DNA Display I. Sequence-Encoded Routing of DNA Populations
Open Access
- 22 June 2004
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLoS Biology
- Vol. 2 (7) , e173
- https://doi.org/10.1371/journal.pbio.0020173
Abstract
Recently reported technologies for DNA-directed organic synthesis and for DNA computing rely on routing DNA populations through complex networks. The reduction of these ideas to practice has been limited by a lack of practical experimental tools. Here we describe a modular design for DNA routing genes, and routing machinery made from oligonucleotides and commercially available chromatography resins. The routing machinery partitions nanomole quantities of DNA into physically distinct subpools based on sequence. Partitioning steps can be iterated indefinitely, with worst-case yields of 85% per step. These techniques facilitate DNA-programmed chemical synthesis, and thus enable a materials biology that could revolutionize drug discovery.Keywords
This publication has 21 references indexed in Scilit:
- DNA Display III. Solid-Phase Organic Synthesis on Unprotected DNAPLoS Biology, 2004
- DNA Display II. Genetic Manipulation of Combinatorial Chemistry Libraries for Small-Molecule EvolutionPLoS Biology, 2004
- Solution of a 20-Variable 3-SAT Problem on a DNA ComputerScience, 2002
- The Generality of DNA-Templated Synthesis as a Basis for Evolving Non-Natural Small MoleculesJournal of the American Chemical Society, 2001
- Mutation Typing Using Electrophoresis and Gel-Immobilized Acrydite TM ProbesBioTechniques, 1998
- Production of Single-Stranded DNA Using a Uracil-N-glycosylase-Mediated Asymmetric Polymerase Chain Reaction MethodAnalytical Biochemistry, 1997
- Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar–coding strategyNature Genetics, 1996
- Rapid preparation of single stranded DNA from PCR products by streptavidin induced electrophoretic mobility shiftNucleic Acids Research, 1996
- Nucleic acid sequence-based amplificationNature, 1991
- Purification of Biologically Active Globin Messenger RNA by Chromatography on Oligothymidylic acid-CelluloseProceedings of the National Academy of Sciences, 1972