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Metabolic Labeling of Surface Neo-sialylglyconjugates Catalyzed by Trypanosoma cruzi trans-Sialidase

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Part of the book series: Methods in Molecular Biology ((MIMB,volume 1955))

Abstract

Trypanosoma cruzi, the protozoan agent of Chagas disease, has evolved an innovative metabolic pathway by which protective sialic acid (SA) residues are scavenged from host sialylglycoconjugates and transferred onto parasite surface mucin-like molecules (or surface glycoconjugates from host target cells) by means of a unique trans-sialidase (TS) enzyme. TS-induced changes in the glycoprotein sialylation profile of both parasite and host cells are crucial for the establishment of a persistent T. cruzi infection and for the development of Chagas disease-associated pathogenesis. In this chapter, we describe a novel metabolic labeling method developed in our labs that enables straightforward identification and molecular characterization of SA acceptors of the TS-catalyzed reaction.

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Acknowledgments

GC and MS hold fellowships from CONICET, and MdlMC, CAB, OC and JM are career investigators from the same Institution. This work was supported by the National Institute of Health R01AI104531 to OC, and Agencia Nacional de Promoción Científica y Tecnológica PICT2012-1815 to JM. The funders had no role in decision to publish or preparation of the manuscript.

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Correspondence to Juan Mucci .

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Carlevaro, G. et al. (2019). Metabolic Labeling of Surface Neo-sialylglyconjugates Catalyzed by Trypanosoma cruzi trans-Sialidase. In: Gómez, K., Buscaglia, C. (eds) T. cruzi Infection. Methods in Molecular Biology, vol 1955. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-9148-8_10

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  • DOI: https://doi.org/10.1007/978-1-4939-9148-8_10

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