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作 者:Xubo Ji Chuanguang Yao Ying Wan Hongxin Song Peng Xin Hongda Cui Chenyu Zheng Shengyuan Deng
机构地区:[1]School of Environmental and Biological and Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, China [2]School of Mechanical Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, China [3]State Key Laboratory of Analytical Chemistry for Life Science, Department of Chemistry, Nanjing University, Nanjing, Jiangsu 210093, China
出 处:《Chinese Journal of Chemistry》2016年第3期331-336,共6页中国化学(英文版)
摘 要:This work proposed a label-flee, cost-effective and fairly sensitive electrogenerated chemiluminescence (ECL) strategy for the specific detection of lysozyme based on the hemin/G-quadruplex hybrid. Gold nanoparticles were spread onto the chitosan thin-film as substrate to adsorb thiolated captures: a hairpin-structured DNA, integrating dual head-tail connected functional domains: one aptamer sequence for lysozyme and the other for hemin (iron(II1) proto-porphyrin IX). In the presence of the both, the hairpin conformation unfolded and transformed into the hemird G-quadruplex motif, which quenched the ECL emission of underlaid quantum dots significantly via the consump- tion of dissolved oxygen as endogenous coreactant. This construction enabled a wide linear response to lysozyme, ranging from 20 μg.mL-1 to 5μg. mL-1, with a detection limit as low as 4.95 pgo mL-1 (e.g. 9.4 pmol·L^-1), dem- onstrating the prospective utilization of DNA technologies in bioanalysis.This work proposed a label-flee, cost-effective and fairly sensitive electrogenerated chemiluminescence (ECL) strategy for the specific detection of lysozyme based on the hemin/G-quadruplex hybrid. Gold nanoparticles were spread onto the chitosan thin-film as substrate to adsorb thiolated captures: a hairpin-structured DNA, integrating dual head-tail connected functional domains: one aptamer sequence for lysozyme and the other for hemin (iron(II1) proto-porphyrin IX). In the presence of the both, the hairpin conformation unfolded and transformed into the hemird G-quadruplex motif, which quenched the ECL emission of underlaid quantum dots significantly via the consump- tion of dissolved oxygen as endogenous coreactant. This construction enabled a wide linear response to lysozyme, ranging from 20 μg.mL-1 to 5μg. mL-1, with a detection limit as low as 4.95 pgo mL-1 (e.g. 9.4 pmol·L^-1), dem- onstrating the prospective utilization of DNA technologies in bioanalysis.
关 键 词:APTASENSOR LYSOZYME G-QUADRUPLEX HEMIN ELECTROCHEMILUMINESCENCE
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