| Literature DB >> 27100911 |
Niancao Chen1, Xuechen Shi1, Yong Wang2.
Abstract
Natural polymers are synthesized and decomposed under physiological conditions. However, it is challenging to develop synthetic polymers whose formation and reversibility can be both controlled under physiological conditions. Here we show that both linear and branched DNA polymers can be synthesized via molecular hybridization in aqueous solutions, on the particle surface, and in the extracellular matrix (ECM) without the involvement of any harsh conditions. More importantly, these polymers can be effectively reversed to dissociate under the control of molecular triggers. Since nucleic acids can be conjugated with various molecules or materials, we anticipate that molecularly regulated reversible DNA polymerization holds potential for broad biological and biomedical applications.Entities:
Keywords: DNA; hybridization; polymers; reversible polymerization; self-assembly
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Year: 2016 PMID: 27100911 PMCID: PMC4884157 DOI: 10.1002/anie.201601008
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336