Quantitative proteomic analysis of yeast DNA replication proteins

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

    Research output: Contribution to journalArticle

    13 Citations (Scopus)

    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.

    Original languageEnglish
    Pages (from-to)196-202
    Number of pages7
    JournalMethods (San Diego, Calif.)
    Volume57
    Issue number2
    DOIs
    Publication statusPublished - 2012

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