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A Semisynthetic Approach to New Immunoadjuvant Candidates: Site‐Selective Chemical Manipulation of Escherichia coli Monophosphoryl Lipid A
Authors:Dr. Daniele D'Alonzo  Manuela Cipolletti  Giulia Tarantino  Marcello Ziaco  Dr. Giuseppina Pieretti  Prof. Alfonso Iadonisi  Prof. Giovanni Palumbo  Dr. Alberto Alfano  Dr. Mariateresa Giuliano  Prof. Mario De Rosa  Prof. Chiara Schiraldi  Dr. Marcella Cammarota  Prof. Michelangelo Parrilli  Dr. Emiliano Bedini  Prof. Maria M. Corsaro
Affiliation:1. Department of Chemical Sciences, University of Naples Federico?II, Naples, Italy;2. Department of Biology, University “Roma Tre”, Rome, Italy;3. Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff, The United Kingdom;4. Department of Experimental Medicine, Second University of Naples, Naples, Italy;5. Department of Biology, University of Naples Federico?II, Naples, Italy
Abstract:A semisynthetic approach to novel lipid A derivatives from Escherichia coli (E. coli) lipid A is reported. This methodology stands as an alternative to common approaches based exclusively on either total synthesis or extraction from bacterial sources. It relies upon the purification of the lipid A fraction from fed‐batch fermentation of E. coli, followed by its structural modification through tailored, site‐selective chemical reactions. In particular, modification of the lipid pattern and functionalization of the phosphate group as well as of the sole primary hydroxyl group were accomplished, highlighting the unusual reactivity of the molecule. Preliminary investigations of the immunostimulating activity of the new semisynthetic lipid A derivatives show that some of them stand out as promising, new immunoadjuvant candidates.
Keywords:carbohydrates  glycolipids  immunology  lipids  synthetic methods
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