Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar

Widescale evaluation of interacting partners for carbohydrates is an underexploited area. Probing of the 'glyco-interactome' has particular relevance given the lack of direct genetic control of glycoconjugate biosynthesis. Here we design, create and utilize a natural product-derived glycom...

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Main Authors: Cruz, I, Barry, C, Kramer, H, Chuang, C, Lloyd, S, van der Spoel, A, Platt, F, Yang, M, Davis, B
Format: Journal article
Language:English
Published: 2013
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author Cruz, I
Barry, C
Kramer, H
Chuang, C
Lloyd, S
van der Spoel, A
Platt, F
Yang, M
Davis, B
author_facet Cruz, I
Barry, C
Kramer, H
Chuang, C
Lloyd, S
van der Spoel, A
Platt, F
Yang, M
Davis, B
author_sort Cruz, I
collection OXFORD
description Widescale evaluation of interacting partners for carbohydrates is an underexploited area. Probing of the 'glyco-interactome' has particular relevance given the lack of direct genetic control of glycoconjugate biosynthesis. Here we design, create and utilize a natural product-derived glycomimetic iminosugar probe in a Glycomimetic Affinity-enrichment Proteomics (Glyco-AeP) strategy to elucidate key interactions directly from mammalian tissue. The binding partners discovered here and the associated genomic analysis implicate a subset of chaperone and junctional proteins as important in male fertility. Such repurposing of existing therapeutics thus creates direct routes to probing in vivo function. The success of this strategy suggests a general approach to discovering 'carbohydrate-active' partners in biology. © 2013 The Royal Society of Chemistry.
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spelling oxford-uuid:3ea367a1-6702-4f08-82d2-4e5bf3d2dce62022-03-26T14:26:44ZGlycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugarJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3ea367a1-6702-4f08-82d2-4e5bf3d2dce6EnglishSymplectic Elements at Oxford2013Cruz, IBarry, CKramer, HChuang, CLloyd, Svan der Spoel, APlatt, FYang, MDavis, BWidescale evaluation of interacting partners for carbohydrates is an underexploited area. Probing of the 'glyco-interactome' has particular relevance given the lack of direct genetic control of glycoconjugate biosynthesis. Here we design, create and utilize a natural product-derived glycomimetic iminosugar probe in a Glycomimetic Affinity-enrichment Proteomics (Glyco-AeP) strategy to elucidate key interactions directly from mammalian tissue. The binding partners discovered here and the associated genomic analysis implicate a subset of chaperone and junctional proteins as important in male fertility. Such repurposing of existing therapeutics thus creates direct routes to probing in vivo function. The success of this strategy suggests a general approach to discovering 'carbohydrate-active' partners in biology. © 2013 The Royal Society of Chemistry.
spellingShingle Cruz, I
Barry, C
Kramer, H
Chuang, C
Lloyd, S
van der Spoel, A
Platt, F
Yang, M
Davis, B
Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title_full Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title_fullStr Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title_full_unstemmed Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title_short Glycomimetic affinity-enrichment proteomics identifies partners for a clinically-utilized iminosugar
title_sort glycomimetic affinity enrichment proteomics identifies partners for a clinically utilized iminosugar
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