Covalent complex of phenylalanyl-tRNA synthetase with 4-thiouridine-substituted tRNA(Phe) gene transcript retains aminoacylation activity

FEBS Lett. 1998 May 1;427(1):1-4. doi: 10.1016/s0014-5793(98)00398-6.

Abstract

s4U-containing transcripts of tRNA(Phe) gene have been prepared by complete substitution of 16 U residues or by random incorporation of s4U residues followed by affinity electrophoresis isolation of s4U-monosubstituted tRNA transcripts. Both analogs have been cross-linked to Thermus thermophilus phenylalanyl-tRNA synthetase (PheRS) and the specificity of the cross-linking has been demonstrated. Functional activity of the covalent complex of PheRS with the s4U-monosubstituted transcript has been shown by aminoacylation of 60% of the enzyme-cross-linked tRNA. This is the first instance in which biological activity of aminoacyl-tRNA synthetase and cross-linked tRNA in a specific complex has been revealed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Nucleic Acid Conformation
  • Phenylalanine-tRNA Ligase / metabolism*
  • RNA, Transfer, Phe / chemistry
  • RNA, Transfer, Phe / metabolism*
  • Thermus thermophilus / metabolism
  • Thiouridine / chemistry

Substances

  • RNA, Transfer, Phe
  • Thiouridine
  • Phenylalanine-tRNA Ligase