Abstract
Mono-ADP-ribosylation is a dynamic posttranslational modification (PTM) with important roles in signaling. Mammalian proteins that recognize or hydrolyze mono-ADP-ribosylated proteins have been described. We report the synthesis of ADP-ribosylated peptides from the proteins histone H2B, RhoA and, HNP-1. An innovative procedure was applied that makes use of pre-phosphorylated amino acid building blocks. Binding assays revealed that the macrodomains of human MacroD2 and TARG1 exhibit distinct specificities for the different ADP-ribosylated peptides, thus showing that the sequence surrounding ADP-ribosylated residues affects the substrate selectivity of macrodomains.
Keywords:
ADP-ribosylation; peptides; posttranslational modifications; proteins; solid-phase synthesis.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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ADP-Ribosylation*
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DNA Repair Enzymes / chemistry
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DNA Repair Enzymes / metabolism
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Histones / chemical synthesis*
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Histones / chemistry
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Histones / metabolism
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Humans
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Hydrolases / chemistry
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Hydrolases / metabolism
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Peptides / chemical synthesis*
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Peptides / chemistry
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Peptides / metabolism
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Protein Binding
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Protein Domains
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Solid-Phase Synthesis Techniques / methods*
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Thiolester Hydrolases / chemistry
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Thiolester Hydrolases / metabolism
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alpha-Defensins / chemical synthesis*
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alpha-Defensins / chemistry
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alpha-Defensins / metabolism
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rhoA GTP-Binding Protein / chemical synthesis*
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rhoA GTP-Binding Protein / chemistry
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rhoA GTP-Binding Protein / metabolism
Substances
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Histones
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MACROD2 protein, human
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Peptides
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alpha-Defensins
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human neutrophil peptide 1
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Hydrolases
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OARD1 protein, human
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Thiolester Hydrolases
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rhoA GTP-Binding Protein
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DNA Repair Enzymes