Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0162528
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dc.titleAn alternative strategy for pan-acetyl-lysine antibody generation
dc.contributor.authorKim S.-Y.
dc.contributor.authorSim C.K.
dc.contributor.authorZhang Q.
dc.contributor.authorTang H.
dc.contributor.authorBrunmeir R.
dc.contributor.authorPan H.
dc.contributor.authorKarnani N.
dc.contributor.authorHan W.
dc.contributor.authorZhang K.
dc.contributor.authorXu F.
dc.date.accessioned2019-11-06T07:46:31Z
dc.date.available2019-11-06T07:46:31Z
dc.date.issued2016
dc.identifier.citationKim 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
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161554
dc.description.abstractLysine 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectpan acetyl lysine antibody
dc.subjectprotein antibody
dc.subjectunclassified drug
dc.subjectantibody
dc.subjectlysine
dc.subjectpeptide
dc.subjectamino acid sequence
dc.subjectanimal experiment
dc.subjectantibody specificity
dc.subjectantigen binding
dc.subjectantigen recognition
dc.subjectArticle
dc.subjectcellular distribution
dc.subjectcontrolled study
dc.subjectdot hybridization
dc.subjectenzyme linked immunosorbent assay
dc.subjectimmunoreactivity
dc.subjectmale
dc.subjectNew Zealand White (rabbit)
dc.subjectnonhuman
dc.subjectprotein acetylation
dc.subjectprotein determination
dc.subjectsequence analysis
dc.subjectvalidation process
dc.subject3T3-L1 cell line
dc.subjectacetylation
dc.subjectanimal
dc.subjectchemistry
dc.subjectconsensus sequence
dc.subjectgene ontology
dc.subjectHEK293 cell line
dc.subjecthuman
dc.subjectimmunoassay
dc.subjectliquid chromatography
dc.subjectmetabolism
dc.subjectmetabolome
dc.subjectmouse
dc.subjectprotein motif
dc.subjectrabbits and hares
dc.subjectreproducibility
dc.subjecttandem mass spectrometry
dc.subject3T3-L1 Cells
dc.subjectAcetylation
dc.subjectAmino Acid Motifs
dc.subjectAnimals
dc.subjectAntibodies
dc.subjectChromatography, Liquid
dc.subjectConsensus Sequence
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectGene Ontology
dc.subjectHEK293 Cells
dc.subjectHumans
dc.subjectImmunoassay
dc.subjectLysine
dc.subjectMale
dc.subjectMetabolome
dc.subjectMice
dc.subjectPeptides
dc.subjectRabbits
dc.subjectReproducibility of Results
dc.subjectTandem Mass Spectrometry
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1371/journal.pone.0162528
dc.description.sourcetitlePLoS ONE
dc.description.volume11
dc.description.issue9
dc.description.pagee0162528
dc.published.statePublished
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