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Open AccessJournal ArticleDOI

What is the Sugar Code

TLDR
In this article, a large panel of sugar receptors (lectins) has developed based on more than a dozen fold changes in the glycan-lectin recognition process, and a large number of post-binding events.
Abstract
A code is defined by the nature of the symbols, which are used to generate information-storing combinations (e. g. oligo- and polymers). Like nucleic acids and proteins, oligo- and polysaccharides are ubiquitous, and they are a biochemical platform for establishing molecular messages. Of note, the letters of the sugar code system (third alphabet of life) excel in coding capacity by making an unsurpassed versatility for isomer (code word) formation possible by variability in anomery and linkage position of the glycosidic bond, ring size and branching. The enzymatic machinery for glycan biosynthesis (writers) realizes this enormous potential for building a large vocabulary. It includes possibilities for dynamic editing/erasing as known from nucleic acids and proteins. Matching the glycome diversity, a large panel of sugar receptors (lectins) has developed based on more than a dozen folds. Lectins 'read' the glycan-encoded information. Hydrogen/coordination bonding and ionic pairing together with stacking and C-H/π-interactions as well as modes of spatial glycan presentation underlie the selectivity and specificity of glycan-lectin recognition. Modular design of lectins together with glycan display and the nature of the cognate glycoconjugate account for the large number of post-binding events. They give an entry to the glycan vocabulary its functional, often context-dependent meaning(s), hereby building the dictionary of the sugar code.

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Citations
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Posted ContentDOI

A pore-forming β-trefoil lectin with specificity for the tumor-related glycosphingolipid Gb3

TL;DR: SaroL-1 from the lower eukaryote Salpingoeca rosetta was predicted to contain both β-trefoil and aerolysin-like pore-forming domain, with a stronger affinity for cancer-related α-galactosylated epitopes such as glycosphingolipid Gb3 embedded in giant unilamellar vesicles or cell membranes.
Journal ArticleDOI

Combination of High-Resolution Multistage Ion Mobility and Tandem MS with High Energy of Activation to Resolve the Structure of Complex Chemoenzymatically Synthesized Glycans.

TL;DR: The use of complementary strategies based on mass spectrometry to evaluate the ability of 14 engineered mutants of sucrose-utilizing α-transglucosylases to produce type/group-specific Shigella flexneri pentasaccharide bricks from a single lightly protected non-natural tetrasaccharides acceptor substrate illustrates the potential of the recently described powerful IMS and CTD-MS methods for the precise structural characterization of complex glycans.
Journal ArticleDOI

The choanoflagellate pore-forming lectin SaroL-1 punches holes in cancer cells by targeting the tumor-related glycosphingolipid Gb3

TL;DR: In this paper , a database of 44714 β-trefoil candidate lectins across 4497 species was searched for original domain combinations, which led to single out SaroL-1 in the choanoflagellate Salpingoeca rosetta.
Journal ArticleDOI

Multicomponent reaction derived small di- and tri-carbohydrate-based glycomimetics as tools for probing lectin specificity

TL;DR: A novel set of glycomimetic ligands through protection/deprotection multicomponent reactions (MCR) approach demonstrated different binding abilities for plant lectins Con A and UEA I, and human galectin-3.
References
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Translating the Histone Code

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Journal ArticleDOI

Dynamic RNA Modifications in Gene Expression Regulation

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