| Literature DB >> 26580227 |
Spencer Carson1, Scott T Wick2, Peter A Carr2, Meni Wanunu1,3, Carlos A Aguilar2.
Abstract
Synthetic nucleic acids offer rich potential to understand and engineer new cellular functions, yet an unresolved limitation in their production and usage is deleterious products, which restrict design complexity and add cost. Herein, we employ a solid-state nanopore to differentiate molecules of a gene synthesis reaction into categories of correct and incorrect assemblies. This new method offers a solution that provides information on gene synthesis reactions in near-real time with higher complexity and lower costs. This advance can permit insights into gene synthesis reactions such as kinetics monitoring, real-time tuning, and optimization of factors that drive reaction-to-reaction variations as well as open venues between nanopore-sensing, synthetic biology, and DNA nanotechnology.Entities:
Keywords: DNA; HIV protease; single molecule; synthetic biology; translocation
Mesh:
Substances:
Year: 2015 PMID: 26580227 PMCID: PMC5154552 DOI: 10.1021/acsnano.5b05782
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881