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. Author manuscript; available in PMC: 2019 Jan 30.
Published in final edited form as: Biochemistry. 2018 Jan 19;57(4):429–440. doi: 10.1021/acs.biochem.7b01022

Table 2.

Summary of the different MS methodologies for the analysis of the ADP-ribosylated proteome. (site) indicates the studies where ADP-ribosylation site information is obtained. CID, collision-induced dissociation; HCD, higher-energy collisional dissociation; ETD, electron transfer dissociation; ETcaD, electron-transfer dissociation with supplemental collisional activation; EThcD, electron-transfer/higher-energy collision dissociation.

Affinity purification Binding Specificity Fragmentation MS2 Reference
Af1521 macrodomain Bind to both mono- and poly-ADP-ribose CID Dani et al., 2009
Af1521 macrodomain Bind to both mono- and poly-ADP-ribose HCD Jungmichel et al., 2009
10H antibody Bind to poly-ADP-ribose (only units >10) CID Gagné et al., 2008
PARG-DEAD (catalytically inactive PARG) Bind to poly-ADP-ribose CID Gagné et al., 2012
IMAC For phosphopeptide enrichment CID (site) Chapman et al., 2013
IMAC For phosphopeptide enrichment CID/HCD (site) Daniels et al., 2014
Boronate affinity chromatography Boron forms ester bonds with the 1,2-cis-diol moiety in ADP-ribose; Asp-/Glu-ADP-ribose converted to hydroxamic acid CID (site) Zhang et al., 2013
IMAC For phosphopeptide enrichment ETD (site) Leidecker et al., 2016
Af1521 macrodomain Bind to both mono- and poly-ADP-ribose HCD/ETD (site) Martello et al., 2016
Af1521 macrodomain Bind to both mono- and poly-ADP-ribose HCD/ETcaD/EThcD (site) Bilan et al., 2017