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    Comparative gel-based phosphoproteomics in response to signaling molecules

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    Type
    Article
    Authors
    Marondedze, Claudius cc
    Lilley, Kathryn S.
    Thomas, Ludivine
    KAUST Department
    Biological and Environmental Sciences and Engineering (BESE) Division
    Bioscience Core Lab
    Bioscience Program
    Core Labs
    Date
    2013-09-03
    Permanent link to this record
    http://hdl.handle.net/10754/562964
    
    Metadata
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    Abstract
    The gel-based proteomics approach is a valuable technique for studying the characteristics of proteins. This technique has diverse applications ranging from analysis of a single protein to the study of the total cellular proteins. Further, protein quality and to some extent distribution can be first assessed by means of one-dimensional gel electrophoresis and then more informatively, for comparative analysis, using the two-dimensional gel electrophoresis technique. Here, we describe how to take advantage of the availability of fluorescent dyes to stain for a selective class of proteins on the same gel for the detection of both phospho- and total proteomes. This enables the co-detection of phosphoproteins as well as total proteins from the same gel and is accomplished by utilizing two different fluorescent stains, the ProQ-Diamond, which stains only phosphorylated proteins, and Sypro Ruby, which stains the entire subset of proteins. This workflow can be applied to gain insights into the regulatory mechanisms induced by signaling molecules such as cyclic nucleotides through the quantification and subsequent identification of responsive phospho- and total proteins. © Springer Science+Business Media New York 2013.
    Publisher
    Humana Press
    Journal
    Methods in Molecular Biology
    ISBN
    9781627034401
    DOI
    10.1007/978-1-62703-441-8-10
    PubMed ID
    23681577
    ae974a485f413a2113503eed53cd6c53
    10.1007/978-1-62703-441-8-10
    Scopus Count
    Collections
    Articles; Biological and Environmental Science and Engineering (BESE) Division; Bioscience Program; Bioscience Core Lab

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