Lee O, Roberts G M, Diem M
Biopolymers. 1989 Oct;28(10):1759-70. doi: 10.1002/bip.360281009.
Infrared vibrational CD (VCD) of a small peptide, L-alanyl-L-alanyl-L-alanine (Ala3), and a peptide model, N-acetyl-L-alanine-N'-methyl-amide (AAMA), in the 1550-1750-cm-1 region has been observed. The "coupled oscillator" VCD feature observed for Ala3 in the amide I region is interpreted in terms of a solution structure stabilized by the electrostatic interaction of the zwitterionic groups. No such interactions are possible in basic aqueous solution of Ala3 nor in AAMA in neutral solution. Thus, the coupled oscillator features are lost in the latter two cases, indicating the absence of a simple stabilized conformation.
已观察到小肽L-丙氨酰-L-丙氨酰-L-丙氨酸(Ala3)和肽模型N-乙酰-L-丙氨酸-N'-甲基酰胺(AAMA)在1550 - 1750 cm⁻¹区域的红外振动圆二色性(VCD)。在酰胺I区域观察到的Ala3的“耦合振子”VCD特征,是根据两性离子基团的静电相互作用稳定的溶液结构来解释的。在Ala3的碱性水溶液中或在中性溶液中的AAMA中,不可能存在这样的相互作用。因此,在后两种情况下耦合振子特征消失,表明不存在简单的稳定构象。