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C-labeled isotopolog synthesized using the same MIDA boronate building block-based total synthesis approach revealed that peridinin is completely embedded within and physically spans the hydrophobic core of POPC membranes, maximizing its effective molarity at the site of the targeted lipid peroxidation reactions. Alternatively, the widely used carotenoid astaxanthin is significantly less potent and was found to primarily localize extramembranously. Peridinin thus represents a promising and biophysically well-characterized starting point for the development of small molecule antilipoperoxidants that serve as more effective biological probes and/or therapeutics.
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Hannah M. S. Haley
University of Illinois Urbana-Champaign
Adam Greschek Hill
Alexander I. Greenwood
University of Cincinnati
Journal of the American Chemical Society
University of Illinois Urbana-Champaign
Illinois College
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Haley et al. (Tue,) studied this question.
synapsesocial.com/papers/6a0337a0f1675f581a756c94 — DOI: https://doi.org/10.1021/jacs.8b06933