A novel FRET pair for detection of parallel DNA triplexes by the LightCycler

BMC Biotechnology

Methodology Article

Imrich Géci¹  Erik B Pedersen¹  Uffe V Schneider²  Jette K Severinsen²  Nina Jøhnk²  Limei M Okkels²  Nikolaj D Mikkelsen²  Teena Klinge²  Gorm Lisby²  Henrik Westh³ 

[1] Nucleic Acid Center and Department of Chemistry, University of Southern Denmark, Campusvej 55, 5230, Odense M, Denmark;QuantiBact Inc, Department of Clinical Microbiology, Hvidovre Hospital, Kettegaards Alle 30, 2650, Hvidovre, Denmark;QuantiBact Inc, Department of Clinical Microbiology, Hvidovre Hospital, Kettegaards Alle 30, 2650, Hvidovre, Denmark;Department of Clinical Microbiology, Hvidovre Hospital, Kettegaards Alle 30, 2650, Hvidovre, Denmark;Faculty of Health, University of Copenhagen, Copenhagen, Denmark;

关键词: High Performance Liquid Chromatography;    Fluorescence Resonance Energy Transfer;    Sodium Acetate Buffer;    Sodium Cacodylate Buffer;    Melting Point Determination;   

DOI  :  10.1186/1472-6750-10-4

 received in 2009-07-01, accepted in 2010-01-27,  发布年份 2010

来源: Springer

【 摘 要 】

BackgroundMelting temperature of DNA structures can be determined on the LightCycler using quenching of FAM. This method is very suitable for pH independent melting point (Tm) determination performed at basic or neutral pH, as a high throughput alternative to UV absorbance measurements. At acidic pH quenching of FAM is not very suitable, since the fluorescence of FAM is strongly pH dependent and drops with acidic pH.Hoogsteen based parallel triplex helix formation requires protonation of cytosines in the triplex forming strand. Therefore, nucleic acid triplexes show strong pH dependence and are stable only at acidic pH. This led us to establish a new pH independent fluorophore based measuring system on the LightCycler for thermal stability studies of parallel triplexes.ResultsA novel LightCycler FRET pair labelled with ATTO495 and ATTO647N was established for parallel triplex detection with antiparallel duplex as a control for the general applicability of these fluorophores for Tm determination. The ATTO fluorophores were pH stable from pH 4.5 to 7.5. Melting of triplex and duplex structures were accompanied by a large decrease in fluorescence intensity leading to well defined Tm and high reproducibility. Validation of Tm showed low intra- and inter-assay coefficient of variation; 0.11% and 0.14% for parallel triplex and 0.19% and 0.12% for antiparallel duplex. Measurements of Tm and fluorescence intensity over time and multiple runs showed great time and light stability of the ATTO fluorophores. The variance on Tm determinations was significant lower on the LightCycler platform compared to UV absorbance measurements, which enable discrimination of DNA structures with very similar Tm. Labelling of DNA probes with ATTO fluorophore increased Tm of antiparallel duplexes significantly, but not Tm of parallel triplexes.ConclusionsWe have established a novel pH independent FRET pair with high fluorescence signals on the LightCycler platform for both antiparallel duplex and parallel triplex formation. The method has been thoroughly validated, and is characterized by an excellent accuracy and reproducibility. This FRET pair is especially suitable for ΔTm and Tm determinations of pH dependent parallel triplex formation.

【 授权许可】

CC BY   
© Schneider et al; licensee BioMed Central Ltd. 2010