Quantification of casein phosphorylation with conformational interpretation using Raman spectroscopy

Roger M. Jarvis, Ewan W. Blanch, Alexander P. Golovanov, James Screen, Royston Goodacre

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Raman spectroscopy is emerging as a powerful method for obtaining both quantitative and qualitative information from biological samples. One very interesting area of research, for which the technique has rarely been used, is the detection, quantification and structural analysis of post-translational modifications (PTMs) on proteins. Since Raman spectra can be used to address both of these questions simultaneously, we have developed near infrared Raman spectroscopy with appropriate chemometric approaches (partial least squares regression) to quantify low concentration (4 μM) mixtures of phosphorylated and dephosphorylated bovine αs-casein. In addition, we have used these data in conjunction with Raman optical activity (ROA) spectra and NMR to assess the structural changes that occur upon phosphorylation.© The Royal Society of Chemistry.
    Original languageEnglish
    Pages (from-to)1053-1060
    Number of pages7
    JournalAnalyst
    Volume132
    Issue number10
    DOIs
    Publication statusPublished - 2007

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