Huang Jia-dong, Song Zhao, Li Jing, Wu Bao-yan, Yin Hui-jun, Chen Ke-ji, Chen Qiang
College of Life Sciences, Nankai University, Tianjin, China.
Chin J Integr Med. 2005 Mar;11(1):37-40. doi: 10.1007/BF02835747.
To study the targeted point and mechanism of the function of the blood-activating and stasis-removing Chinese drugs, Paeoniae Radix 801(PR801) in its cardiovascular protective effects and its specific binding with endothelin 1 (ET-1) as well as the dynamics of the two's interactive function by means of using affinity biosensors: IAsys Plus and quartz crystal microbalance (IAQCM).
ET-1 was immobilized on the surfaces of IAQCM by using the new surface modification methods. The PR801 in the solution was detected by modified substrates and the specific binding between PR801 and ET-1 was studied.
The curves went up or down after adding PR801. There is specific binding between PR801 and ET-1. The bound mass were 0.458 ng/mm(2) and 133.54 ng/cm(2), respectively. There exists relatively good stability with these two methods.
The affinity biosensors: IAQCM can be used to study the interaction mechanism between PR801 and ET-1, providing a new way to study the interaction mechanism of TCM. PR801 can bind ET-1 specifically in the experiments. Therefore, ET-1 is another target that PR801 can bind specifically besides thromboxane A(2).
采用亲和生物传感器IAsys Plus和石英晶体微天平(IAQCM),研究活血化瘀中药赤芍801(PR801)心血管保护作用的靶点和机制,及其与内皮素1(ET-1)的特异性结合以及二者相互作用的动力学。
采用新的表面修饰方法将ET-1固定在IAQCM表面,用修饰后的底物检测溶液中的PR801,研究PR801与ET-1的特异性结合。
加入PR801后曲线上升或下降,PR801与ET-1存在特异性结合,结合量分别为0.458 ng/mm²和133.54 ng/cm²,两种方法均具有较好的稳定性。
亲和生物传感器IAQCM可用于研究PR801与ET-1的相互作用机制,为研究中药相互作用机制提供了新途径。在实验中PR801能特异性结合ET-1,因此ET-1是PR801除血栓素A2外另一个能特异性结合的靶点。