Patricia Ramos Guimarães
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Patricia Ramos Guimarães has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Ana Lúcia Oliveira-Carvalho
Rede Proteômica do Rio de Janeiro and Laboratório de Hemostase e Venenos, Unidade de Espectrometria de Massas e Proteômica, Instituto de Bioquímica Médica-ICB, Universidade Federal do Rio de Janeiro, Rio de Janeiro/RJ, Brazil
1 shared publicationCarlos Rangel Rodrigues
1 shared publication- Daniela Lourenço
Instituto Nacional de Metrologia, Normalização e Qualidade Industrial - INMETRO, Rio de Janeiro, Brazil.
1 shared publication Denis L.S. Dutra
1 shared publication- Helena Carla Castro
Universidade Federal Fluminense, Hospital Universitário Antônio Pedro, Programa de Pós-graduação em Patologia, 24033-900 Niterói, RJ, Brazil; Universidade Federal Fluminense, Instituto de Biologia, Programa de Pós-graduação em Ciências e Biotecnologia, CEP 24210-130, Niterói, RJ, Brazil
1 shared publication - Iamara da Silva Andrade
Instituto Nacional de Metrologia, Normalização e Qualidade Industrial - INMETRO, Rio de Janeiro, Brazil
1 shared publication
Latest Publications
- Open Access
- 19 January 2012
- Published by Springer Nature in BMC Research Notes
- Vol. 5 (1) , 41
Proteomic analysis of the ventral disc of Giardia lamblia
Background: Giardia lamblia is a multiflagellated protozoan that inhabits the small intestine of vertebrates, causing giardiasis. To colonize the small intestine, the trophozoites form of the parasite remains attached to intestinal epithelial cells by means of cytoskeletal elements that form a structure known as the ventral disc. Previous studies have shown that the ventral disc is made of tubulin and giardins. Results: To obtain further information on the composition of the ventral disc, we developed a new protocol and evaluated the purity of the isolation by transmission electron microscopy. Using 1D- and 2D-PAGE and mass spectrometry, we identified proteins with functions associated with the disc. In addition to finding tubulin and giardin, proteins known to be associated with the ventral disc, we also identified proteins annotated in the Giardia genome, but whose function was previously unknown. Conclusions: The isolation of the ventral disc shown in this work, compared to previously published protocols, proved to be more efficient. Proteomic analysis showed the presence of several proteins whose further characterization may help in the elucidation of the mechanisms involved in the attachment of the protozoan to epithelial cells.
- 19 January 2012
- Published by Springer Nature in BMC Research Notes
- Vol. 5 (1) , 41
Open AccessProteomic analysis of the ventral disc of Giardia lamblia
Background: Giardia lamblia is a multiflagellated protozoan that inhabits the small intestine of vertebrates, causing giardiasis. To colonize the small intestine, the trophozoites form of the parasite remains attached to intestinal epithelial cells by means of cytoskeletal elements that form a structure known as the ventral disc. Previous studies have shown that the ventral disc is made of tubulin and giardins. Results: To obtain further information on the composition of the ventral disc, we developed a new protocol and evaluated the purity of the isolation by transmission electron microscopy. Using 1D- and 2D-PAGE and mass spectrometry, we identified proteins with functions associated with the disc. In addition to finding tubulin and giardin, proteins known to be associated with the ventral disc, we also identified proteins annotated in the Giardia genome, but whose function was previously unknown. Conclusions: The isolation of the ventral disc shown in this work, compared to previously published protocols, proved to be more efficient. Proteomic analysis showed the presence of several proteins whose further characterization may help in the elucidation of the mechanisms involved in the attachment of the protozoan to epithelial cells.