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-AP) 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 function. The success of this strategy suggests a general approach to discovering 'carbohydrate-active' partners in biology.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485602 | PMC |
http://dx.doi.org/10.1039/C3SC50826A | DOI Listing |
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