Structure-dependent electrical conductivity of protein: its differences between alphadomain and beta-domain structures
Structure-dependent electrical conductivity of protein: its differences between alphadomain and beta-domain structures
复制标题
蛋白质的结构依赖性电导率:α结构域和β结构域结构之间的差异
DOI:
10.1088/0957-4484/26/12/125702
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发表时间:
2015
期刊:
影响因子:
3.5
通讯作者:
Yue Zheng
中科院分区:
文献类型:
--
作者:
X. Y. Zhang;J. Shao;S. X. Jiang;B. Wang;Yue Zheng
Electron transports in the α-domain and β-domain of proteins have been comprehensively investigated. The structure-dependent electron transport of proteins has been experimentally measured and theoretically simulated, and both the theoretical and experimental results demonstrate significant differences in electrical conductivity between the α-domain and β-domain. By controlling the feedback system of the scanning tunneling microscope (STM), the conductance of a single α-domain protein hemoglobin (Hgb) and a β-domain protein superoxide dismutase enzyme (SOD) were measured, respectively. The current signal of Hgb is obviously stronger, indicating that the α-domain is more conductive. To confirm our finding, molecular orbitals of both the β-domain in SOD and α-domain in Hgb have been analyzed based on first-principles calculations. As expected, tunneling transport and hopping in the α-domain are both more efficient, indicating that it is easier for electrons to transport through the α-domain, which are in great agreement with our experimental data. In order to explain our results, molecular structures of α-and β-domains have been carefully analyzed and show that the explanation should lie in the differences in packing mode between the α-domain and β-domain. This research should be very important to application prospects in molecular electronics.