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Clathrin in Trypanosoma cruzi : In Silico Gene Identification, Isolation, and Localization of Protein Expression Sites
Author(s) -
CORRÊA JOSÉ R.,
ATELLA GEORGIA C.,
MENNABARRETO RUBEM S.,
SOARES MAURILIO J.
Publication year - 2007
Publication title -
journal of eukaryotic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 1066-5234
DOI - 10.1111/j.1550-7408.2007.00258.x
Subject(s) - clathrin , biology , clathrin adaptor proteins , microbiology and biotechnology , trypanosoma cruzi , golgi apparatus , endocytosis , population , signal transducing adaptor protein , biochemistry , signal transduction , receptor , endoplasmic reticulum , parasite hosting , world wide web , computer science , demography , sociology
. Clathrin is a scaffold protein found in different types of coated vesicles in most eukaryotic cells. Major forces that drive clathrin coat formation are the adaptor protein complexes. Trypanosoma cruzi is a flagellate protozoan that ingests macromolecules through receptor‐mediated endocytosis, but the molecules involved in this process are still poorly known. Bioinformatics was used to identify proteins in the T. cruzi genome database, permitting discrimination of the genes involved in clathrin coat assembly. Clathrin expression was demonstrated in T. cruzi epimastigotes by using several experimental approaches. Western blot analysis showed a single 180‐kDa protein band, which corresponds to the molecular mass of mammalian clathrin heavy chain. A flow cytometry assay demonstrated that the clathrin heavy chain was expressed in 97.74% of the cell population analyzed, with a high‐fluorescence signal. Immunofluorescence observation showed labeling clustered at the flagellar pocket and Golgi complex region. Coated vesicles budding off from the flagellar pocket and the trans Golgi network membranes were identified by transmission electron microscopy. Our data demonstrate the expression of clathrin in T. cruzi epimastigotes and show the association of this polypeptide with the parasite endocytic and exocytic pathways.