Literature DB >> 33434850

O-GlcNAcylated peptides and proteins for structural and functional studies.

Aaron T Balana1, Stuart P Moon1, Matthew R Pratt2.   

Abstract

O-GlcNAcylation is an enzymatic post-translational modification occurring in hundreds of protein substrates. This modification occurs through the addition of the monosaccharide N-acetylglucosamine to serine and threonine residues on intracellular proteins in the cytosol, nucleus, and mitochondria. As a highly dynamic form of modification, changes in O-GlcNAc levels coincide with alterations in metabolic state, the presence of stressors, and cellular health. At the protein level, the consequences of the sugar modification can vary, thus necessitating biochemical investigations on protein-specific and site-specific effects. To this end, enzymatic and chemical methods to 'encode' the modification have been developed and the utilization of these synthetic glycopeptides and glycoproteins has since been instrumental in the discovery of the mechanisms by which O-GlcNAcylation can affect a diverse array of biological processes.
Copyright © 2020 Elsevier Ltd. All rights reserved.

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Year:  2021        PMID: 33434850      PMCID: PMC8222092          DOI: 10.1016/j.sbi.2020.12.005

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   7.786


  69 in total

1.  A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo.

Authors:  Scott A Yuzwa; Matthew S Macauley; Julia E Heinonen; Xiaoyang Shan; Rebecca J Dennis; Yuan He; Garrett E Whitworth; Keith A Stubbs; Ernest J McEachern; Gideon J Davies; David J Vocadlo
Journal:  Nat Chem Biol       Date:  2008-06-29       Impact factor: 15.040

2.  The New Chemical Reporter 6-Alkynyl-6-deoxy-GlcNAc Reveals O-GlcNAc Modification of the Apoptotic Caspases That Can Block the Cleavage/Activation of Caspase-8.

Authors:  Kelly N Chuh; Anna R Batt; Balyn W Zaro; Narek Darabedian; Nicholas P Marotta; Caroline K Brennan; Arya Amirhekmat; Matthew R Pratt
Journal:  J Am Chem Soc       Date:  2017-05-31       Impact factor: 15.419

3.  Posttranslational mutagenesis: A chemical strategy for exploring protein side-chain diversity.

Authors:  Tom H Wright; Ben J Bower; Justin M Chalker; Gonçalo J L Bernardes; Rafal Wiewiora; Wai-Lung Ng; Ritu Raj; Sarah Faulkner; M Robert J Vallée; Anuchit Phanumartwiwath; Oliver D Coleman; Marie-Laëtitia Thézénas; Maola Khan; Sébastien R G Galan; Lukas Lercher; Matthew W Schombs; Stefanie Gerstberger; Maria E Palm-Espling; Andrew J Baldwin; Benedikt M Kessler; Timothy D W Claridge; Shabaz Mohammed; Benjamin G Davis
Journal:  Science       Date:  2016-09-22       Impact factor: 47.728

4.  Structures of human O-GlcNAcase and its complexes reveal a new substrate recognition mode.

Authors:  Baobin Li; Hao Li; Lei Lu; Jiaoyang Jiang
Journal:  Nat Struct Mol Biol       Date:  2017-03-20       Impact factor: 15.369

5.  O-GlcNAc modification inhibits the calpain-mediated cleavage of α-synuclein.

Authors:  Paul M Levine; Cesar A De Leon; Ana Galesic; Aaron Balana; Nicholas P Marotta; Yuka E Lewis; Matthew R Pratt
Journal:  Bioorg Med Chem       Date:  2017-04-29       Impact factor: 3.641

6.  α-Synuclein O-GlcNAcylation alters aggregation and toxicity, revealing certain residues as potential inhibitors of Parkinson's disease.

Authors:  Paul M Levine; Ana Galesic; Aaron T Balana; Anne-Laure Mahul-Mellier; Mariana X Navarro; Cesar A De Leon; Hilal A Lashuel; Matthew R Pratt
Journal:  Proc Natl Acad Sci U S A       Date:  2019-01-16       Impact factor: 11.205

7.  Glycopeptide-specific monoclonal antibodies suggest new roles for O-GlcNAc.

Authors:  Chin Fen Teo; Sampat Ingale; Margreet A Wolfert; Galal A Elsayed; Laszlo G Nöt; John C Chatham; Lance Wells; Geert-Jan Boons
Journal:  Nat Chem Biol       Date:  2010-03-21       Impact factor: 15.040

8.  Structural insights into the substrate binding adaptability and specificity of human O-GlcNAcase.

Authors:  Baobin Li; Hao Li; Chia-Wei Hu; Jiaoyang Jiang
Journal:  Nat Commun       Date:  2017-09-22       Impact factor: 14.919

9.  Generation of a synthetic GlcNAcylated nucleosome reveals regulation of stability by H2A-Thr101 GlcNAcylation.

Authors:  Lukas Lercher; Ritu Raj; Nisha A Patel; Joshua Price; Shabaz Mohammed; Carol V Robinson; Christopher J Schofield; Benjamin G Davis
Journal:  Nat Commun       Date:  2015-08-25       Impact factor: 14.919

10.  Thio-Linked UDP-Peptide Conjugates as O-GlcNAc Transferase Inhibitors.

Authors:  Karim Rafie; Andrii Gorelik; Riccardo Trapannone; Vladimir S Borodkin; Daan M F van Aalten
Journal:  Bioconjug Chem       Date:  2018-05-10       Impact factor: 4.774

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  1 in total

1.  O-GlcNAcylation of High Mobility Group Box 1 (HMGB1) Alters Its DNA Binding and DNA Damage Processing Activities.

Authors:  Aaron T Balana; Anirban Mukherjee; Harsh Nagpal; Stuart P Moon; Beat Fierz; Karen M Vasquez; Matthew R Pratt
Journal:  J Am Chem Soc       Date:  2021-09-21       Impact factor: 16.383

  1 in total

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