Identification of protein complex associated with LYT1 of Trypanosoma cruzi


Por: Lugo-Caballero C., Ballesteros-Rodea G., Martínez-Calvillo S., Manning-Cela R.

Publicada: 1 ene 2013
Resumen:
To carry out the intracellular phase of its life cycle, Trypanosoma cruzi must infect a host cell. Although a few molecules have been reported to participate in this process, one known protein is LYT1, which promotes lysis under acidic conditions and is involved in parasite infection and development. Alternative transcripts from a single LYT1 gene generate two proteins with differential functions and compartmentalization. Single-gene products targeted to more than one location can interact with disparate proteins that might affect their function and targeting properties. The aim of this work was to study the LYT1 interaction map using coimmunoprecipitation assays with transgenic parasites expressing LYT1 products fused to GFP. We detected several proteins of sizes from 8 to 150 kDa that bind to LYT1 with different binding strengths. By MS-MS analysis, we identified proteins involved in parasite infectivity (trans-sialidase), development (kDSPs and histones H2A and H2B), and motility and protein traffic (dynein and a- and ß-tubulin), as well as protein-protein interactions (TPR-protein and kDSPs) and several hypothetical proteins. Our approach led us to identify the LYT1 interaction profile, thereby providing insights into the molecular mechanisms that contribute to parasite stage development and pathogenesis of T. cruzi infection. © 2013 C. Lugo-Caballero et al.

Filiaciones:
Lugo-Caballero C.:
 Departamento de Biomedicina Molecular, Centro de Investigación y Estudios Avanzados Del IPN, Avenida Instituto Politécnico Nacional No. 2508, 07360 Gustavo A. Madero, DF, Mexico

Ballesteros-Rodea G.:
 Departamento de Biomedicina Molecular, Centro de Investigación y Estudios Avanzados Del IPN, Avenida Instituto Politécnico Nacional No. 2508, 07360 Gustavo A. Madero, DF, Mexico

Martínez-Calvillo S.:
 Univ Nacl Autonoma Mexico, UBIMED, Fac Estudios Super Iztacala, Tlalnepantla 54090, Mex, Mexico

Manning-Cela R.:
 Departamento de Biomedicina Molecular, Centro de Investigación y Estudios Avanzados Del IPN, Avenida Instituto Politécnico Nacional No. 2508, 07360 Gustavo A. Madero, DF, Mexico
ISSN: 23146133
Editorial
HINDAWI PUBLISHING CORPORATION, 410 PARK AVENUE, 15TH FLOOR, #287 PMB, NEW YORK, NY 10022 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 2013 Número:
Páginas:
WOS Id: 000316895200001
ID de PubMed: 23586042
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