In‐Source Collision‐Induced Dissociation (CID) Improves Higher‐Energy Collisional Dissociation (HCD)‐Dependent Fragmentation of ADP‐Ribosyl Peptides

In-source CID converts ADP-ribosyl to phosphoribosyl-H<sub>2</sub>O peptides that are more amenable to HCD-dependent peptide sequencing, providing an alternative method for acceptor site determination when ETD-based methods are not available.

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Publication Details

Journal
Rapid Communications in Mass Spectrometry
Published
2024-12-04
DOI
https://doi.org/10.1002/rcm.9961
Citations
2
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
0.57

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article

In‐Source Collision‐Induced Dissociation (CID) Improves Higher‐Energy Collisional Dissociation (HCD)‐Dependent Fragmentation of ADP‐Ribosyl Peptides

Sasha A. Singh, Masanori Aikawa, Taku Kasai, Yuto Nakamura
2 citations
Rapid Communications in Mass Spectrometry
PARP inhibition in cancer therapy
0.57
article

In‐Source Collision‐Induced Dissociation (CID) Improves Higher‐Energy Collisional Dissociation (HCD)‐Dependent Fragmentation of ADP‐Ribosyl Peptides

Sasha A. Singh, Masanori Aikawa, Taku Kasai, Yuto Nakamura
article en
2 citations

Abstract

In-source CID converts ADP-ribosyl to phosphoribosyl-H<sub>2</sub>O peptides that are more amenable to HCD-dependent peptide sequencing, providing an alternative method for acceptor site determination when ETD-based methods are not available.

Rapid Communications in Mass SpectrometryVol. 39(4)
Brigham and Women's Hospital (US), Harvard University (US)
Kowa Company, National Heart, Lung, and Blood Institute
Affordable and clean energy
Openalex Percentile: Top 26%
PARP inhibition in cancer therapy
0.57
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