Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme: Enzyme inhibitors which act by binding to substrate

Y. Hori, E. V. Bichenkova, A. N. Wilton, M. N. El-Attug, S. Sadat-Ebrahimi, T. Tanaka, Yo Kikuchi, M. Araki, Y. Sugiura, K. T. Douglas

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

2,2′-p-Phenylene bis[6-(4-methyl-1-piperazinyl)]benzimidazole, 2,2′-bis(3,5-dihydroxyphenyl)-6,6′-bis benzimidazole, and 2,2′-bis(4-hydroxyphenyl)-6,6′-bis benzimidazole are shown by UV-visible and fluorescence spectrophotometry to be strong ligands for tRNA, giving simple, hyperbolic binding isotherms with apparent dissociation constants in the micromolar range. Hydroxyl radical footprinting indicates that they may bind in the D and T loops. On the basis of this tRNA recognition as a rationale, they were tested as inhibitors of the processing of precursor tRNAs by the RNA subunit of Escherichia coli RNase P (M1 RNA). Preliminary studies show that inhibition of the processing of Drosophila tRNA precursor molecules by phosphodiester bond cleavage, releasing the extraneous 5′-portion of RNA and the mature tRNA molecule, was dependent on both the structure of the inhibitor and the structure of the particular tRNA precursor substrate for tRNAAla, tRNAVal, and tRNAHis. In more detailed followup using the tRNAHis precursor as the substrate, experiments to determine the concentration dependence of the reaction showed that inhibition took time to reach its maximum extent. I50 values (concentrations for 50% inhibition) were between 5.3 and 20.8 μM, making these compounds among the strongest known inhibitors of this ribozyme, and the first inhibitors of it not based on natural products. These compounds effect their inhibition by binding to the substrate of the enzyme reaction, making them examples of an unusual class of enzyme inhibitors. They provide novel, small-molecule, inhibitor frameworks for this endoribonuclease ribozyme.

Original languageEnglish
Pages (from-to)603-608
Number of pages6
JournalBiochemistry
Volume40
Issue number3
DOIs
Publication statusPublished - 2001 Jan 23
Externally publishedYes

Fingerprint

Ribonuclease P
Catalytic RNA
RNA Precursors
RNA, Transfer, His
Enzyme Inhibitors
Transfer RNA
RNA
Molecules
RNA, Transfer, Ala
RNA, Transfer, Val
Substrates
Processing
Endoribonucleases
Spectrophotometry
Biological Products
Hydroxyl Radical
Escherichia coli
Isotherms
Fluorescence Spectrometry
Fluorescence

ASJC Scopus subject areas

  • Biochemistry

Cite this

Hori, Y., Bichenkova, E. V., Wilton, A. N., El-Attug, M. N., Sadat-Ebrahimi, S., Tanaka, T., ... Douglas, K. T. (2001). Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme: Enzyme inhibitors which act by binding to substrate. Biochemistry, 40(3), 603-608. https://doi.org/10.1021/bi002378f

Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme : Enzyme inhibitors which act by binding to substrate. / Hori, Y.; Bichenkova, E. V.; Wilton, A. N.; El-Attug, M. N.; Sadat-Ebrahimi, S.; Tanaka, T.; Kikuchi, Yo; Araki, M.; Sugiura, Y.; Douglas, K. T.

In: Biochemistry, Vol. 40, No. 3, 23.01.2001, p. 603-608.

Research output: Contribution to journalArticle

Hori, Y, Bichenkova, EV, Wilton, AN, El-Attug, MN, Sadat-Ebrahimi, S, Tanaka, T, Kikuchi, Y, Araki, M, Sugiura, Y & Douglas, KT 2001, 'Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme: Enzyme inhibitors which act by binding to substrate', Biochemistry, vol. 40, no. 3, pp. 603-608. https://doi.org/10.1021/bi002378f
Hori, Y. ; Bichenkova, E. V. ; Wilton, A. N. ; El-Attug, M. N. ; Sadat-Ebrahimi, S. ; Tanaka, T. ; Kikuchi, Yo ; Araki, M. ; Sugiura, Y. ; Douglas, K. T. / Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme : Enzyme inhibitors which act by binding to substrate. In: Biochemistry. 2001 ; Vol. 40, No. 3. pp. 603-608.
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