Related Experiment Video
Updated: Jun 18, 2026

Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
Published on: June 19, 2018
Identification of single-base mismatches in duplex DNA by EPR spectroscopy
Pavol Cekan1, Snorri Th Sigurdsson
1University of Iceland, Science Institute, Dunhaga 3, 107 Reykjavik, Iceland.
Abstract:
The spin-labeled nucleoside (T)C, containing 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) conjugated to the exocyclic amino group of C, was used to detect single-base mismatches in duplex DNA for the first time by electron paramagnetic resonance (EPR) spectroscopy. Furthermore, the EPR spectra of the fully base-paired duplex ((T)C.G) and the mismatches ((T)C.A, (T)C.C, and (T)C.T) were significantly different, showing that the probe can identify its base-pairing partner in DNA. At lower pH, the mobility of (T)C.A, (T)C.C, and (T)C.T became higher, consistent with increased protonation of the mismatched pairs. Although the duplexes for each of the three flanking sequences tested gave distinguishable EPR signals, the best discrimination between base pairs was achieved for sequences containing a flanking A.T base pair, in particular 5'-d(G(T)CA) and 5'-d(T(T)CA). This study shows that minor structural variations in nucleic acids can be detected with carefully chosen spin labels in conjunction with EPR spectroscopy.
Related Concept Videos
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
Long-patch Base Excision Repair
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

