期刊
JOURNAL OF PHYSICAL CHEMISTRY B
卷 121, 期 47, 页码 10610-10617出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.7b08738
关键词
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资金
- National Natural Science Foundation of China [21376089, 21606053, 21706197, 21776093, 21706045, 91334202]
- National Key Basic Research Program of China [2013CB733500]
- Guangdong Science Foundation [2014A030312007]
- Fundamental Research Funds for the Central Universities [SCUT-2015ZP033]
Controlling the orientation of lactase on electrodes is crucial for the achievement of fast direct electron transfer. It is important to find a short pathway between the T1 copper site of lactase and a substrate during the lactase immobilization. In this work, we studied the adsorption orientation and conformation of Trametes versicolor lactase (TvL) on two kinds of charged self assembled monolayers (SAMs), including NH2 SAM and COOH SAM, by parallel tempering Monte Carlo and all-atom molecular dynamics simulations. TvL adsorbs on positively and negatively charged surface with end-on and lying orientation, respectively. On the positively charged surface, T1 copper site of TvL is closer to the surface. The orientation of TvL on positively charged surface is narrower than that on negatively charged surface. Thus, the positively charged surface is more conducive to the immobilization of TvL. The conformational changes of TvL on the charged surfaces are analyzed by RMSD, superimposed structures, dipole moment, gyration radius, and eccentricity. Results show that native structures of TvL are well preserved when it adsorbs on the charged surfaces. This work provides atomistic insight into the mechanism of TvL adsorption on charged surface and is helpful for the design and development of laccase-based electrodes.
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