IMIBIO-SL   20937
INSTITUTO MULTIDISCIPLINARIO DE INVESTIGACIONES BIOLOGICAS DE SAN LUIS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
STRUCTURAL BIOLOGY OF T. cruzi mRNA MADURATION PROTEINS AS POTENTIAL TARGET FOR DRUG DESING
Autor/es:
CARMONA N, GÓMEZ BARROSO JA, BERCOVICH N, VAZQUEZ M, AGUILAR CF.
Lugar:
Mendoza
Reunión:
Congreso; XXVI Annual Scientific Meeting of Cuyo Biology Society; 2008
Institución organizadora:
Sociedad de Biología de Cuyo
Resumen:
STRUCTURAL BIOLOGY OF T. cruzi mRNA MADURATION
PROTEINS AS POTENTIAL TARGET FOR DRUG DESING
Carmona N, Gómez Barroso JA, Bercovich N, Vazquez M,
Aguilar CF.
Lab de Biol Mol Estructural, Univ. Nac de San Luis, San Lui 5700.
E-mail: natycarmona04@hotmail.com
Trypanosoma cruzi is the etiologic agent of Chagas disease. The
objective of our work is the resolution by X-ray crystallography o
the three-dimensional structure of T. cruzi proteins involved in
mRNA cleavage and polyadenylation as a first step for rationa drug
design. The main objective of the Chagas´ Disease Research Network
is the search for protein targets in metabolic routes absen in
the human host and common in trypanosomatids. The T. cruz proteins
studied in this work are: TcFIP1-like (factor interacting with
Pap1) and TcCPSF30 (cleavaje and polyadenylation facto 30). They
were expressed in E. coli as fusion proteins with N terminal Histag.
We have overexpressed and purified them Refolding assays
were realized for TcCPSF30. The refolded protein was used for
crystallization and other structural studies TcFIP1-like was
overexpressed in soluble form and was purifided Different
bioinformatic studies showed structural particularitie with a high
potential for drug design.