| Literature DB >> 27365192 |
Rosemary L Kanasty1,2, Arturo J Vegas2,3,4, Luke M Ceo2,3,4, Martin Maier5, Klaus Charisse5, Jayaprakash K Nair5, Robert Langer1,2,3,6,7,8, Daniel G Anderson9,10,11,12,13,14.
Abstract
The functionality of natural biopolymers has inspired significant effort to develop sequence-defined synthetic polymers for applications including molecular recognition, self-assembly, and catalysis. Conjugation of synthetic materials to biomacromolecules has played an increasingly important role in drug delivery and biomaterials. We developed a controlled synthesis of novel oligomers from hydroxyproline-based building blocks and conjugated these materials to siRNA. Hydroxyproline-based monomers enable the incorporation of broad structural diversity into defined polymer chains. Using a perfluorocarbon purification handle, we were able to purify diverse oligomers through a single solid-phase extraction method. The efficiency of synthesis was demonstrated by building 14 unique trimers and 4 hexamers from 6 diverse building blocks. We then adapted this method to the parallel synthesis of hundreds of materials in 96-well plates. This strategy provides a platform for the screening of libraries of modified biomolecules.Entities:
Keywords: bioconjugates; fluorous synthesis; oligomers; sequence-defined polymers; siRNA
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Year: 2016 PMID: 27365192 PMCID: PMC5245870 DOI: 10.1002/anie.201602748
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336