Molecular dynamics simulation studies of transmembrane transport of chemical components in Chinese herbs and the function of platycodin D in a biological membrane

作     者：Shufang Yang Haiou Ding Ran Wang Xingxing Dai Xinyuan Shi Yanjiang Qiao 

作者机构：School of Chinese Materia MedicaBeijing University of Chinese MedicineBeijing 102488China School of Traditional Chinese MedicineCapital Medical UniversityBeijing 100069China 

出 版 物：《Journal of Traditional Chinese Medical Sciences》 (中医科学杂志（英文）)

年 卷 期：2017年第4卷第2期

页      面：174-183页

学科分类：1008[医学-中药学(可授医学、理学学位)] 1006[医学-中西医结合] 100602[医学-中西医结合临床] 10[医学] 

基　　金：The experiment was financially supported by the National Natural Science Foundation of China(81473364) Beijing Natural Science Foundation(7162122) Excellent Talents Training Subsidy Scheme of Beijing(2013D009999000003) 

主　　题：Platycodin D Biomembrane fluidity Molecular dynamics simulations Dipalmitoyl-phosphatidylcholine bilayer Transmembrane transport 

摘      要：Objective:To study the transmembrane transport of chemical components of Chinese herbs and to explore the function of platycodin D (PD) on ***:Interaction between PD and the dipalmitoylphosphatidylcholine (DPPC) bilayer was reproduced by molecular dynamics simulation with the Martini force field.A model validation and methodological study were first performed,and were based on simulation investigations of transmembrane transport for three herbal compounds with distinct hydrophilic ***:PD increased the mobility of the DPPC bilayer since its aglycone strongly interacted with the hydrophobic layer,which broke the structure of the gate layer,and weakened the ordered performance of hydrophobic ***:The Martini force field was successfully applied to the study of the interaction between herbal compounds and a biological *** combining the dynamics equilibrium morphology,the distribution of drugs inside and outside the biomembrane,and the interaction sites of drugs on the DPPC bilayer,factors influencing transmembrane transport of drugs were elucidated and the function of platycodin D in a biological membrane was reproduced.