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Quantitative proteomic analysis of yeast DNA replication proteins

Quantitative proteomic analysis of yeast DNA replication proteins

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Authors

  • Takashi Kubota
  • David A. Stead
  • Shin-ichiro Hiraga
  • Sara ten Have
  • Anne D. Donaldson

Research units

Info

Original languageEnglish
Pages196-202
Number of pages7
JournalMethods (San Diego, Calif.)
Journal publication date2012
Volume57
Issue2
DOIs
StatePublished

Abstract

Chromatin is dynamically regulated, and proteomic analysis of its composition can provide important information about chromatin functional components. Many DNA replication proteins for example bind chromatin at specific times during the cell cycle. Proteomic investigation can also be used to characterize changes in chromatin composition in response to perturbations such as DNA damage, while useful information is obtained by testing the effects on chromatin composition of mutations in chromosome stability pathways. We have successfully used the method of stable isotope labeling by amino acids in cell culture (SILAC) for quantitative proteomic analysis of normal and pathological changes to yeast chromatin. Here we describe this proteomic method for analyzing changes to Saccharomyces cerevisiae chromatin, illustrating the procedure with an analysis of the changes that occur in chromatin composition as cells progress from a G1 phase block (induced by alpha factor) into S phase (in the presence of DNA replication inhibitor hydroxyurea). (c) 2012 Elsevier Inc. All rights reserved.

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