FRET enabled real time detection of RNA-small molecule binding

J Am Chem Soc. 2009 Dec 9;131(48):17605-14. doi: 10.1021/ja905767g.

Abstract

A robust analysis and discovery platform for antibiotics targeting the bacterial rRNA A-site has been developed by incorporating a new emissive U surrogate into the RNA and labeling the aminoglycosides with an appropriate fluorescence acceptor. Specifically, a 5-methoxyquinazoline-2,4(1H,3H)-dione-based emissive uracil analogue was identified to be an ideal donor for 7-diethylaminocoumarin-3-carboxylic acid. This donor/acceptor pair displays a critical Forster radius (R(0)) of 27 A, a value suitable for an A-site-aminoglycoside assembly. Titrating the coumarin labeled aminoglycosides into the emissive A-site construct, labeled at position U1406, shows a decrease in donor emission (at 395 nm) and concurrent increase of the acceptor emission (at 473 nm). Titration curves, obtained by fitting the donor's emission quenching or the augmentation of the acceptor's sensitized emission, faithfully generate EC(50) values. Titration of unlabeled ligands into the preformed FRET complex showed a continuous increase of the donor emission, with a concurrent decrease of the acceptor emission, yielding valuable data regarding competitive displacement of aminoglycosides by A-site binders. Detection of antibiotic binding is therefore not dependent on changes in the environment of a single fluorophore, but rather on the responsive interaction between two chromophores acting as a FRET pair, facilitating the determination of direct binding and competitive displacement events with FRET accuracy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aminoglycosides / metabolism
  • Base Sequence
  • Coumarins / metabolism
  • Drug Design
  • Fluorescence Resonance Energy Transfer*
  • Fluorescent Dyes / metabolism
  • Ligands
  • RNA / chemical synthesis
  • RNA / genetics
  • RNA / metabolism*
  • Time Factors
  • Uridine / metabolism

Substances

  • Aminoglycosides
  • Coumarins
  • Fluorescent Dyes
  • Ligands
  • RNA
  • coumarin
  • Uridine