Regulation of Protein Activity and Cellular Functions Mediated by Molecularly Evolved Nucleic Acids

Angew Chem Int Ed Engl. 2019 Feb 4;58(6):1621-1625. doi: 10.1002/anie.201809010. Epub 2019 Jan 14.

Abstract

Regulation of protein activity is essential for revealing the molecular mechanisms of biological processes. DNA and RNA achieve many uniquely efficient functions, such as genetic expression and regulation. The chemical capability to synthesize artificial nucleotides can expand the chemical space of nucleic acid libraries and further increase the functional diversity of nucleic acids. Herein, a versatile method has been developed for modular expansion of the chemical space of nucleic acid libraries, thus enabling the generation of aptamers able to regulate protein activity. Specifically, an aptamer that targets integrin alpha3 was identified and this aptamer can inhibit cell adhesion and migration. Overall, this chemical-design-assisted in vitro selection approach enables the generation of functional nucleic acids for elucidating the molecular basis of biological activities and uncovering a novel basis for the rational design of new protein-inhibitor pharmaceuticals.

Keywords: aptamers; cell adhesion; inhibitors; membrane proteins; molecular evolution.

Publication types

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

MeSH terms

  • Aptamers, Nucleotide / chemistry
  • Aptamers, Nucleotide / metabolism
  • Aptamers, Nucleotide / pharmacology
  • Cell Adhesion / drug effects
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • DNA / chemistry
  • DNA / metabolism*
  • Humans
  • Integrin alpha3 / chemistry
  • Integrin alpha3 / metabolism*
  • Molecular Structure
  • RNA / chemistry
  • RNA / metabolism*

Substances

  • Aptamers, Nucleotide
  • Integrin alpha3
  • RNA
  • DNA