Du Ting-E, Wang Yiyun, Zhang Yi, Zhang Tian, Mao Xun
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, Shaanxi Province 710127, PR China.
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, Shaanxi Province 710127, PR China.
Anal Chim Acta. 2015 Feb 25;861:69-73. doi: 10.1016/j.aca.2014.12.044. Epub 2014 Dec 27.
We used cotton thread as substrate to develop a novel room temperature DNA detection device for low-cost, sensitive and rapid detection of a human genetic disease, hereditary tyrosinemia type I related DNA sequences. A novel adenosine based molecular beacon (ABMB) probe modified on gold nanoparticle was used as reporter probe. In the presence of coralyne, a small molecule which can react with adenosines, the ABMB would form a hairpin structure just like traditional molecular beacon used extensively. In the presence of target DNA sequences, the hairpin structure of ABMB modified on gold nanoparticles will be opened and the biotin group modified at one end of the DNA probes will be released and react with the streptavidin immobilized on the test zone of the cotton thread. The response of the thread based DNA test device is linear over the range of 2.5-100 nM complementary DNA. The ability of our developed device for discriminating the single base mismatched DNA related to a human genetic disease, hereditary tyrosinemia type I, was improved comparing with previous report. It is worth mentioning that the whole assay procedure for DNA test is performed under room temperature which simplified the assay procedures greatly.
我们使用棉线作为底物,开发了一种新型的室温DNA检测装置,用于低成本、灵敏且快速地检测一种人类遗传疾病——I型遗传性酪氨酸血症相关的DNA序列。一种修饰在金纳米颗粒上的新型基于腺苷的分子信标(ABMB)探针被用作报告探针。在可与腺苷发生反应的小分子珊瑚灵存在的情况下,ABMB会像广泛使用的传统分子信标一样形成发夹结构。在存在目标DNA序列时,修饰在金纳米颗粒上的ABMB的发夹结构将被打开,DNA探针一端修饰的生物素基团将被释放,并与固定在棉线检测区的链霉亲和素发生反应。基于棉线的DNA检测装置的响应在2.5 - 100 nM互补DNA范围内呈线性。与之前的报道相比,我们开发的装置区分与人类遗传疾病I型遗传性酪氨酸血症相关的单碱基错配DNA的能力有所提高。值得一提的是,DNA检测的整个分析过程在室温下进行,这极大地简化了分析程序。