi: 10.3389/fcimb.2022.812848. eCollection 2022. Front Cell Infect Microbiol. 2022. PMID: 35651757 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources