» Articles » PMID: 20863807

A Modified Fluorescent Intercalator Displacement Assay for RNA Ligand Discovery

Overview
Journal Anal Biochem
Publisher Elsevier
Specialty Biochemistry
Date 2010 Sep 25
PMID 20863807
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Fluorescent intercalator displacement (FID) is a convenient and practical tool for identifying new nucleic acid-binding ligands. The success of FID is based on the fact that it can be fashioned into a versatile screening assay for assessing the relative binding affinities of compounds to nucleic acids. FID is a tagless approach; the target RNAs and the ligands or small molecules under investigation do not need to be modified in order to be examined. In this study, a modified FID assay for screening RNA-binding ligands was established using 3-methyl-2-((1-(3-(trimethylammonio)propyl)-4-quinolinylidene)methyl)benzothiazolium (TO-PRO) as the fluorescent indicator. Electrospray ionization mass spectrometry (ESI-MS) results provide direct evidence that correlates the reduction in fluorescence intensity observed in the FID assay with displacement of the dye molecule from RNA. The assay was successfully applied to screen a variety of RNA-binding ligands with a set of small hairpin RNAs. Ligands that bind with moderate affinity to the chosen RNA constructs (A-site, TAR [transactivation response element], h31 [helix 31], and H69 [helix 69] were identified.

Citing Articles

Design of deep-red emissive forced intercalation-induced light-up peptide as an indicator for the HIV-1 TAR RNA-ligand assay: integration of benzo[c,d]indole-quinoline (BIQ) cyanine dye into Tat peptide.

Ujuagu A, Sato Y, Lee E, Nishizawa S Anal Sci. 2024; 40(11):2089-2095.

PMID: 39102162 DOI: 10.1007/s44211-024-00642-3.


Large-scale analysis of small molecule-RNA interactions using multiplexed RNA structure libraries.

Nagasawa R, Onizuka K, Komatsu K, Miyashita E, Murase H, Ojima K Commun Chem. 2024; 7(1):98.

PMID: 38693284 PMC: 11865577. DOI: 10.1038/s42004-024-01181-8.


Contemporary Progress and Opportunities in RNA-Targeted Drug Discovery.

Garner A ACS Med Chem Lett. 2023; 14(3):251-259.

PMID: 36923915 PMC: 10009794. DOI: 10.1021/acsmedchemlett.3c00020.


A toolkit for the identification of NEAT1_2/paraspeckle modulators.

An H, Elvers K, Gillespie J, Jones K, Atack J, Grubisha O Nucleic Acids Res. 2022; 50(20):e119.

PMID: 36099417 PMC: 9723620. DOI: 10.1093/nar/gkac771.


Targeting RNA structures with small molecules.

Childs-Disney J, Yang X, Gibaut Q, Tong Y, Batey R, Disney M Nat Rev Drug Discov. 2022; 21(10):736-762.

PMID: 35941229 PMC: 9360655. DOI: 10.1038/s41573-022-00521-4.


References
1.
Ryu D, Rando R . Aminoglycoside binding to human and bacterial A-Site rRNA decoding region constructs. Bioorg Med Chem. 2001; 9(10):2601-8. DOI: 10.1016/s0968-0896(01)00034-7. View

2.
Rosu F, Gabelica V, Houssier C, De Pauw E . Determination of affinity, stoichiometry and sequence selectivity of minor groove binder complexes with double-stranded oligodeoxynucleotides by electrospray ionization mass spectrometry. Nucleic Acids Res. 2002; 30(16):e82. PMC: 134255. DOI: 10.1093/nar/gnf081. View

3.
Griffey R, Hofstadler S . Measuring dissociation constants of RNA and aminoglycoside antibiotics by electrospray ionization mass spectrometry. Anal Biochem. 2000; 280(2):264-71. DOI: 10.1006/abio.2000.4550. View

4.
Monchaud D, Allain C, Bertrand H, Smargiasso N, Rosu F, Gabelica V . Ligands playing musical chairs with G-quadruplex DNA: a rapid and simple displacement assay for identifying selective G-quadruplex binders. Biochimie. 2008; 90(8):1207-23. DOI: 10.1016/j.biochi.2008.02.019. View

5.
Lewis M, Long E . Fluorescent intercalator displacement analyses of DNA binding by the peptide-derived natural products netropsin, actinomycin, and bleomycin. Bioorg Med Chem. 2006; 14(10):3481-90. DOI: 10.1016/j.bmc.2006.01.006. View