| Literature DB >> 26513677 |
Yi Lei1, Dehui Kong1, Ryan Hili1.
Abstract
In vitro selection of nucleic acid polymers can readily deliver highly specific receptors and catalysts for a variety of applications; however, it is suspected that the functional group deficit of nucleic acids has limited their potential with respect to proteinogenic polymers. This has stimulated research toward expanding their chemical diversity to bridge the functional gap between nucleic acids and proteins to develop a superior biopolymer. In this study, we investigate the effect of codon library size and composition on the sequence specificity of T4 DNA ligase in the DNA-templated polymerization of both unmodified and modified oligonucleotides. Using high-throughput DNA sequencing of duplex pairs, we have uncovered a 256-membered codon set that yields sequence-defined modified ssDNA polymers in high yield and with high fidelity.Entities:
Keywords: DNA sequencing; DNA-templated; SELEX; T4 DNA ligase; aptamers
Mesh:
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Year: 2015 PMID: 26513677 DOI: 10.1021/acscombsci.5b00119
Source DB: PubMed Journal: ACS Comb Sci ISSN: 2156-8944 Impact factor: 3.784