A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi
- Autores
- Perrone, Alina Elizabeth; Milduberger, Natalia Ayelen; Fuchs, Alicia Graciela; Bustos, Patricia Laura; Bua, Jacqueline Elena
- Año de publicación
- 2018
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Trypanosoma cruzi is the etiological agent of Chagas disease. It affects eight million people worldwide and can be spread by several routes, such as vectorborne transmission in endemic areas and congenitally, and is also important in non-endemic regions such as the United States and Europe due to migration from Latin America. Cyclophilins (CyPs) are proteins with enzymatic peptidyl-prolyl isomerase activity (PPIase), essential for protein folding in vivo. Cyclosporin A (CsA) has a high binding affinity for CyPs and inhibits their PPIase activity. CsA has proved to be a parasiticidal drug on some protozoa, including T. cruzi. In this review, we describe the T. cruzi cyclophilin gene family, that comprises 15 paralogues. Among the proteins isolated by CsA-affinity chromatography, we found orthologues of mammalian CyPs. TcCyP19, as the human CyPA, is secreted to the extracellular environment by all parasite stages and could be part of a complex interplay involving the parasite and the host cell. TcCyP22, an orthologue of mitochondrial CyPD, is involved in the regulation of parasite cell death. Our findings on T. cruzi cyclophilins will allow further characterization of these processes, leading to new insights into the biology, the evolution of metabolic pathways, and novel targets for anti-T. cruzi control.
Fil: Perrone, Alina Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina
Fil: Milduberger, Natalia Ayelen. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Abierta Interamericana; Argentina
Fil: Fuchs, Alicia Graciela. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; Argentina
Fil: Bustos, Patricia Laura. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bua, Jacqueline Elena. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
CELL DEATH
CHAGAS DISEASE
CYCLOPHILINS
CYCLOSPORIN A
NON-IMMUNO SUPPRESSIVE ANALOGS
PROTOZOAN PARASITE
TCCYP19
TCCYP22
TRYPANOCIDAL COMPOUNDS
TRYPANOSOMA CRUZI - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/162278
Ver los metadatos del registro completo
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A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruziPerrone, Alina ElizabethMilduberger, Natalia AyelenFuchs, Alicia GracielaBustos, Patricia LauraBua, Jacqueline ElenaCELL DEATHCHAGAS DISEASECYCLOPHILINSCYCLOSPORIN ANON-IMMUNO SUPPRESSIVE ANALOGSPROTOZOAN PARASITETCCYP19TCCYP22TRYPANOCIDAL COMPOUNDSTRYPANOSOMA CRUZIhttps://purl.org/becyt/ford/3.4https://purl.org/becyt/ford/3Trypanosoma cruzi is the etiological agent of Chagas disease. It affects eight million people worldwide and can be spread by several routes, such as vectorborne transmission in endemic areas and congenitally, and is also important in non-endemic regions such as the United States and Europe due to migration from Latin America. Cyclophilins (CyPs) are proteins with enzymatic peptidyl-prolyl isomerase activity (PPIase), essential for protein folding in vivo. Cyclosporin A (CsA) has a high binding affinity for CyPs and inhibits their PPIase activity. CsA has proved to be a parasiticidal drug on some protozoa, including T. cruzi. In this review, we describe the T. cruzi cyclophilin gene family, that comprises 15 paralogues. Among the proteins isolated by CsA-affinity chromatography, we found orthologues of mammalian CyPs. TcCyP19, as the human CyPA, is secreted to the extracellular environment by all parasite stages and could be part of a complex interplay involving the parasite and the host cell. TcCyP22, an orthologue of mitochondrial CyPD, is involved in the regulation of parasite cell death. Our findings on T. cruzi cyclophilins will allow further characterization of these processes, leading to new insights into the biology, the evolution of metabolic pathways, and novel targets for anti-T. cruzi control.Fil: Perrone, Alina Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; ArgentinaFil: Milduberger, Natalia Ayelen. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Abierta Interamericana; ArgentinaFil: Fuchs, Alicia Graciela. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; ArgentinaFil: Bustos, Patricia Laura. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Bua, Jacqueline Elena. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaMDPI AG2018-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/162278Perrone, Alina Elizabeth; Milduberger, Natalia Ayelen; Fuchs, Alicia Graciela; Bustos, Patricia Laura; Bua, Jacqueline Elena; A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi; MDPI AG; Biomolecules; 8; 4; 10-2018; 1-92218-273XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.3390/biom8040132info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:23:17Zoai:ri.conicet.gov.ar:11336/162278instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-05 10:23:17.537CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| title |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| spellingShingle |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi Perrone, Alina Elizabeth CELL DEATH CHAGAS DISEASE CYCLOPHILINS CYCLOSPORIN A NON-IMMUNO SUPPRESSIVE ANALOGS PROTOZOAN PARASITE TCCYP19 TCCYP22 TRYPANOCIDAL COMPOUNDS TRYPANOSOMA CRUZI |
| title_short |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| title_full |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| title_fullStr |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| title_full_unstemmed |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| title_sort |
A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi |
| dc.creator.none.fl_str_mv |
Perrone, Alina Elizabeth Milduberger, Natalia Ayelen Fuchs, Alicia Graciela Bustos, Patricia Laura Bua, Jacqueline Elena |
| author |
Perrone, Alina Elizabeth |
| author_facet |
Perrone, Alina Elizabeth Milduberger, Natalia Ayelen Fuchs, Alicia Graciela Bustos, Patricia Laura Bua, Jacqueline Elena |
| author_role |
author |
| author2 |
Milduberger, Natalia Ayelen Fuchs, Alicia Graciela Bustos, Patricia Laura Bua, Jacqueline Elena |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
CELL DEATH CHAGAS DISEASE CYCLOPHILINS CYCLOSPORIN A NON-IMMUNO SUPPRESSIVE ANALOGS PROTOZOAN PARASITE TCCYP19 TCCYP22 TRYPANOCIDAL COMPOUNDS TRYPANOSOMA CRUZI |
| topic |
CELL DEATH CHAGAS DISEASE CYCLOPHILINS CYCLOSPORIN A NON-IMMUNO SUPPRESSIVE ANALOGS PROTOZOAN PARASITE TCCYP19 TCCYP22 TRYPANOCIDAL COMPOUNDS TRYPANOSOMA CRUZI |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.4 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
Trypanosoma cruzi is the etiological agent of Chagas disease. It affects eight million people worldwide and can be spread by several routes, such as vectorborne transmission in endemic areas and congenitally, and is also important in non-endemic regions such as the United States and Europe due to migration from Latin America. Cyclophilins (CyPs) are proteins with enzymatic peptidyl-prolyl isomerase activity (PPIase), essential for protein folding in vivo. Cyclosporin A (CsA) has a high binding affinity for CyPs and inhibits their PPIase activity. CsA has proved to be a parasiticidal drug on some protozoa, including T. cruzi. In this review, we describe the T. cruzi cyclophilin gene family, that comprises 15 paralogues. Among the proteins isolated by CsA-affinity chromatography, we found orthologues of mammalian CyPs. TcCyP19, as the human CyPA, is secreted to the extracellular environment by all parasite stages and could be part of a complex interplay involving the parasite and the host cell. TcCyP22, an orthologue of mitochondrial CyPD, is involved in the regulation of parasite cell death. Our findings on T. cruzi cyclophilins will allow further characterization of these processes, leading to new insights into the biology, the evolution of metabolic pathways, and novel targets for anti-T. cruzi control. Fil: Perrone, Alina Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina Fil: Milduberger, Natalia Ayelen. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Abierta Interamericana; Argentina Fil: Fuchs, Alicia Graciela. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; Argentina Fil: Bustos, Patricia Laura. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Bua, Jacqueline Elena. Dirección Nacional de Instituto de Investigación. Administración Nacional de Laboratorio e Instituto de Salud “Dr. C. G. Malbrán”. Instituto Nacional de Parasitología "Dr. Mario Fatala Chaben”; Argentina. Universidad Abierta Interamericana; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
| description |
Trypanosoma cruzi is the etiological agent of Chagas disease. It affects eight million people worldwide and can be spread by several routes, such as vectorborne transmission in endemic areas and congenitally, and is also important in non-endemic regions such as the United States and Europe due to migration from Latin America. Cyclophilins (CyPs) are proteins with enzymatic peptidyl-prolyl isomerase activity (PPIase), essential for protein folding in vivo. Cyclosporin A (CsA) has a high binding affinity for CyPs and inhibits their PPIase activity. CsA has proved to be a parasiticidal drug on some protozoa, including T. cruzi. In this review, we describe the T. cruzi cyclophilin gene family, that comprises 15 paralogues. Among the proteins isolated by CsA-affinity chromatography, we found orthologues of mammalian CyPs. TcCyP19, as the human CyPA, is secreted to the extracellular environment by all parasite stages and could be part of a complex interplay involving the parasite and the host cell. TcCyP22, an orthologue of mitochondrial CyPD, is involved in the regulation of parasite cell death. Our findings on T. cruzi cyclophilins will allow further characterization of these processes, leading to new insights into the biology, the evolution of metabolic pathways, and novel targets for anti-T. cruzi control. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018-10 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/162278 Perrone, Alina Elizabeth; Milduberger, Natalia Ayelen; Fuchs, Alicia Graciela; Bustos, Patricia Laura; Bua, Jacqueline Elena; A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi; MDPI AG; Biomolecules; 8; 4; 10-2018; 1-9 2218-273X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/162278 |
| identifier_str_mv |
Perrone, Alina Elizabeth; Milduberger, Natalia Ayelen; Fuchs, Alicia Graciela; Bustos, Patricia Laura; Bua, Jacqueline Elena; A functional analysis of the cyclophilin repertoire in the protozoan parasite trypanosoma cruzi; MDPI AG; Biomolecules; 8; 4; 10-2018; 1-9 2218-273X CONICET Digital CONICET |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/doi/10.3390/biom8040132 |
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application/pdf application/pdf |
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MDPI AG |
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MDPI AG |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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