Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
31
pubmed:dateCreated
2004-7-26
pubmed:abstractText
14-3-3 proteins regulate the cell division cycle and play a pivotal role in blocking cell cycle advancement after activation of the DNA replication and DNA damage checkpoints. Here we describe a global proteomics analysis to identify proteins that bind to 14-3-3s during interphase and mitosis. 14-3-3-binding proteins were purified from extracts of interphase and mitotic HeLa cells using specific peptide elution from 14-3-3 zeta affinity columns. Proteins that specifically bound and eluted from the affinity columns were identified by microcapillary high pressure liquid chromatography tandem mass spectrometry analysis. Several known and novel 14-3-3-interacting proteins were identified in this screen. Identified proteins are involved in cell cycle regulation, signaling, metabolism, protein synthesis, nucleic acid binding, chromatin structure, protein folding, proteolysis, nucleolar function, and nuclear transport as well as several other cellular processes. In some cases 14-3-3 binding was cell cycle-dependent, whereas in other cases the binding was shown to be cell cycle-independent. This study adds to the growing list of human 14-3-3-binding proteins and implicates a role for 14-3-3 proteins in a plethora of essential biological processes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
279
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
32046-54
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15161933-14-3-3 Proteins, pubmed-meshheading:15161933-Blotting, Western, pubmed-meshheading:15161933-Cell Cycle, pubmed-meshheading:15161933-Cell Separation, pubmed-meshheading:15161933-Chromatin, pubmed-meshheading:15161933-Chromatography, pubmed-meshheading:15161933-Chromatography, High Pressure Liquid, pubmed-meshheading:15161933-DNA, pubmed-meshheading:15161933-DNA Damage, pubmed-meshheading:15161933-Flow Cytometry, pubmed-meshheading:15161933-Glutathione Transferase, pubmed-meshheading:15161933-HeLa Cells, pubmed-meshheading:15161933-Humans, pubmed-meshheading:15161933-Interphase, pubmed-meshheading:15161933-Mass Spectrometry, pubmed-meshheading:15161933-Mitosis, pubmed-meshheading:15161933-Peptides, pubmed-meshheading:15161933-Precipitin Tests, pubmed-meshheading:15161933-Protein Binding, pubmed-meshheading:15161933-Protein Folding, pubmed-meshheading:15161933-Proteome, pubmed-meshheading:15161933-Proteomics, pubmed-meshheading:15161933-Recombinant Fusion Proteins, pubmed-meshheading:15161933-Transfection, pubmed-meshheading:15161933-Tyrosine 3-Monooxygenase
pubmed:year
2004
pubmed:articleTitle
Comprehensive proteomic analysis of interphase and mitotic 14-3-3-binding proteins.
pubmed:affiliation
Howard Hughes Medical Institute, Harvard University, Cambridge, Massachusetts 02138, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't