Investigation of polypeptide conformational transitions with two-dimensional Raman optical activity correlation analysis, applying autocorrelation and moving window approaches

L. Ashton, E. W. Blanch

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The study of conformational transitions in polypeptides is not only important for the understanding of folding mechanisms responsible for the self-assembly of proteins but also for the investigation of the misfolding of proteins that can result in diseases including cystic fibrosis, Alzheimer's, and Parkinson's diseases. Our recent studies developing twodimensional Raman optical activity (ROA) correlation analysis have proven to be successful in the investigation of polypeptide conformational transitions. However, the complexity of the ROA spectra, and the 2D correlation synchronous and asynchronous plots, makes data analysis detailed and complex, requiring great care in interpretation of 2D correlation rules. By utilizing the 2D correlation approaches of autocorrelation and moving windows it has been possible to gain further information from the ROA spectral data sets in a simpler and more consistent way. The most significant spectral intensity changes have been easily identified, facilitating appropriate interpretation of synchronous plots, and transition phases have been identified in the moving window plots, directly relating spectral intensity changes to the perturbation. © 2008 Society for Applied Spectroscopy.
    Original languageEnglish
    Pages (from-to)469-475
    Number of pages6
    JournalApplied Spectroscopy
    Volume62
    Issue number5
    DOIs
    Publication statusPublished - May 2008

    Keywords

    • Conformational transitions
    • Pol(L-glutamic acid)
    • Poly(L-lysine)
    • Raman optical activity
    • ROA
    • Two-dimensional correlation

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