The Diverse Calpain Family in Trypanosomatidae: Functional Proteins Devoid of Proteolytic Activity?
Calpains are calcium-dependent cysteine peptidases that were originally described in mammals and, thereafter, their homologues were identified in almost all known living organisms. The deregulated activity of these peptidases is associated with several pathologies and, consequently, huge efforts hav...
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Published in | Cells (Basel, Switzerland) Vol. 10; no. 2; p. 299 |
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Abstract | Calpains are calcium-dependent cysteine peptidases that were originally described in mammals and, thereafter, their homologues were identified in almost all known living organisms. The deregulated activity of these peptidases is associated with several pathologies and, consequently, huge efforts have been made to identify selective inhibitors. Trypanosomatids, responsible for life-threatening human diseases, possess a large and diverse family of calpain sequences in their genomes. Considering that the current therapy to treat trypanosomatid diseases is limited to a handful of drugs that suffer from unacceptable toxicity, tough administration routes, like parenteral, and increasing treatment failures, a repurposed approach with calpain inhibitors could be a shortcut to successful chemotherapy. However, there is a general lack of knowledge about calpain functions in these parasites and, currently, the proteolytic activity of these proteins is still an open question. Here, we highlight the current research and perspectives on trypanosomatid calpains, overview calpain description in these organisms, and explore the potential of targeting the calpain system as a therapeutic strategy. This review gathers the current knowledge about this fascinating family of peptidases as well as insights into the puzzle: are we unable to measure calpain activity in trypanosomatids, or are the functions of these proteins devoid of proteolytic activity in these parasites? |
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AbstractList | Calpains are calcium-dependent cysteine peptidases that were originally described in mammals and, thereafter, their homologues were identified in almost all known living organisms. The deregulated activity of these peptidases is associated with several pathologies and, consequently, huge efforts have been made to identify selective inhibitors. Trypanosomatids, responsible for life-threatening human diseases, possess a large and diverse family of calpain sequences in their genomes. Considering that the current therapy to treat trypanosomatid diseases is limited to a handful of drugs that suffer from unacceptable toxicity, tough administration routes, like parenteral, and increasing treatment failures, a repurposed approach with calpain inhibitors could be a shortcut to successful chemotherapy. However, there is a general lack of knowledge about calpain functions in these parasites and, currently, the proteolytic activity of these proteins is still an open question. Here, we highlight the current research and perspectives on trypanosomatid calpains, overview calpain description in these organisms, and explore the potential of targeting the calpain system as a therapeutic strategy. This review gathers the current knowledge about this fascinating family of peptidases as well as insights into the puzzle: are we unable to measure calpain activity in trypanosomatids, or are the functions of these proteins devoid of proteolytic activity in these parasites? |
Author | Ennes-Vidal, Vítor Branquinha, Marta Helena d'Avila-Levy, Claudia Masini Dos Santos, André Luis Souza |
AuthorAffiliation | 2 Laboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro (UFRJ), 21941-901 Rio de Janeiro, Brazil; mbranquinha@micro.ufrj.br (M.H.B.); andre@micro.ufrj.br (A.L.S.d.S.) 3 Programa de Pós-Graduação em Bioquímica, Instituto de Química, Universidade Federal do Rio de Janeiro (UFRJ), 21941-909 Rio de Janeiro, Brazil 1 Laboratório de Estudos Integrados em Protozoologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), 21040-360 Rio de Janeiro, Brazil; davila.levy@ioc.fiocruz.br |
AuthorAffiliation_xml | – name: 3 Programa de Pós-Graduação em Bioquímica, Instituto de Química, Universidade Federal do Rio de Janeiro (UFRJ), 21941-909 Rio de Janeiro, Brazil – name: 1 Laboratório de Estudos Integrados em Protozoologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), 21040-360 Rio de Janeiro, Brazil; davila.levy@ioc.fiocruz.br – name: 2 Laboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro (UFRJ), 21941-901 Rio de Janeiro, Brazil; mbranquinha@micro.ufrj.br (M.H.B.); andre@micro.ufrj.br (A.L.S.d.S.) |
Author_xml | – sequence: 1 givenname: Vítor orcidid: 0000-0001-6122-1956 surname: Ennes-Vidal fullname: Ennes-Vidal, Vítor organization: Laboratório de Estudos Integrados em Protozoologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), 21040-360 Rio de Janeiro, Brazil – sequence: 2 givenname: Marta Helena orcidid: 0000-0002-9752-8148 surname: Branquinha fullname: Branquinha, Marta Helena organization: Laboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro (UFRJ), 21941-901 Rio de Janeiro, Brazil – sequence: 3 givenname: André Luis Souza orcidid: 0000-0003-0821-8592 surname: Dos Santos fullname: Dos Santos, André Luis Souza organization: Programa de Pós-Graduação em Bioquímica, Instituto de Química, Universidade Federal do Rio de Janeiro (UFRJ), 21941-909 Rio de Janeiro, Brazil – sequence: 4 givenname: Claudia Masini orcidid: 0000-0001-8042-4695 surname: d'Avila-Levy fullname: d'Avila-Levy, Claudia Masini organization: Laboratório de Estudos Integrados em Protozoologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), 21040-360 Rio de Janeiro, Brazil |
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CitedBy_id | crossref_primary_10_1590_0074_02760220017 crossref_primary_10_3389_fmolb_2023_1191934 crossref_primary_10_3390_tropicalmed7020029 crossref_primary_10_1208_s12249_022_02247_3 |
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Keywords | Trypanosoma cysteine peptidase chemotherapy Leishmania |
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SubjectTerms | Calcium Calpain Cell division Chagas disease Chemotherapy Coronaviruses cysteine peptidase Drug dosages Gene expression Genomes Leishmania Mammals Parasites Parasitic diseases Proteins Proteolysis Review Toxicity Tropical diseases Trypanosoma Virulence |
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Title | The Diverse Calpain Family in Trypanosomatidae: Functional Proteins Devoid of Proteolytic Activity? |
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