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使用发光两性离子聚噻吩衍生物对DNA杂交进行芯片及溶液检测。

Chip and solution detection of DNA hybridization using a luminescent zwitterionic polythiophene derivative.

作者信息

Nilsson K Peter R, Inganäs Olle

机构信息

Biomolecular and Organic Electronics, IFM, Linköping University, SE-581 83 Linköping, Sweden.

出版信息

Nat Mater. 2003 Jun;2(6):419-24. doi: 10.1038/nmat899.

Abstract

Electronic polymers in aqueous media may offer bioelectronic detection of biospecific interactions. Here we report a fluorometric DNA hybridization detection method based on non-covalent coupling of DNA to a water-soluble zwitterionic polythiophene derivative. Introduction of a single-stranded oligonucleotide will induce a planar polymer and aggregation of the polymer chains, detected as a decrease of the intensity and a red-shift of the fluorescence. On addition of a complementary oligonucleotide, the intensity of the emitted light is increased and blue-shifted. The detection limit of this method is at present approximately 10(-11) moles. The method is highly sequence specific, and a single-nucleotide mismatch can be detected within five minutes without using any denaturation steps. The interaction with DNA and the optical phenomena persists when the polymer is deposited and patterned on a surface. This offers a novel way to create DNA chips without using covalent attachment of the receptor or labelling of the analyte.

摘要

水性介质中的电子聚合物可实现生物特异性相互作用的生物电子检测。在此,我们报告一种基于DNA与水溶性两性离子聚噻吩衍生物非共价偶联的荧光DNA杂交检测方法。引入单链寡核苷酸会诱导聚合物呈平面状并使聚合物链聚集,表现为荧光强度降低和红移。加入互补寡核苷酸后,发射光的强度增加并发生蓝移。该方法目前的检测限约为10(-11)摩尔。该方法具有高度的序列特异性,无需任何变性步骤即可在五分钟内检测出单核苷酸错配。当聚合物沉积并图案化在表面上时,其与DNA的相互作用及光学现象依然存在。这为创建DNA芯片提供了一种无需受体共价连接或分析物标记的新方法。

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