Home LiteratureArticle Details
PMID: 9384530 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

RNA aptamers to the peptidyl transferase inhibitor chloramphenicol.

Chemistry & biology ·Vol. 4 ·No. 11 ·1997-11-00 ·Pages 833-43

Burke DH, Hoffman DC, Brown A, Hansen M, Pardi A, Gold L

Abstract

The problem of how macromolecules adopt specific shapes to recognize small molecules in their environment is readily addressed through in vitro selections (the SELEX protocol). RNA-antibiotic interactions are particularly attractive systems for study because they provide an opportunity to expand our understanding of molecular recognition by RNA and to facilitate ribosomal modeling. Specifically, the antibiotic chloramphenicol (Cam) naturally binds bacterial ribosomes in the 'peptidyl transferase loop' of 23S ribosomal RNA to inhibit peptide bond formation. We identified Cam-binding RNA molecules ('aptamers') from two independent initial random RNA populations. Boundary determinations, ribonuclease S1 sensitivity analyses and the activity of truncated minimal RNAs identified a structural motif that is shared by sequences from both selections. The pseudosymmetric motif consists of a highly conserved central helix of five to six base pairs flanked by A-rich bulges and additional helices. Addition of Cam prior to ribonuclease S1 protected nucleotides in the conserved cores from cleavage. Reselection from a pool of mutated variants of the minimal aptamer further refined the sequence requirements for binding. Finally, we used proton nuclear magnetic resonance (NMR) to establish a 1:1 RNA: Cam stoichiometry of the complex. Both the protection and NMR data both show that Cam stabilizes the active fold of this aptamer. There are many different RNA sequences that can bind Cam. The Cam aptamers that we examined have a well-defined secondary structure with a binding pocket that appears to be stabilized by Cam. This RNA motif superficially resembles the Cam-binding site in 23S rRNA, although further work is needed to establish the significance of these similarities.

MeSH Terms
Base Sequence Chloramphenicol/pharmacology Enzyme Inhibitors/chemistry,metabolism Kinetics Magnetic Resonance Spectroscopy Molecular Sequence Data Nucleic Acid Conformation Peptidyl Transferases/antagonists & inhibitors RNA/chemistry,metabolism RNA, Ribosomal, 23S/metabolism
Chemicals
Enzyme Inhibitors RNA, Ribosomal, 23S RNA Chloramphenicol Peptidyl Transferases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Burke D H
Department of Molecular, Cellular and Development Biology, University of Colorado, Boulder, CO 80309-0347, USA. dhburke@beagle.colorado.edu
Hoffman D C
Brown A
Hansen M
Pardi A
Gold L
Article Info
Journal
Chemistry & biology
Abbr.
Chem Biol
ISSN
1074-5521
Published
1997-11-00
Pages
833-43
Language
English
Region
United States
NLM ID
9500160
Subset
IM
Grants
NIAID NIH HHS · 1F32AI09361 · United States
NIAID NIH HHS · AI33098 · United States
NIGMS NIH HHS · GM19963 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com