arrow grid linear view icon
The College of Arts Sciences Search

You are here

David Usher

Associate Professor

Baker Laboratory, Room 350
dau1@cornell.edu
607-255-7063

Educational Background

  • PhD, University of Cambridge
  • MSc, Victoria University of Wellington

Overview

The Usher Group is studying the formation of the peptide bond using aminoacyl carrier oligonucleotides and a simple template oligomer.

Keywords

Chemical evolution, sequence specific reactions of nucleid acids, phosphate esters

Departments/Programs

  • Chemistry and Chemical Biology

Graduate Fields

  • Chemistry and Chemical Biology

Research

Dr. Usher's group has made a new amide-linked oligonucleotide analog which retains the furanose rings of natural nucleic acids but which uses three atoms to span the distance between sugar rings instead of the four found in naturally-occurring RNA and DNA. Two dimers, UNHU and ANHA, containing the novel amide linkage have been synthesized, and the latter has been shown to bind to poly(U). The group now plans to study solid-support synthesis of specific sequences, binding specificity, template reactions, and diagnostic and therapeutic applications of these analogs.

Discoveries made during the last fifteen years have revolutionized our understanding of the diverse roles that RNA plays in biological systems. However, methodologies for the chemical synthesis of oligoribonucleotides on solid phase supports have not kept pace with advances in DNA synthesis. Dr. Usher's group has developed a new type of 2'-hydroxyl protecting group for the automated machine synthesis of RNA oligomers: a 2-hydroxyisophthalate formaldehyde acetal (HIFA). The unique feature of this protecting group is that as the bis ester it is relatively stable to the acidic conditions that are used for repeated removal of dimethoxytrityl groups during chain elongation. However, the final deprotection step in alkali, which cleaves the chain from the support and removes the base and phosphate protecting groups, converts it to the bis carboxylate, and this can be removed relatively rapidly by treatment with mild acid. They are now modifying the isophthalate ring to increase the rate of acid- catalyzed deprotection. Other research interests are site-specific reactions of nucleic acids, mechanisms of phosphate ester hydrolysis, reactions on oligonucleotide templates, and the de novo synthesis of RNA under simulated prebiotic conditions.Naturally-occurring RNAAmide-linked analog.

Publications

  • McHale, A. H.; Usher, D. A. Hydrolytic stability of helical RNA: A selective advantage for the natural 3',5' bond. Proc. Natl. Acad. Sci. U.S.A. 1976, 73, 1149.
  • Ferris, J. P.; Usher D. A. Origin of life, in Biochemistry, 2nd ed. Zubay, G., ed., Macmillan: New York, 1988.
  • Rastogi, H.; Usher, D. A. A new 2'-hydroxyl protecting group for the automated synthesis of oligoribonucleotides. Nucleic Acids Res. 1995, 23, 4872.
  • Harris, M.; Usher, D. A. A new amide-linked polynucleotide analog. Origins Life Evol. Biosphere 1996, 26, 398.
  • Before Antisense. Antisense and Nucleic Acid Drug Development 1997, 7, 445.