13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      DNA-Encoded Chemical Libraries: A Selection System Based on Endowing Organic Compounds with Amplifiable Information

      1 , 2
      Annual Review of Biochemistry
      Annual Reviews

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          <p class="first" id="P1">The discovery of organic ligands that bind specifically to proteins is a central problem in chemistry, biology and biomedical sciences. The encoding of individual organic molecules with distinctive DNA tags, serving as amplifiable identification barcodes, allows the construction and screening of combinatorial libraries of unprecedented size, thus facilitating the discovery of ligands to many different protein targets. Fundamentally, one links powers of genetics and chemical synthesis. After the initial description of DNA-encoded chemical libraries in 1992, several experimental embodiments of the technology have been reduced to practice. This review provides an historical account on important milestones for the development of DNA-encoded chemical libraries, a survey of relevant on-going research activities and a glimpse into the future. </p>

          Related collections

          Most cited references82

          • Record: found
          • Abstract: not found
          • Article: not found

          Functionalizing nanoparticles with biological molecules: developing chemistries that facilitate nanotechnology.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Design, synthesis and selection of DNA-encoded small-molecule libraries.

            Biochemical combinatorial techniques such as phage display, RNA display and oligonucleotide aptamers have proven to be reliable methods for generation of ligands to protein targets. Adapting these techniques to small synthetic molecules has been a long-sought goal. We report the synthesis and interrogation of an 800-million-member DNA-encoded library in which small molecules are covalently attached to an encoding oligonucleotide. The library was assembled by a combination of chemical and enzymatic synthesis, and interrogated by affinity selection. We describe methods for the selection and deconvolution of the chemical display library, and the discovery of inhibitors for two enzymes: Aurora A kinase and p38 MAP kinase.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              DNA-encoded chemistry: enabling the deeper sampling of chemical space

              DNA-encoded chemistry enables rapid and inexpensive syntheses and screening of vast chemical libraries, and is generating substantial interest and investment in the pharmaceutical industry. Here, Goodnow and colleagues provide an overview of the steps involved in the generation of DNA-encoded libraries, highlighting key applications and future directions for this technology.
                Bookmark

                Author and article information

                Journal
                Annual Review of Biochemistry
                Annu. Rev. Biochem.
                Annual Reviews
                0066-4154
                1545-4509
                June 20 2018
                June 20 2018
                : 87
                : 1
                : 479-502
                Affiliations
                [1 ]Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH Zürich), 8093 Zürich, Switzerland;
                [2 ]Department of Chemistry, The Scripps Research Institute, La Jolla, California 92037, USA;
                Article
                10.1146/annurev-biochem-062917-012550
                6080696
                29328784
                5874b70e-8cd6-4161-93ad-31219787d9df
                © 2018
                History

                Comments

                Comment on this article