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Metacaspases-Like Proteases of Trichomonas vaginalis: In Silico Identification and Characterization
Julio César Torres-Romero1, María Elizbeth Alvarez-Sánchez2, Marcos Morales-Reyna2
1Laboratorio de Bioquímica y Genética Molecular, Facultad de Química, Universidad Autónoma de Yucatán, Mérida, Yucatán, México.
Abstract:
Metacaspases (MCA), are cysteine-dependent proteases closely related to caspases. In protozoa, MCA plays an important role in programmed cell death (PCD). In Trichomonas vaginalis, a kind of PCD that resembles apoptosis has been described, but the activators of this mechanism have not been demonstrated. We performed a genome-wide in silico analysis in the T. vaginalis database using consensus MCA domains. A total of 15 protein annotations for MCA-like sequences were retrieved. Only 7/15 (TvMCA1-6 and TvMCA9) of the sequences were annotated as putative MCA and exhibited a similar range of amino acid length in comparison to the consensus sequences used for the query. By in silico analysis, we found that they are thermostable, hydrophilic proteins with molecular weights ranging from 27 to 33 KDa and their theoretical isoelectric points are in a 5.08-8.57 range. The phylogenetic analysis showed the similarity of conserved motifs for the predicted TvMCA proteins. 3D structure prediction by homology modeling demonstrated that TvMCA proteins show a similar conformation to crystallized MCA proteins. Taken together, our results indicate that these trichomonad proteins have conserved sequences like MCA proteins and suggest that they may be responsible for proteolytic activity during a PCD-like mechanism in this parasite.
Insights
Metacaspases (MCA) are key proteases in protozoan programmed cell death (PCD). This study identified and characterized seven putative MCA proteins in Trichomonas vaginalis, suggesting their role in PCD-like mechanisms.
Area of Science:
- Molecular Biology
- Parasitology
- Biochemistry
Background:
- Metacaspases (MCA) are cysteine-dependent proteases homologous to caspases.
- MCAs are crucial for programmed cell death (PCD) in protozoa.
- The specific activators of PCD in Trichomonas vaginalis remain largely unknown.
Purpose of the Study:
- To identify and characterize metacaspase-like proteins in Trichomonas vaginalis.
- To investigate the potential role of these proteins in PCD-like processes within the parasite.
Main Methods:
- Genome-wide in silico analysis of the T. vaginalis database using MCA consensus domains.
- Phylogenetic analysis of identified MCA sequences.
- 3D structure prediction using homology modeling.
Main Results:
- Seven putative MCA sequences (TvMCA1-6 and TvMCA9) were identified from 15 annotations.
- TvMCA proteins are predicted to be thermostable, hydrophilic, with molecular weights of 27-33 KDa and pIs ranging from 5.08-8.57.
- Phylogenetic and structural analyses indicated conserved motifs and conformations similar to known MCA proteins.
Conclusions:
- Trichomonas vaginalis possesses MCA proteins with conserved sequences and structures.
- These TvMCA proteins are likely responsible for proteolytic activity in a PCD-like pathway in this parasite.
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