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. 2010 Sep 29;39(3):936–948. doi: 10.1093/nar/gkq824

Figure 5.

Figure 5.

1H NMR spectroscopy on the G-quadruplex at BCL2 MBR. (A) NMR spectrum of the wild-type sequence (23 mer, GS) at 5°C. The spectrum was recorded on a Bruker Avance 800 MHz spectrometer with a cryo probe and analyzed by TOPSPIN 2.0 software. (B) NMR spectra recorded at different temperatures for GS. (C) NMR spectrum of the mutant with a 2-nt loop (G2 loop) at 5°C. In all the panels A–C, the resonance peaks between 10.8 and 12.2 ppm represent those resulting from the imino hydrogen present in the G-quadruplex structure. The resonance peaks at ∼13 and 14.5 ppm result from A…T and G…C Watson–Crick base pairing.