Niu C, Bertrand R D, Shindo H, Cohen J S
J Biochem Biophys Methods. 1979 Jul;1(3):135-43. doi: 10.1016/0165-022x(79)90032-0.
Comparative 13C--15N coupling constants are reported for the linear dipeptide tBoc-L-[U-13C]Ala-[15N]GlyOMe and the corresponding cyclic diketopiperazine, both in dimethylsulfoxide (DMSO) and, upon removal of the tBoc group, in water solutions. Spectra were obtained by 13C NMR and by the first application of J cross-polarization (JCP) 15N NMR, which greatly reduces the time required to accumulate 15N NMR spectra. In DMSO there was evidence for the formation of complexed species which were not present in water. The values obtained for the cross-peptide bond coupling constant 2J13C alpha--15N were consistently less (by 2.2 Hz in DMSO, 4.3 Hz in water) for the cyclic than for the linear peptide, which may be related to the cross-peptide bond conformation. The 15N resonance for the cyclic peptide was shifted only 2 ppm downfield from the linear peptide chemical shift value in both solvents.
报道了线性二肽叔丁氧羰基-L-[U-¹³C]丙氨酸-[¹⁵N]甘氨酸甲酯以及相应的环状二酮哌嗪在二甲基亚砜(DMSO)中,以及在去除叔丁氧羰基后在水溶液中的¹³C-¹⁵N耦合常数比较结果。光谱通过¹³C NMR以及首次应用J交叉极化(JCP)¹⁵N NMR获得,这大大减少了积累¹⁵N NMR光谱所需的时间。在DMSO中,有证据表明形成了在水中不存在的络合物种。环状肽的交叉肽键耦合常数²J¹³Cα-¹⁵N值始终比线性肽小(在DMSO中为2.2 Hz,在水中为4.3 Hz),这可能与交叉肽键构象有关。在两种溶剂中,环状肽的¹⁵N共振仅比线性肽化学位移值低场移动2 ppm。