Galactose Recognition by the Apicomplexan Parasite Toxoplasma gondii


Autoria(s): Marchant, Jan; Cowper, Ben; Liu, Yan; Lai, Livia; Pinzan, Camila; Marq, Jean Baptiste; Friedrich, Nikolas; Sawmynaden, Kovilen; Liew, Lloyd; Chai, Wengang; Childs, Robert A.; Saouros, Savvas; Simpson, Peter; Roque Barreira, Maria Cristina; Feizi, Ten; Soldati-Favre, Dominique; Matthews, Stephen
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

Toxosplasma gondii is the model parasite of the phylum Apicomplexa, which contains numerous obligate intracellular parasites of medical and veterinary importance, including Eimeria, Sarcocystis, Cryptosporidium, Cyclospora, and Plasmodium species. Members of this phylum actively enter host cells by a multistep process with the help of microneme protein (MIC) complexes that play important roles in motility, host cell attachment, moving junction formation, and invasion. T. gondii (Tg)MIC1-4-6 complex is the most extensively investigated microneme complex, which contributes to host cell recognition and attachment via the action of TgMIC1, a sialic acid-binding adhesin. Here, we report the structure of TgMIC4 and reveal its carbohydrate-binding specificity to a variety of galactose-containing carbohydrate ligands. The lectin is composed of six apple domains in which the fifth domain displays a potent galactose-binding activity, and which is cleaved from the complex during parasite invasion. We propose that galactose recognition by TgMIC4 may compromise host protection from galectin-mediated activation of the host immune system.

Medical Research Council [G0800038, G9601454]

Medical Research Council

Swiss National Foundation UK Research Councils Basic Technology Initiative

Swiss National Foundation UK Research Councils' Basic Technology Initiative

EPSRC

EPSRC [GRS/79268, EP/G037604/1]

European Union

European Union

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, BETHESDA, v. 287, n. 20, supl. 1, Part 1, pp. 16720-16733, MAY 11, 2012

0021-9258

http://www.producao.usp.br/handle/BDPI/41930

10.1074/jbc.M111.325928

http://dx.doi.org/10.1074/jbc.M111.325928

Idioma(s)

eng

Publicador

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

BETHESDA

Relação

JOURNAL OF BIOLOGICAL CHEMISTRY

Direitos

closedAccess

Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Palavras-Chave #HOST-CELL INVASION #NEOSPORA-CANINUM #MICRONEMAL PROTEINS #CRYSTAL-STRUCTURES #PLASMA-MEMBRANE #GM1 GANGLIOSIDE #BINDING LECTIN #APPLE DOMAINS #IDENTIFICATION #OLIGOSACCHARIDE #BIOCHEMISTRY & MOLECULAR BIOLOGY
Tipo

article

original article

publishedVersion