Literature DB >> 20672277

Glycosyltransferases and their assays.

Gerd K Wagner1, Thomas Pesnot.   

Abstract

Glycosyltransferases (GTs) are a large family of enzymes that are essential in all domains of life for the biosynthesis of complex carbohydrates and glycoconjugates. GTs catalyse the transfer of a sugar from a glycosyl donor to a variety of acceptor molecules, for example, oligosaccharides, peptides, lipids or small molecules. Such glycosylation reactions are central to many fundamental biological processes, including cellular adhesion, cell signalling and bacterial- and plant-cell-wall biosynthesis. GTs are therefore of significant interest as molecular targets in chemical biology and drug discovery. In addition, GTs have found wide application as synthetic tools for the preparation of complex carbohydrates and glycoconjugates. In order to exploit the potential of GTs both as molecular targets and synthetic tools, robust and operationally simple bioassays are essential, especially as more and more protein sequences with putative GT activity but unknown biochemical function are being identified. In this minireview, we give a brief introduction to GT biochemistry and biology. We outline the relevance of GTs for medicinal chemistry and chemical biology, and describe selected examples for recently developed GT bioassays, with a particular emphasis on fluorescence-based formats.

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Year:  2010        PMID: 20672277     DOI: 10.1002/cbic.201000201

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  22 in total

Review 1.  The structural biology of enzymes involved in natural product glycosylation.

Authors:  Shanteri Singh; George N Phillips; Jon S Thorson
Journal:  Nat Prod Rep       Date:  2012-06-12       Impact factor: 13.423

2.  New α-glucosides of caffeoyl quinic acid from the leaves of Moringa oleifera Lam.

Authors:  Yoshiki Kashiwada; Fakhruddin Ali Ahmed; Shin-ichiro Kurimoto; Sang-Yong Kim; Hirofumi Shibata; Toshihiro Fujioka; Yoshihisa Takaishi
Journal:  J Nat Med       Date:  2011-07-05       Impact factor: 2.343

3.  Development of a universal glycosyltransferase assay amenable to high-throughput formats.

Authors:  Hyun Soo Lee; Jon S Thorson
Journal:  Anal Biochem       Date:  2011-07-08       Impact factor: 3.365

4.  Distinct Substrate Specificity and Catalytic Activity of the Pseudoglycosyltransferase VldE.

Authors:  Hatem A Abuelizz; Taifo Mahmud
Journal:  Chem Biol       Date:  2015-06-04

5.  Rapid screening of sugar-nucleotide donor specificities of putative glycosyltransferases.

Authors:  M Osman Sheikh; Stephanie M Halmo; Sneha Patel; Dustin Middleton; Hideyuki Takeuchi; Christopher M Schafer; Christopher M West; Robert S Haltiwanger; Fikri Y Avci; Kelley W Moremen; Lance Wells
Journal:  Glycobiology       Date:  2017-03-01       Impact factor: 4.313

6.  Structural and biochemical analysis of a bacterial glycosyltransferase.

Authors:  Fan Zhu; Ren Wu; Hua Zhang; Hui Wu
Journal:  Methods Mol Biol       Date:  2013

7.  Identification of non-substrate-like glycosyltransferase inhibitors from library screening: pitfalls & hits.

Authors:  Masaki Ema; Yong Xu; Sebastian Gehrke; Gerd K Wagner
Journal:  Medchemcomm       Date:  2017-11-29       Impact factor: 3.597

8.  Using simple donors to drive the equilibria of glycosyltransferase-catalyzed reactions.

Authors:  Richard W Gantt; Pauline Peltier-Pain; William J Cournoyer; Jon S Thorson
Journal:  Nat Chem Biol       Date:  2011-08-21       Impact factor: 15.040

9.  Novel insights into the diversity of catabolic metabolism from ten haloarchaeal genomes.

Authors:  Iain Anderson; Carmen Scheuner; Markus Göker; Kostas Mavromatis; Sean D Hooper; Iris Porat; Hans-Peter Klenk; Natalia Ivanova; Nikos Kyrpides
Journal:  PLoS One       Date:  2011-05-25       Impact factor: 3.240

10.  A neutral diphosphate mimic crosslinks the active site of human O-GlcNAc transferase.

Authors:  Jiaoyang Jiang; Michael B Lazarus; Lincoln Pasquina; Piotr Sliz; Suzanne Walker
Journal:  Nat Chem Biol       Date:  2011-11-13       Impact factor: 15.040

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