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Delivery of Antisense DNA into Pathogenic Parasite Trypanosoma cruzi Using Virus-Like Protein-Based Nanoparticles.
Cárdenas-Guerra, Rosa E; Moreno-Gutierrez, David S; Vargas-Dorantes, Oscar de J; Espinoza, Bertha; Hernandez-Garcia, Armando.
Afiliación
  • Cárdenas-Guerra RE; Laboratorio de Estudios sobre Tripanosomiasis, Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México.
  • Moreno-Gutierrez DS; Laboratory of Biomolecular Engineering and Bionanotechnology, Departamento de Biomacromoléculas, Instituto de Química, Universidad Nacional Autónoma de México, Ciudad de México, México.
  • Vargas-Dorantes OJ; Laboratory of Biomolecular Engineering and Bionanotechnology, Departamento de Biomacromoléculas, Instituto de Química, Universidad Nacional Autónoma de México, Ciudad de México, México.
  • Espinoza B; Laboratorio de Estudios sobre Tripanosomiasis, Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México.
  • Hernandez-Garcia A; Laboratory of Biomolecular Engineering and Bionanotechnology, Departamento de Biomacromoléculas, Instituto de Química, Universidad Nacional Autónoma de México, Ciudad de México, México.
Nucleic Acid Ther ; 30(6): 392-401, 2020 12.
Article en En | MEDLINE | ID: mdl-32907491
ABSTRACT
Trypanosoma cruzi, which causes Chagas disease, is one of the most lacerating parasites in terms of health and social impacts. New approaches for its study and treatment are urgently needed since in more than 50 years only two drugs have been approved. Genetic approaches based on antisense oligonucleotides (AONs) are promising; however, to harness their full potential the development of effective carriers is paramount. Here, we report the use of an engineered virus-like protein C-BK12 to transfect AONs into T. cruzi. Using gel electrophoresis, Dynamic Light Scattering, and atomic force microscopy, we found that C-BK12 binds AONs and forms 10-25 nm nanoparticles (NPs), which are very stable when incubated in biological media, only releasing up to 25% of AON. Fluorescence microscopy and qPCR revealed that the NPs successfully delivered AONs into epimastigotes and reduced the expression of a target gene down to 68%. Importantly, the protein did not show cytotoxicity. The combination of high stability and capability to transfect and knock down gene expression without causing cell damage and death makes the protein C-BK12 a promising starting point for the further development of safe and effective carriers to deliver AONs into T. cruzi for biological studies.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trypanosoma cruzi / ADN sin Sentido / Enfermedad de Chagas / Nanopartículas Límite: Animals / Humans Idioma: En Revista: Nucleic Acid Ther Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trypanosoma cruzi / ADN sin Sentido / Enfermedad de Chagas / Nanopartículas Límite: Animals / Humans Idioma: En Revista: Nucleic Acid Ther Año: 2020 Tipo del documento: Article