The cis/trans conformational equilibrium of the two Ac-Pro isomers of the beta-turn model dipeptide [13C]-Ac-L-Pro-D-Ala-NHMe, 98% 13C enriched at the acetyl carbonyl atom, was investigated by the use of variable temperature gradient enhanced 1H-nmr, two-dimensional (2D) 1H,1H nuclear Overhauser eff
Variable-temperature and pH studies of a DNA minor groove binder, Hoechst 32985, by 1H NMR spectroscopy
✍ Scribed by Keith J. Cross; Kevin J. Embrey; Murray Coles; Wendy Bicknell; David J. Craik
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 772 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H NMR spectra of the dipiperazine‐based DNA minor groove binding compound Hoechst 32985 indicate that at room temperature and low pH (2.90) a single conformation is detected. This is attributed to the form in which both piperazine rings are protonated at the N‐methyl and the bulky methyl and aromatic groups are in an equatorial arrangement. The aliphatic regions of the spectra broaden considerably with an increase in either temperature or pH, indicating the presence of a dynamic exchange process. This process results in interchange of axial and equatorial environments of the piperazine ring protons and is attributed to combined ring and nitrogen inversions. Analysis of the variable‐temperature spectra for a solution at pH 2.90 allowed a Gibb's free energy of activation (Δ__G__‡) of 69.4±0.4 kJ mol^−1^ to be calculated for this process.
📜 SIMILAR VOLUMES