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TRYPANOSOMA CRUZI 229<br />

Mucins<br />

GIPLs<br />

LPPG<br />

Target sites for <strong>trans</strong>-sialylation reaction<br />

Mucins<br />

CO-EtN-PO 4<br />

2AEP<br />

Manα1,2Manα1,2Manα1,6Manα1,4GlcNα1,6-Inos-PO4-<br />

Alkylacylglycerol<br />

(epimastigotes/trypomastigotes)<br />

Ceramide<br />

(metacyclics)<br />

LPPG<br />

2AEP<br />

6<br />

Gal f β1,3Manα1,2Manα1,2Manα1,6Manα1,4-GlcNα1,6myo-Inos-PO 4 Ceramide<br />

Gal f β1,3<br />

FIGURE 10.2 Schematic representation of the surface coat of Trypanosoma cruzi. The cell surface of T. cruzi is<br />

covered with a dense layer of mucins, GIPLs (glycosylinositolphospholipids), and LPPG (lipopeptidophosphoglycan).<br />

The structures of the mucin anchors and the predominant LPPG species are outlined. AEP, aminoethylphosphonate;<br />

EtN, ethanolamine; GlcN, glucosamine; Inos, inositol.<br />

host glycoconjugates, thus accounting for<br />

the requirement for a <strong>trans</strong>-sialidase. The<br />

galactose-rich mucin is the acceptor for the<br />

<strong>trans</strong>-sialylation reaction in which 2,3-linked<br />

sialic acid residues are <strong>trans</strong>ferred from host<br />

glycoconjugates by the <strong>trans</strong>-sialidase enzyme<br />

to the terminal -galactose residues of the<br />

T. cruzi surface mucin. Interestingly, Endotrypanum,<br />

a trypanosomatid parasite of sloths,<br />

also has the ability to incorporate host-derived<br />

sialic acid into molecules on its own surface.<br />

The complete structures of the sialic acid<br />

acceptor O-linked oligosaccharide have been<br />

elucidated for epimastigotes of G strain and<br />

Y strain, and metacyclic forms of G strain. The<br />

structures of the O-linked oligosaccharides<br />

are conserved between the epimastigotes<br />

and the metacyclic trypomastigotes. However,<br />

BIOCHEMISTRY AND CELL BIOLOGY: PROTOZOA

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