Engineered ribosomes with tethered subunits for expanding biological function

Abstract

Ribo-T is a ribosome with covalently tethered subunits where core 16S and 23S ribosomal RNAs form a single chimeric molecule. Ribo-T makes possible a functionally orthogonal ribosome–mRNA system in cells. Unfortunately, use of Ribo-T has been limited because of low activity of its original version. Here, to overcome this limitation, we use an evolutionary approach to select new tether designs that are capable of supporting faster cell growth and increased protein expression. Further, we evolve new orthogonal Ribo-T/mRNA pairs that function in parallel with, but independent of, natural ribosomes and mRNAs, increasing the efficiency of orthogonal protein expression. The Ribo-T with optimized designs is able to synthesize a diverse set of proteins, and can also incorporate multiple non-canonical amino acids into synthesized polypeptides. The enhanced Ribo-T designs should be useful for exploring poorly understood functions of the ribosome and engineering ribosomes with altered catalytic properties.

Document Details

Document Type
Pub Defense Publication
Publication Date
Sep 02, 2019
Source ID
10.1038/s41467-019-11427-y

Entities

People

  • Alexander S Mankin
  • Anne E. d’Aquino
  • Do Soon Kim
  • Emily M Fulk
  • Erik D. Carlson
  • Kim Hoang
  • Michael C Jewett
  • Teresa Szal

Organizations

  • David and Lucile Packard Foundation
  • Human Frontier Science Program
  • National Science Foundation
  • United States Department of Defense

Tags

Fields of Study

  • Biology
  • Computer science

Readers

  • Electrical Engineering
  • Systems Analysis and Design
  • Virology (or Medical Virology).