Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0162528
Title: An alternative strategy for pan-acetyl-lysine antibody generation
Authors: Kim S.-Y.
Sim C.K.
Zhang Q.
Tang H.
Brunmeir R. 
Pan H.
Karnani N.
Han W. 
Zhang K.
Xu F. 
Keywords: pan acetyl lysine antibody
protein antibody
unclassified drug
antibody
lysine
peptide
amino acid sequence
animal experiment
antibody specificity
antigen binding
antigen recognition
Article
cellular distribution
controlled study
dot hybridization
enzyme linked immunosorbent assay
immunoreactivity
male
New Zealand White (rabbit)
nonhuman
protein acetylation
protein determination
sequence analysis
validation process
3T3-L1 cell line
acetylation
animal
chemistry
consensus sequence
gene ontology
HEK293 cell line
human
immunoassay
liquid chromatography
metabolism
metabolome
mouse
protein motif
rabbits and hares
reproducibility
tandem mass spectrometry
3T3-L1 Cells
Acetylation
Amino Acid Motifs
Animals
Antibodies
Chromatography, Liquid
Consensus Sequence
Enzyme-Linked Immunosorbent Assay
Gene Ontology
HEK293 Cells
Humans
Immunoassay
Lysine
Male
Metabolome
Mice
Peptides
Rabbits
Reproducibility of Results
Tandem Mass Spectrometry
Issue Date: 2016
Citation: Kim S.-Y., Sim C.K., Zhang Q., Tang H., Brunmeir R., Pan H., Karnani N., Han W., Zhang K., Xu F. (2016). An alternative strategy for pan-acetyl-lysine antibody generation. PLoS ONE 11 (9) : e0162528. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0162528
Rights: Attribution 4.0 International
Abstract: Lysine acetylation is an important post-translational modification in cell signaling. In acetylome studies, a high-quality pan-acetyl-lysine antibody is key to successful enrichment of acetylated peptides for subsequent mass spectrometry analysis. Here we show an alternative method to generate polyclonal pan-acetyl-lysine antibodies using a synthesized random library of acetylated peptides as the antigen. Our antibodies are tested to be specific for acetyl-lysine peptides/proteins via ELISA and dot blot. When pooled, five of our antibodies show broad reactivity to acetyl-lysine peptides, complementing a commercial antibody in terms of peptide coverage. The consensus sequence of peptides bound by our antibody cocktail differs slightly from that of the commercial antibody. Lastly, our antibodies are tested in a proof-of-concept to analyze the acetylome of HEK293 cells. In total we identified 1557 acetylated peptides from 416 proteins. We thus demonstrated that our antibodies are well-qualified for acetylome studies and can complement existing commercial antibodies. © 2016 Kim et al.This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161554
ISSN: 19326203
DOI: 10.1371/journal.pone.0162528
Rights: Attribution 4.0 International
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