Literature DB >> 34816463

Assay technologies facilitating drug discovery for ADP-ribosyl writers, readers and erasers.

Tuomo Glumoff1, Sven T Sowa1, Lari Lehtiö1.   

Abstract

ADP-ribosylation is a post-translational modification catalyzed by writer enzymes - ADP-ribosyltransferases. The modification is part of many signaling events, can modulate the function and stability of target proteins, and often results in the recruitment of reader proteins that bind to the ADP-ribosyl groups. Erasers are integral actors in these signaling events and reverse the modification. ADP-ribosylation can be targeted with therapeutics and many inhibitors against writers exist, with some being in clinical use. Inhibitors against readers and erasers are sparser and development of these has gained momentum only in recent years. Drug discovery has been hampered by the lack of specific tools, however many significant advances in the methods have recently been reported. We discuss assays used in the field with a focus on methods allowing efficient identification of small molecule inhibitors and profiling against enzyme families. While human proteins are focused, the methods can be also applied to bacterial toxins and virus encoded erasers that can be targeted to treat infectious diseases in the future.
© 2021 Wiley Periodicals LLC.

Entities:  

Keywords:  ADP-ribosylation; ADP-ribosylhydrolase; ADP-ribosyltransferase; drug discovery; high-throughput assay; post-translational modification

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Year:  2021        PMID: 34816463     DOI: 10.1002/bies.202100240

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  3 in total

1.  Protein engineering approach to enhance activity assays of mono-ADP-ribosyltransferases through proximity.

Authors:  Albert Galera-Prat; Juho Alaviuhkola; Heli I Alanen; Lari Lehtiö
Journal:  Protein Eng Des Sel       Date:  2022-02-17       Impact factor: 1.952

Review 2.  Medicinal Chemistry Perspective on Targeting Mono-ADP-Ribosylating PARPs with Small Molecules.

Authors:  Maria Giulia Nizi; Mirko M Maksimainen; Lari Lehtiö; Oriana Tabarrini
Journal:  J Med Chem       Date:  2022-05-24       Impact factor: 8.039

3.  Design, synthesis and evaluation of inhibitors of the SARS-CoV-2 nsp3 macrodomain.

Authors:  Lavinia M Sherrill; Elva E Joya; AnnMarie Walker; Anuradha Roy; Yousef M Alhammad; Moriama Atobatele; Sarah Wazir; George Abbas; Patrick Keane; Junlin Zhuo; Anthony K L Leung; David K Johnson; Lari Lehtiö; Anthony R Fehr; Dana Ferraris
Journal:  Bioorg Med Chem       Date:  2022-05-11       Impact factor: 3.461

  3 in total

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