Molecular Tools for the Study of ADP-Ribosylation: A Unified and Versatile Method to Synthesise Native Mono-ADP-Ribosylated Peptides.

(ADP-ribosyl) hydrolase ADP-ribosylation poly(ADP-ribose) polymerases post-translational modification solid-phase peptide synthesis

Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
21 Jul 2021
Historique:
received: 28 01 2021
pubmed: 27 3 2021
medline: 24 7 2021
entrez: 26 3 2021
Statut: ppublish

Résumé

ADP-ribosylation (ADPr), as a post-translational modification, plays a crucial role in DNA-repair, immunity and many other cellular and physiological processes. Serine is the main acceptor for ADPr in DNA damage response, whereas the physiological impact of less common ADPr-modifications of cysteine and threonine side chains is less clear. Generally, gaining molecular insights into ADPr recognition and turn-over is hampered by the availability of homogeneous, ADP-ribosylated material, such as mono-ADP-ribosylated (MARylated) peptides. Here, a new and efficient solid-phase strategy for the synthesis of Ser-, Thr- and Cys-MARylated peptides is described. ADP-ribosylated cysteine, apart from being a native post-translational modification in its own right, proved to be suitable as a stabile bioisostere for ADP-ribosylated serine making it a useful tool to further biochemical research on serine ADP-ribosylation. In addition, it was discovered that the Streptococcus pyogenes encoded protein, SpyMacroD, acts as a Cys-(ADP-ribosyl) hydrolase.

Identifiants

pubmed: 33769608
doi: 10.1002/chem.202100337
pmc: PMC8360141
doi:

Substances chimiques

Peptides 0
Serine 452VLY9402

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10621-10627

Subventions

Organisme : Wellcome Trust
ID : 101794
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 210634
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R007195/1
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.

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Auteurs

Jim Voorneveld (J)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Johannes Gregor Matthias Rack (JGM)

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.

Luke van Gijlswijk (L)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Nico J Meeuwenoord (NJ)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Qiang Liu (Q)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Herman S Overkleeft (HS)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Gijsbert A van der Marel (GA)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

Ivan Ahel (I)

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.

Dmitri V Filippov (DV)

Leiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.

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