Transient Induced Molecular Electronic Spectroscopy (TIMES) for study of protein-ligand interactions

被引:5
|
作者
Zhang, Tiantian [1 ]
Ku, Ti-Hsuan [2 ]
Han, Yuanyuan [2 ]
Subramanian, Ramkumar [2 ]
Niaz, Iftikhar Ahmad [2 ]
Luo, Hua [2 ,3 ]
Chang, Derrick [4 ]
Huang, Jian-Jang [5 ,6 ]
Lo, Yu-Hwa [1 ,2 ]
机构
[1] Univ Calif San Diego, Mat Sci & Engn Program, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Elect & Comp Engn, La Jolla, CA 92093 USA
[3] Sichuan Univ, Coll Basic Med & Forens Med, Coll Mfg Sci & Engn, Chengdu 610041, Sichuan, Peoples R China
[4] Univ Calif San Diego, Dept Nanoengn, La Jolla, CA 92093 USA
[5] Natl Taiwan Univ, Grad Inst Photon & Optoelect, Taipei 10617, Taiwan
[6] Natl Taiwan Univ, Dept Elect Engn, Taipei 10617, Taiwan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家科学基金会;
关键词
BINDING;
D O I
10.1038/srep35570
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We present a method, Transient Induced Molecular Electronic Spectroscopy (TIMES), to detect protein-ligand interactions without any protein engineering or chemical modification. We developed a physics model for the TIMES signal and mathematically formulated the problem to attain physical insight of protein-ligand interactions without any disturbances by molecular probes, fluorescent labels, or immobilization of molecules. To demonstrate the functionality of this method, we have used the TIMES signals to find the dissociation constants for the affinity of reactions, the shear-stress dependent adsorption time of molecules on surface, and other interesting features of protein-ligand interaction in native conditions. As a unique tool, TIMES offers a simple and effective method to investigate fundamental protein chemistry and drug discoveries.
引用
收藏
页数:8
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