This review article by Jean-Jacques Vasseur, François Morvan, Yann Chevolot and colleagues from France looks at the design and applications of DNA glycoclusters and DNA-based carbohydrate microarrays, combining the automated chemistry of DNA and “click” chemistry.
The authors illustrate that DNA chemistry (phosphoramidite as well as H-phosphonate) can be used to synthesis glycomimetics via a very efficient copper(I) catalyzed azide alkyne cycloaddition (“click” chemistry). This gives quick access to a range of glycomimetics with different topologies, such as linear and crown-like. Due to the DNA tag present, the glycomimetics can easily be immobilized on microarrays to analyse their interactions and binding-properties with lectins. The authors demonstrate that DNA glycoarrays relying on DNA directed immobilization presents several advantages over conventional immobilization techniques.
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DNA glycoclusters and DNA-based carbohydrate microarrays: From design to applications, François Morvan, Sébastien Vidal, Eliane Souteyrand, Yann Chevolot and Jean-Jacques Vasseur, RSC Adv., 2012, DOI: 10.1039/C2RA21550K
This article is part of a web-themed issue accross RSC Advances, ChemComm and Organic & Biomolecular Chemistry ‘Nucleic acids: new life, new materials‘ dedicated to the memory of Professor Har Gobind Khorana (1922 – 2011), acknowledging his legacy to the nucleic acids community. Read the collection so far here.