Polyethylene glycol molecular crowders enhance the catalytic ability of bimolecular bacterial RNase P ribozymes

Md Sohanur Rahman, Mst Ara Gulshan, Shigeyoshi Matsumura, Yoshiya Ikawa*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The modular structure of bacterial ribonuclease P (RNase P) ribozymes, which recognize tertiary structures of precursor tRNAs (pre-tRNAs) to cleave their 5′ leader sequence, can be dissected physically into the two structured domain RNAs (S-domain and C-domain). Separately prepared S-domain RNA and C-domain RNA assemble to form bimolecular forms of RNase P ribozymes. We analyzed the effects of polyethylene glycols (PEGs) on pre-tRNA cleavage catalyzed by bimolecular RNase P ribozymes to examine the effects of molecular crowding on the reaction. PEG molecular crowders significantly enhanced the activities of bimolecular RNase P ribozymes, some of which were hardly active without PEGs.

Original languageEnglish
Pages (from-to)715-729
Number of pages15
JournalNucleosides, Nucleotides and Nucleic Acids
Volume39
Issue number5
DOIs
StatePublished - 2020/05/03

Keywords

  • Modular structure
  • RNA domain
  • molecular crowding
  • ribonuclease P
  • ribozyme
  • tRNA

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Genetics

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