<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Balouz V</submitter><funding>CONICET</funding><funding>Agencia Nacional de PromociÃ³n CientÃfica y TecnolÃ³gica</funding><pagination>e0013728</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12915924</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Chagas disease (ChD), caused by the parasitic protozoan Trypanosoma cruzi, is a lifelong, neglected tropical disease with substantial medical and socioeconomic impact. Despite this situation, currently available diagnostic and therapeutic methods display serious limitations. A promising strategy to improve ChD serodiagnosis involves targeting parasite carbohydrate antigens, particularly the α-galactosyl-rich mucins that coat the surface of bloodstream trypomastigotes (tGPI-mucins).&lt;h4>Methods/principle findings&lt;/h4>Here, we present a concise and efficient protocol for the chemical synthesis of a tGPI-mucin-derived glycotope, the disaccharide α-D-Galp-(1 → 3)-β-D-Galp, and its functional conjugation to different scaffolds using the squarate method. A neoglycoprotein made </pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pubmed_title>Conjugates of α-d-Galp-(1→3)-β-d-Galp for the serological diagnosis of Chagas disease.</pubmed_title><pmcid>PMC12915924</pmcid><funding_grant_id>PICT-2021-I-A-00284</funding_grant_id><funding_grant_id>PICT-2021-I-A-00441</funding_grant_id><pubmed_authors>Melli LJ</pubmed_authors><pubmed_authors>Altcheh J</pubmed_authors><pubmed_authors>Ducrey I</pubmed_authors><pubmed_authors>Abal M</pubmed_authors><pubmed_authors>Balouz V</pubmed_authors><pubmed_authors>Marino C</pubmed_authors><pubmed_authors>Lopez R</pubmed_authors><pubmed_authors>Buscaglia CA</pubmed_authors><pubmed_authors>de Lederkremer RM</pubmed_authors><pubmed_authors>Ciocchini AE</pubmed_authors><pubmed_authors>Conte N</pubmed_authors><pubmed_authors>Giorgi ME</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conjugates of α-d-Galp-(1→3)-β-d-Galp for the serological diagnosis of Chagas disease.</name><description>&lt;h4>Background&lt;/h4>Chagas disease (ChD), caused by the parasitic protozoan Trypanosoma cruzi, is a lifelong, neglected tropical disease with substantial medical and socioeconomic impact. Despite this situation, currently available diagnostic and therapeutic methods display serious limitations. A promising strategy to improve ChD serodiagnosis involves targeting parasite carbohydrate antigens, particularly the α-galactosyl-rich mucins that coat the surface of bloodstream trypomastigotes (tGPI-mucins).&lt;h4>Methods/principle findings&lt;/h4>Here, we present a concise and efficient protocol for the chemical synthesis of a tGPI-mucin-derived glycotope, the disaccharide α-D-Galp-(1 → 3)-β-D-Galp, and its functional conjugation to different scaffolds using the squarate method. A neoglycoprotein made </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-09T11:05:15.708Z</modification><creation>2026-07-09T10:41:05.988Z</creation></dates><accession>S-EPMC12915924</accession><cross_references><pubmed>41666228</pubmed><doi>10.1371/journal.pntd.0013728</doi></cross_references></HashMap>