Department of Agriculture, University of Zanjan, Zanjan, Iran; Research and Development Department, Nanozino, Tehran, Iran.
Research and Development Department, Nanozino, Tehran, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2019 Apr 5;212:173-179. doi: 10.1016/j.saa.2018.12.050. Epub 2018 Dec 29.
Infectious bursal disease virus is a causative agent of one of the most important disease which causes frequent tragic disaster in the poultry industry all over the world. Therefore, in the present study a new fluorescence resonance energy transfer-based technique was developed to detect VP2 gene of infectious bursal disease virus using two oligonucleotide probes labeled with quantum dots and rhodamine- immobilized gold nanoparticles (AuNPs-Rh). Quantum dots labeled with an amino-modified first oligonucleotide, and AuNPs-Rh labeled with thiol-modified second oligonucleotides were added to the DNA targets upon which hybridization occurred. In the presence of target the AuNPs-Rh will be located in the vicinity of the quantum dots and leads to the fluorescence resonance energy transfer to be occurred and subsequently the fluorescence intensity of quantum dots was stimulated. The immobilization of rhodamine to the surface of AuNPs increased the fluorescence intensity of rhodamine. The maximum fluorescence resonance energy transfer efficiency for the developed sensor is monitored at a quantum dots-P/AuNPs-Rh-P molar ratio of 1:10. Moreover, the feasibility of the developed nanobiosensor was demonstrated by the detection of a synthetic 49-mer nucleotide derived from infectious bursal disease virus and the limit of detection was estimated as 3 × 10 M. The developed DNA detection scheme is a simple, rapid and efficient technique which does not need excessive washing and separation steps.
传染性法氏囊病病毒是一种病原体,是导致全球家禽业频繁发生重大灾难的最重要疾病之一。因此,在本研究中,开发了一种新的基于荧光共振能量转移的技术,使用两种寡核苷酸探针标记量子点和固定在金纳米粒子(AuNPs-Rh)上的罗丹明来检测传染性法氏囊病病毒的 VP2 基因。标记有氨基修饰的第一寡核苷酸的量子点,和标记有巯基修饰的第二寡核苷酸的 AuNPs-Rh 被添加到 DNA 靶标上,从而发生杂交。在存在靶标的情况下,AuNPs-Rh 将位于量子点附近,导致荧光共振能量转移发生,随后量子点的荧光强度被激发。罗丹明固定在 AuNPs 的表面增加了罗丹明的荧光强度。开发的传感器的最大荧光共振能量转移效率在量子点-P/AuNPs-Rh-P 摩尔比为 1:10 时监测到。此外,通过检测来自传染性法氏囊病病毒的合成 49 核苷酸证明了开发的纳米生物传感器的可行性,检测限估计为 3×10-7 M。所开发的 DNA 检测方案是一种简单、快速、高效的技术,不需要过多的洗涤和分离步骤。