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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 |
Appears in Collections: | Staff Publications Elements |
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