Evidence map›Paper›PMID 33769608›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2021

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

Jim Voorneveld, Johannes Gregor Matthias Rack, Luke van Gijlswijk, Nico J Meeuwenoord, Qiang Liu, Herman S Overkleeft, Gijsbert A van der Marel, Ivan Ahel, Dmitri V Filippov

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Solid-Phase Synthesis and Biological Evaluation of Peptides ADP-Ribosylated at Histidine.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Jim VoorneveldLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Johannes Gregor Matthias RackSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.
Luke van GijlswijkLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Nico J MeeuwenoordLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Qiang LiuLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Herman S OverkleeftLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Gijsbert A van der MarelLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.
Ivan AhelSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.
Dmitri V FilippovLeiden Institute of Chemistry, Leiden University, Department of Bioorganic Synthesis, Einsteinweg 55, 2333CC, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-6978-7425
Leiden University · NLUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R007195/1Cancer Research UK 22284Wellcome Trust 101794Wellcome Trust 210634Wellcome Trust 210634/Z/18/Z
6 · The paper itself

Abstract

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.

Indexed as

ADP-RibosylationSerineDNA RepairPeptidesProtein Processing, Post-TranslationalPeptidesSerineADP-ribosylation(ADP-ribosyl) hydrolasepoly(ADP-ribose) polymerasespost-translational modificationsolid-phase peptide synthesis

Identifiers

PMID33769608
PMCPMC8360141
OpenAlexW3137549295

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.