Quantification of N 6 ‐formylated lysine in bacterial protein digests using liquid chromatography/tandem mass spectrometry despite spontaneous formation and matrix effects-Reference-Cited by-同舟云学术

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Quantification of N 6 ‐formylated lysine in bacterial protein digests using liquid chromatography/tandem mass spectrometry despite spontaneous formation and matrix effects

Published:2021-01-20 Issue:5 Volume:35 Page:
ISSN:0951-4198
Container-title:Rapid Communications in Mass Spectrometry
language:en
Short-container-title:Rapid Commun Mass Spectrom

Author:

Folz Jacob S.¹^ORCID,Patterson Jenelle A.²,Hanson Andrew D.²,Fiehn Oliver¹^ORCID

Affiliation:

1. West Coast Metabolomics Center University of California Davis Davis CA USA

2. Horticultural Sciences Department University of Florida Gainesville Gainesville FL USA

Funder

National Science Foundation

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rcm.9019

Reference18 articles.

1. Lysine Acetylation Goes Global: From Epigenetics to Metabolism and Therapeutics

2. N ε -Formylation of lysine is a widespread post-translational modification of nuclear proteins occurring at residues involved in regulation of chromatin function

3. Dissolving Peptides in 0.1% Formic Acid Brings Risk of Artificial Formylation

4. Dosimetry of N6-Formyllysine Adducts Following [13C2H2]-Formaldehyde Exposures in Rats

5. Quantitation of N6-Formyl-lysine Adduct Following Aristolochic Acid Exposure in Cells and Rat Tissues by Liquid Chromatography-Tandem Mass Spectrometry Coupled with Stable Isotope-Dilution Method

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