首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Photoelectrochemical biosensor of HIV-1 based on cascaded photoactive materials and triple-helix molecular switch
【24h】

Photoelectrochemical biosensor of HIV-1 based on cascaded photoactive materials and triple-helix molecular switch

机译:基于级联光活性材料和三螺旋分子开关的HIV-1光电化学生物传感器

获取原文
获取原文并翻译 | 示例
           

摘要

In this work, an ultrasensitive photoelectrochemical (PEC) biosensor was proposed to detect nucleic acids on the basis of cascaded photoactive materials and triple-helix molecular switch. DNA sequence of human immunodeficiency virus type 1 (HIV-1) was chosen as the target DNA (T-DNA). Cascaded photoactive structure was formed via different sizes of CdTe quantum dots (QDs) sensitized ZnO nanorods (ZnO NRs), which was employed as a cascaded photoactive interface to amplify the photocurrent signal. A hairpin structure DNA (H-DNA) as capture probe was conjugated onto the photoactive interface through amide bond, and then a single-stranded DNA modified with gold nanoparticles labeled alkaline phosphatase (ALP-Au NPs-DNA) at each end was introduced to hybridize with the H-DNA to form a triple-helix conformation. The T-DNA detection was based on the photocurrent response change resulted from conformation change of the triple-helix molecule after hybridization with T-DNA. In the absence of T-DNA, the triple-helix molecule was in a closed state and the ALP of ALP-Au NPs-DNA could specifically catalyze the ascorbic acid 2-phosphate (AAP) to generate ascorbic acid (AA) as electron donors, which resulted in a significant photocurrent response due to the rapid electron transfer process. However, in the presence of T-DNA, the T-DNA hybridized with the ALP-Au NPs-DNA molecule, which caused triple-helix molecule in an opened state and compelled ALP-Au NPs-DNA away from the electrode surface, resulting in the absence of ALP which could catalyze AAP to generate AA. Subsequently, the photocurrent response significantly decreased. The proposed PEC biosensor not only had a wide detection range of 1fM-1nM and low detection limit (0.65 fM), but also showed excellent reproducibility, specificity and stability, which had great application prospect and opened up a new research method in the early clinical diagnosis and cancer research.
机译:在这项工作中,提出了超敏感的光电化学(PEC)生物传感器在级联光活性材料和三螺旋分子开关的基础上检测核酸。选择人免疫缺陷病毒类型1(HIV-1)的DNA序列作为靶DNA(T-DNA)。通过不同尺寸的CDTE量子点(QDS)敏化ZnO纳米棒(ZnO NRS)形成级联光活性结构,其用作级联的光活性界面以扩增光电流信号。作为捕获探针的发夹结构DNA(H-DNA)通过酰胺键在光活性界面上缀合,然后引入每端的金纳米颗粒标记的金纳米粒子标记的碱性磷酸酶(ALP-AU NPS-DNA)进行了一种单链DNA。用H-DNA杂交以形成三螺旋构象。 T-DNA检测基于与T-DNA杂交后的三螺旋分子的构象变化导致的光电流响应变化。在没有T-DNA的情况下,三螺旋分子处于闭合状态,ALP-Au NPS-DNA的ALP可以特异性地催化抗坏血酸2-磷酸(AAP)以产生抗坏血酸(AA)作为电子供体,由于电子转移过程的快速,导致显着的光电流响应。然而,在T-DNA存在下,与ALP-AU NPS-DNA分子杂交的T-DNA,其在打开状态下引起三螺旋分子并将AlP-Au NPS-DNA电压从电极表面上缩短,得到在没有ALP的情况下,可以催化AAP产生AA。随后,光电流响应显着降低。所提出的PEC生物传感器不仅具有宽的1FM-1nm和低检测限(0.65 fm)的宽检测范围,而且还显示出优异的再现性,特异性和稳定性,具有很大的应用前景并在早期临床中开辟了一种新的研究方法诊断和癌症研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号