ChuanMin Qi

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Name: 齐传民; Qi, ChuanMin
Organization: Beijing Normal University , China
Department:
Title: Professor(PhD)
Co-reporter:Gen He;Jie Li;Haina Ci; Chuanmin Qi; Xuefeng Guo
Angewandte Chemie International Edition 2016 Volume 55( Issue 31) pp:9036-9040
Publication Date(Web):
DOI:10.1002/anie.201603038

Abstract

Herein, we report label-free detection of single-molecule DNA hybridization dynamics with single-base resolution. By using an electronic circuit based on point-decorated silicon nanowires as electrical probes, we directly record the folding/unfolding process of individual hairpin DNAs with sufficiently high signal-to-noise ratio and bandwidth. These measurements reveal two-level current oscillations with strong temperature dependence, enabling us to determine the thermodynamic and kinetic properties of hairpin DNA hybridization. More importantly, successive, stepwise increases and decreases in device conductance at low temperature on a microsecond timescale are successfully observed, indicating a base-by-base unfolding/folding process. The process demonstrates a kinetic zipper model for DNA hybridization/dehybridization at the single base-pair level. This measurement capability promises a label-free single-molecule approach to probe biomolecular interactions with fast dynamics.

Co-reporter:Gen He;Jie Li;Haina Ci; Chuanmin Qi; Xuefeng Guo
Angewandte Chemie 2016 Volume 128( Issue 31) pp:9182-9186
Publication Date(Web):
DOI:10.1002/ange.201603038

Abstract

Herein, we report label-free detection of single-molecule DNA hybridization dynamics with single-base resolution. By using an electronic circuit based on point-decorated silicon nanowires as electrical probes, we directly record the folding/unfolding process of individual hairpin DNAs with sufficiently high signal-to-noise ratio and bandwidth. These measurements reveal two-level current oscillations with strong temperature dependence, enabling us to determine the thermodynamic and kinetic properties of hairpin DNA hybridization. More importantly, successive, stepwise increases and decreases in device conductance at low temperature on a microsecond timescale are successfully observed, indicating a base-by-base unfolding/folding process. The process demonstrates a kinetic zipper model for DNA hybridization/dehybridization at the single base-pair level. This measurement capability promises a label-free single-molecule approach to probe biomolecular interactions with fast dynamics.

Co-reporter:Yingruo Li, Hongtao Zhang, Chuanmin Qi and Xuefeng Guo  
Journal of Materials Chemistry A 2012 vol. 22(Issue 10) pp:4261-4265
Publication Date(Web):17 Nov 2011
DOI:10.1039/C1JM14872A
We demonstrate the use of P3HT–spiropyran blends as an active layer to achieve reversible photoswitching effects in solution-processed organic field-effect transistors (OFETs). Conformational changes of spiropyrans triggered by light with different wavelengths produce two distinct interaction strengths at organic/organic interfaces that can reversibly modulate the channel conductance of OFETs in a noninvasive manner. This concept of organic–organic interfacial modification offers attractive new prospects for the development of organic electronic devices with desired properties.
Co-reporter:Yingruo Li, Hongtao Zhang, Chuanmin Qi and Xuefeng Guo
Journal of Materials Chemistry A 2012 - vol. 22(Issue 10) pp:NaN4265-4265
Publication Date(Web):2011/11/17
DOI:10.1039/C1JM14872A
We demonstrate the use of P3HT–spiropyran blends as an active layer to achieve reversible photoswitching effects in solution-processed organic field-effect transistors (OFETs). Conformational changes of spiropyrans triggered by light with different wavelengths produce two distinct interaction strengths at organic/organic interfaces that can reversibly modulate the channel conductance of OFETs in a noninvasive manner. This concept of organic–organic interfacial modification offers attractive new prospects for the development of organic electronic devices with desired properties.
Pyrazolo[1,5-a]pyrimidine-3-carbonitrile, 7-chloro-5-(chloromethyl)-
Ethanol, 2-(2-hydroxyethoxy)-, 1-(4-methylbenzenesulfonate)
Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)
1,4-Benzenediamine, N,N-bis(2-chloroethyl)-
2-Chloro-N-(2-chloroethyl)-N-methylethanamine