Taylor K D, Goel R, Shirazi F H, Molepo M, Popovic P, Stewart D J, Wong P T
Ottawa Regional Cancer Centre, Canada.
Br J Cancer. 1995 Dec;72(6):1400-5. doi: 10.1038/bjc.1995.521.
The dynamic effect of cis-diamminedichloroplatinum(II) (DPP) and its aquated metabolite (DDP-OH) on a dimyristoylphosphatidylserine (DMPS) model membrane was investigated by pressure tuning vibrational spectroscopy. The native species (DDP-Cl) and the aquated species (DPP-OH) were both observed to bind to the carboxylate group of the serine as evidenced by a frequency shift of 1622-1620 cm-1. However, only DDP-OH was observed to bind to the phosphate group (PO(-)2). The binding of either drug to DMPS resulted in an increased pressure required to halt the reorientational fluctuations of the acyl chains, indicating that the distance between the chains were increased. The two drugs did not partition into the matrix of the hydrophobic section in the model membrane. Collectively, these data suggest that DDP-Cl and DDP-OH are capable of binding to the polar head group of DMPS, resulting in an enlargement of the area of the head and a subsequent increase in the intermolecular distance between the acyl chains.
通过压力调谐振动光谱研究了顺二氯二氨铂(II)(DPP)及其水合代谢物(DDP-OH)对二肉豆蔻酰磷脂酰丝氨酸(DMPS)模型膜的动态影响。观察到天然物种(DDP-Cl)和水合物种(DPP-OH)均与丝氨酸的羧酸盐基团结合,这由1622 - 1620 cm-1的频率偏移证明。然而,仅观察到DDP-OH与磷酸基团(PO(-)2)结合。两种药物与DMPS的结合均导致阻止酰基链重新取向波动所需的压力增加,表明链之间的距离增加。这两种药物未分配到模型膜疏水部分的基质中。总体而言,这些数据表明DDP-Cl和DDP-OH能够与DMPS的极性头部基团结合,导致头部面积增大以及随后酰基链之间分子间距离增加。