Utilization of alkyne bioconjugations to modulate protein function

Bioorg Med Chem Lett. 2017 Jan 1;27(1):30-33. doi: 10.1016/j.bmcl.2016.11.041. Epub 2016 Nov 16.

Abstract

The ability to introduce or modify protein function has widespread application to multiple scientific disciplines. The introduction of unique unnatural amino acids represents an excellent mechanism to incorporate new functionality; however, this approach is limited by ability of the translational machinery to recognize and incorporate the chemical moiety. To overcome this potential limitation, we aimed to exploit the functionality of existing unnatural amino acids to perform bioorthogonal reactions to introduce the desired protein modification, altering its function. Specifically, via the introduction of a terminal alkyne containing unnatural amino acid, we demonstrated chemically programmable protein modification through the Glaser-Hay coupling to other terminal alkynes, altering the function of a protein. In a proof-of-concept experiment, this approach has been utilized to modify the fluorescence spectrum of green fluorescent protein.

Keywords: Bioconjugations; Glaser-Hay reaction; Green fluorescent protein; Unnatural amino acids.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Amino Acids / chemistry*
  • Green Fluorescent Proteins / chemistry
  • Green Fluorescent Proteins / metabolism*
  • Models, Molecular
  • Molecular Structure

Substances

  • Alkynes
  • Amino Acids
  • Green Fluorescent Proteins