Literature DB >> 33729259

Development of a 1,2-difluorofucoside activity-based probe for profiling GH29 fucosidases.

Yvette M C A Luijkx1, Seino Jongkees, Karin Strijbis, Tom Wennekes.   

Abstract

GH29 α-l-fucosidases catalyze hydrolysis of terminal α-l-fucosyl linkages with varying specificity and are expressed by prominent members of the human gut microbiota. Both homeostasis and dysbiosis at the human intestinal microbiota interface have been correlated with altered fucosidase activity. Herein we describe the development of a 2-deoxy-2-fluoro fucosyl fluoride derivative with an azide mini-tag as an activity-based probe (ABP) for selective in vitro labelling of GH29 α-l-fucosidases. Only catalytically active fucosidases are inactivated by this ABP, allowing their functionalization with a biotin reporter group via the CuAAC reaction and subsequent in-gel detection at nanogram levels. The ABP we present here is shown to be active against a GH29 α-l-fucosidase from Bacteroides fragilis and capable of labeling two other GH29 α-l-fucosidases with different linkage specificity, illustrating its broader utility. This novel ABP is a valuable addition to the toolbox of fucosidase probes by allowing identification and functional studies of the wide variety of GH29 fucosidases, including those in the gut microbiota.

Entities:  

Year:  2021        PMID: 33729259     DOI: 10.1039/d1ob00054c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Azido Groups Hamper Glycan Acceptance by Carbohydrate Processing Enzymes.

Authors:  Feng Liu; Hong-Ming Chen; Zachary Armstrong; Stephen G Withers
Journal:  ACS Cent Sci       Date:  2022-05-10       Impact factor: 18.728

Review 2.  Sweet impersonators: Molecular mimicry of host glycans by bacteria.

Authors:  Hanna de Jong; Marc M S M Wösten; Tom Wennekes
Journal:  Glycobiology       Date:  2022-02-26       Impact factor: 4.313

  2 in total

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