A Quantitative Method for Evaluating the Stabilities of Nucleic Acids

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 96; no. 11; pp. 6113 - 6118
• Main Authors: Gelfand, Craig A., Plum, G. Eric, Mielewczyk, Slawomir, Remeta, David P., Breslauer, Kenneth J.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences of the United States of America 25-05-1999; National Acad Sciences; National Academy of Sciences; The National Academy of Sciences
• Subjects: Base Sequence; Biochemistry; Biological Sciences; DNA; DNA - chemistry; Drug Stability; Dyes; Energy Transfer; Energy value; Fluorescence; Fluorescent Dyes; Free energy; Kinetics; Nucleic Acid Conformation; Nucleic acids; Oligodeoxyribonucleotides - chemical synthesis; Oligodeoxyribonucleotides - chemistry; Oligonucleotides; Spectrometry, Fluorescence - methods; Thermodynamics; Titration
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.96.11.6113

We report a general method for screening, in solution, the impact of deviations from canonical Watson-Crick composition on the thermodynamic stability of nucleic acid duplexes. We demonstrate how fluorescence resonance energy transfer (FRET) can be used to detect directly free energy differences between an initially formed "reference" duplex (usually a Watson-Crick duplex) and a related "test" duplex containing a lesion/alteration of interest (e.g., a mismatch, a modified, a deleted, or a bulged base, etc.). In one application, one titrates into a solution containing a fluorescently labeled, FRET-active, reference duplex, an unlabeled, single-stranded nucleic acid (test strand), which may or may not compete successfully to form a new duplex. When a new duplex forms by strand displacement, it will not exhibit FRET. The resultant titration curve (normalized fluorescence intensity vs. logarithm of test strand concentration) yields a value for the difference in stability (free energy) between the newly formed, test strand-containing duplex and the initial reference duplex. The use of competitive equilibria in this assay allows the measurement of equilibrium association constants that far exceed the magnitudes accessible by conventional titrimetric techniques. Additionally, because of the sensitivity of fluorescence, the method requires several orders of magnitude less material than most other solution methods. We discuss the advantages of this method for detecting and characterizing any modification that alters duplex stability, including, but not limited to, mutagenic lesions. We underscore the wide range of accessible free energy values that can be defined by this method, the applicability of the method in probing for a myriad of nucleic acid variations, such as single nucleotide polymorphisms, and the potential of the method for high throughput screening.