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Photoswitchable precision glycooligomers and their lectin binding

The synthesis of photoswitchable glycooligomers is presented by applying solid-phase polymer synthesis and functional building blocks. The obtained glycoligands are monodisperse and present azobenzene moieties as well as sugar ligands at defined positions within the oligomeric backbone and side chai...

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Detalles Bibliográficos
Autores principales: Ponader, Daniela, Igde, Sinaida, Wehle, Marko, Märker, Katharina, Santer, Mark, Bléger, David, Hartmann, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143111/
https://www.ncbi.nlm.nih.gov/pubmed/25161717
http://dx.doi.org/10.3762/bjoc.10.166
Descripción
Sumario:The synthesis of photoswitchable glycooligomers is presented by applying solid-phase polymer synthesis and functional building blocks. The obtained glycoligands are monodisperse and present azobenzene moieties as well as sugar ligands at defined positions within the oligomeric backbone and side chains, respectively. We show that the combination of molecular precision together with the photoswitchable properties of the azobenzene unit allows for the photosensitive control of glycoligand binding to protein receptors. These stimuli-sensitive glycoligands promote the understanding of multivalent binding and will be further developed as novel biosensors.