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Homologous Expression of Glycosylphosphatidylinositol-Anchored Glycoproteins in Trypanosoma cruzi.
Balouz, Virginia; Mesias, Andrea C; Camean, Camila Centeno; Ducrey, Ivana; Lobo, Maite Mabel; Durante, Ignacio M; Cánepa, Gaspar E; Buscaglia, Carlos A; de Los Milagros Cámara, María.
Affiliation
  • Balouz V; Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín (UNSAM), Buenos Aires, Argentina.
  • Mesias AC; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
  • Camean CC; Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín (UNSAM), Buenos Aires, Argentina.
  • Ducrey I; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
  • Lobo MM; Instituto de Patología Experimental, CONICET, Universidad Nacional de Salta, Salta-Capital, Argentina.
  • Durante IM; Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín (UNSAM), Buenos Aires, Argentina.
  • Cánepa GE; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
  • Buscaglia CA; Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín (UNSAM), Buenos Aires, Argentina.
  • de Los Milagros Cámara M; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
Methods Mol Biol ; 1955: 119-134, 2019.
Article in En | MEDLINE | ID: mdl-30868523
The surface coat of Trypanosoma cruzi is covered with glycosylphosphatidylinositol (GPI)-anchored glycoproteins (GAGPs) that contribute to parasite protection and to the establishment of a persistent infection in both the insect vector and the mammalian host. Multiple GAGPs that vary by amino acid sequence and/or posttranslational modifications are co-expressed on the parasite surface coat, hence curtailing structural/functional analyses on these molecules. Studies in our lab have indicated that GAGP-tagged variants expressed by transfected parasites undergo analogous posttranslational processing than endogenous ones and therefore constitute suitable tools to overcome these limitations. In this chapter, we detail the entire methodological pipeline for the efficient homologous expression of GAGPs in T. cruzi: from a simple strategy for the simultaneously cloning and tagging of the gene of interest to the biochemical validation of the parasite-expressed product.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trypanosoma cruzi / Protozoan Proteins / GPI-Linked Proteins Limits: Humans Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: Argentina Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trypanosoma cruzi / Protozoan Proteins / GPI-Linked Proteins Limits: Humans Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: Argentina Country of publication: United States