In this paper,the noncovalent interactions between α1-acid glycoprotein（AAG） and the drugs,such as ketoprofen（KP） and anisodine hydrobromide（AN） were studied by using electrospray ion trap mass spectrometry met...In this paper,the noncovalent interactions between α1-acid glycoprotein（AAG） and the drugs,such as ketoprofen（KP） and anisodine hydrobromide（AN） were studied by using electrospray ion trap mass spectrometry method.The results show that both of the drugs had a strong coalescent interaction with AAG,the（dissociation） constants（Kd） and the apparent stoichiometric ratio of noncovalent complexes AN-AAG were（1.75×10-3 mol/L） and 1∶7,and those for KP-AAG complex were 4.95×10-4 mol/L and 1∶4,respectively.According to the thermodynamic parameters of the noncoralent complexes,the main sorts of binding force were static-electricity gravitation for KP-AAG and Van der Waals force for AN-AAG,respectively. The experiment proves that ESI-MS technology as a new method for studying the drug-protein noncoralent binding can offer some advantages in sensitivity,speed,accuracy and directness particularly in the determination of the stoichiormetry of the complex compared to other well-established methods such as circular dichroism and fluorescence spectroscopy,etc.展开更多
文摘In this paper,the noncovalent interactions between α1-acid glycoprotein（AAG） and the drugs,such as ketoprofen（KP） and anisodine hydrobromide（AN） were studied by using electrospray ion trap mass spectrometry method.The results show that both of the drugs had a strong coalescent interaction with AAG,the（dissociation） constants（Kd） and the apparent stoichiometric ratio of noncovalent complexes AN-AAG were（1.75×10-3 mol/L） and 1∶7,and those for KP-AAG complex were 4.95×10-4 mol/L and 1∶4,respectively.According to the thermodynamic parameters of the noncoralent complexes,the main sorts of binding force were static-electricity gravitation for KP-AAG and Van der Waals force for AN-AAG,respectively. The experiment proves that ESI-MS technology as a new method for studying the drug-protein noncoralent binding can offer some advantages in sensitivity,speed,accuracy and directness particularly in the determination of the stoichiormetry of the complex compared to other well-established methods such as circular dichroism and fluorescence spectroscopy,etc.
