| 肝癌血清特异标志物Dickkopf-1核酸适体的筛选及其鉴定 |
| |
| 引用本文： | 何雷, 赵运旺, 李保林, 安晓刚. 肝癌血清特异标志物Dickkopf-1核酸适体的筛选及其鉴定[J]. 分子影像学杂志, 2019, 42(4): 528-533. doi: 10.12122/j.issn.1674-4500.2019.04.25 |
| |
| 作者姓名： | 何雷 赵运旺 李保林 安晓刚 |
| |
| 作者单位： | 1.燕山大学环境与化学工程学院，河北 秦皇岛 066004;;2.秦皇岛市第一医院，河北 秦皇岛 066000;;3.空军军医大学西京医院，陕西 西安 710032 |
| |
| 基金项目： | 国家自然科学基金（30960104；30770639）;秦皇岛市重点研发计划科技支撑项目（201902A052） |
| |
| 摘 要： | 目的筛选和鉴定肝癌血清特异标志物Dickkopf-1核酸适体(Apt)。方法采用配体指数级富集系统进化(SELEX)技术，以DKK1为靶蛋白，羧基化琼脂磁珠为筛选介质，从随机ssDNA文库中筛选出一组能够特异性与其结合的核酸适体。利用生物信息学方法对核酸适体进行序列分析和二级结构预测，表面等离子体共振仪分析测定核酸适体的亲和力。结果经过6轮消减SELEX筛选，次级ssDNA文库与DKK1靶标蛋白的亲和力趋向稳定，将第 6 轮筛选产物经PCR扩增进行高通量测序。表面等离子体共振仪检测结果表明，筛选得到的DKK1核酸适体与DKK1的结合解离常数均在纳摩尔级水平，Apt-5的Kd值最小，亲和力最高，Apt-26和Apt-28核酸适体亲和力相对较弱。二级结构预测分析表明，茎环和茎凸环结构为主要的结构形式。圆二色光谱分析结果显示，3个候选核酸适体（Apt-5, Apt-26, Apt-28）能特异形成G-四链体结构识别DKK1靶标蛋白。结论获得了与DKK1靶标蛋白特异性结合的核酸适体，为后续核酸适体的应用研究以及 DKK1蛋白功能的研究奠定了基础。
|
| 关 键 词： | Dickkopf-1 配体指数级富集系统进化技术 核酸适体 亲和力 |
| 收稿时间： | 2019-07-17 |
Screening and identification of aptamers of liver cancer serum specific marker Dickkopf-1 |
| |
| Lei HE, Yunwang ZHAO, Baolin LI, Xiaogang AN. Screening and identification of aptamers of liver cancer serum specific marker Dickkopf-1[J]. Journal of Molecular Imaging, 2019, 42(4): 528-533. doi: 10.12122/j.issn.1674-4500.2019.04.25 |
| |
| Authors: | Lei HE Yunwang ZHAO Baolin LI Xiaogang AN |
| |
| Affiliation: | 1. Department of Biological Engineering, College of Environment & Chemical Engineering, Yanshan University, Qinhuangdao 066004, China;;2. The First Hospital of Qinhuangdao, Qinhuangdao 066000, China;;3. Xijing Hospital, Air Force Medical University, Xi`an 710032,China |
| |
| Abstract: | ObjectiveTo screen and identify the serum specific marker Dickkopf-1 aptamer (Apt).MethodsThe systemic evolution of ligand by exponential enrichment (SELEX) was used to select DKK1 as the target protein and carboxylated agar magnetic beads as the screening medium. A random set of random ssDNA library was selected. A nucleic acid aptamer to which it binds. Sequence analysis and secondary structure prediction of nucleic acid aptamers were carried out by bioinformatics methods. The affinity of nucleic acid aptamers was determined by surface plasmon resonance (SPR) analysis.ResultsAfter 6 rounds of SELEX screening, the affinity of the secondary ssDNA library to the DKK1 target protein was stabilized. The 6th round of screening products were amplified by PCR for high-throughput sequencing. The results of SPR assay showed that the binding dissociation constants of DKK1 aptamers and DKK1 were in the nanomolar range. The Kd value of Apt-5 was the smallest and the affinity was the highest. The affinity of Apt-26 and Apt-28 aptamers was relative weak. The predictive analysis of secondary structure indicated that the stem loop and stem loop structure were the main structural forms. The results of circular dichroism spectroscopy showed that the three candidate aptamers (Apt-5, Apt-26, Apt-28) specifically formed the G-quadruplex structure to recognize the DKK1 target protein. Conclusion The aptamer that specifically binds to the DKK1 target protein is obtained. It laids a foundation for the application of subsequent aptamers and the study of DKK1 protein function. |
| |
| Keywords: | Dickkopf-1 SELEX technique nucleic acid aptamer affinity |
|
| 点击此处可从《分子影像学杂志》浏览原始摘要信息 |
|
点击此处可从《分子影像学杂志》下载免费的PDF全文 |
