摘要
在运用量子化学从头计算方法(HF/4-31G)结合点电荷模型方法对AChE-HuPA复合物活性位点的410个原子和1929个点电荷进行理论计算的基础上,比较了石杉碱甲分子在形成复合物前后的结构变化特征.发现复合物中石杉碱甲分子构象并非能量最低构象,它的能量比HF/4-31G全优化得到的构象的能量高91.8kJ/mol.和单分子状态相比,形成复合物后季铵基和内酰胺基的N—H,C(?)O键的键长变长、键强减弱,其总原子净电荷也发生了明显的变化.且这些基团的空间取向都有不同程度的改变,C(8)—N(21)键的旋转达20°.这些信息将有益于设计新的AChE抑制剂.
The difference between Huperzine A (HupA) structure in Acetylcholinesterase (AChE) -HupA complex and the structure in gase phase has been studied by using ab initio method of quantum chemistry. The model system composed of 410 atoms abstracted from the active site of HupA - AChE complex and of the 1929 point charges around the 410 atoms was calculated employing HF/4- 31G method. The HupA itself in gase phase state was optimized with HF/4 - 31G. The calculation result indicated that the binding conformer of HupA did not adopt its lowest energy conformer. The energy difference between the binding conformer and the global minimal energy conformer of HupA is 91.8 kJ/mol. The changes of LUMO and HOMO energies indicate that the electrons were transferred between AChE and HupA. Great changes have been taken place for the total atomic charge, bond lengthes and orientations of some of the atoms and bonds in HupA when it binds to the AChE: the C= O and N-H bond of amide group and the N-H bond of the amino group of HupA have been elongated and weakened in HupA-AChE complex,the torsion angle of bond C(3)- C(8)-N(21)-H(35) alters even about 20°. These changes are caused by the hydrogen bonds formation between HupA and AChE. All of these are useful clues for designing novel huperzine A analogs to inhibite the activity of acetylcholinesterase.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
1998年第3期233-237,共5页
Acta Chimica Sinica
基金
国家自然科学基金(29403027)
"863"高科技项目基金(103-13-04-01)
