Sequence‐Defined Oligomers from Hydroxyproline Building Blocks for Parallel Synthesis Applications. Issue 33 (1st July 2016)
- Record Type:
- Journal Article
- Title:
- Sequence‐Defined Oligomers from Hydroxyproline Building Blocks for Parallel Synthesis Applications. Issue 33 (1st July 2016)
- Main Title:
- Sequence‐Defined Oligomers from Hydroxyproline Building Blocks for Parallel Synthesis Applications
- Authors:
- Kanasty, Rosemary L.
Vegas, Arturo J.
Ceo, Luke M.
Maier, Martin
Charisse, Klaus
Nair, Jayaprakash K.
Langer, Robert
Anderson, Daniel G. - Abstract:
- 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. Abstract : Another link in the chain : A controlled synthesis of novel oligomers from hydroxyproline‐based building blocks was developed. The hydroxyproline‐based monomer allows the incorporation of diverse side chains, and high‐throughput purification can be achieved by fluorous solid‐phase extraction. This method is adaptable to high‐throughput synthesis in multiwell plates, thus allowing hundreds of novel oligomer structures to be synthesized inAbstract: 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. Abstract : Another link in the chain : A controlled synthesis of novel oligomers from hydroxyproline‐based building blocks was developed. The hydroxyproline‐based monomer allows the incorporation of diverse side chains, and high‐throughput purification can be achieved by fluorous solid‐phase extraction. This method is adaptable to high‐throughput synthesis in multiwell plates, thus allowing hundreds of novel oligomer structures to be synthesized in parallel. … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 55:Issue 33(2016)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 55:Issue 33(2016)
- Issue Display:
- Volume 55, Issue 33 (2016)
- Year:
- 2016
- Volume:
- 55
- Issue:
- 33
- Issue Sort Value:
- 2016-0055-0033-0000
- Page Start:
- 9529
- Page End:
- 9533
- Publication Date:
- 2016-07-01
- Subjects:
- bioconjugates -- fluorous synthesis -- oligomers -- sequence-defined polymers -- siRNA
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201602748 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8309.xml