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通过 SELEX 和高通量测序鉴定针对乳酸脱氢酶的核酸适体。

Identification of nucleic acid aptamers against lactate dehydrogenase via SELEX and high-throughput sequencing.

机构信息

Key Laboratory of Horticultural Plant Biology, Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, 430070, Hubei, China.

College of Optical and Electronic Technology, China Jiliang University, Hangzhou, 310018, Zhejiang, China.

出版信息

Anal Bioanal Chem. 2021 Jul;413(17):4427-4439. doi: 10.1007/s00216-021-03397-2. Epub 2021 May 24.

DOI:10.1007/s00216-021-03397-2
PMID:34028561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8141549/
Abstract

Nucleic acid aptamers are small fragments of DNA or RNA molecules binding specifically to targets, which can be obtained through in vitro screening via systematic evolution of ligands by exponential enrichment (SELEX). Lactate dehydrogenase (LDH) is an important tumor marker, whose level in patients is of great significance for diagnosis of many diseases. Here, we report the identification of LDH aptamers by 9 rounds of screening from a length-mixed single-stranded DNA library using the SELEX technology. After the 3rd and 7th rounds of aptamer screening, affinity was significantly improved, and fluorescence quantitative analysis showed stronger affinity for the aptamers selected from the 7th to 9th rounds of screening. After high-throughput sequencing, motif analysis, and secondary structure prediction, we finally chose and further investigated 15 candidate LDH aptamer sequences with obvious differences in secondary structure in the 7th to 9th rounds of screening. Among them, LDH7-1, LDH7-9, LDH8-2, and LDH9-1 were shown to bind to LDH protein with high affinity and specificity with K < 25 nM. This study provides new ideas for rapid detection of LDH protein content and enzyme activity, thus contributing to the development of rapid medical detection.

摘要

核酸适体是能够特异性结合靶标的 DNA 或 RNA 分子小片段,可通过指数富集配体系统进化(SELEX)的体外筛选获得。乳酸脱氢酶(LDH)是一种重要的肿瘤标志物,其在患者中的水平对许多疾病的诊断具有重要意义。在这里,我们通过 SELEX 技术从长度混合的单链 DNA 文库中经过 9 轮筛选,鉴定出了 LDH 适体。在第 3 轮和第 7 轮适体筛选后,亲和力显著提高,荧光定量分析显示,从第 7 轮到第 9 轮筛选出的适体具有更强的亲和力。经过高通量测序、基序分析和二级结构预测,我们最终选择并进一步研究了第 7 轮到第 9 轮筛选中二级结构明显不同的 15 个候选 LDH 适体序列。其中,LDH7-1、LDH7-9、LDH8-2 和 LDH9-1 与 LDH 蛋白结合具有高亲和力和特异性,Kd<25 nM。这项研究为快速检测 LDH 蛋白含量和酶活性提供了新思路,从而有助于快速医学检测的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e696/8141549/db46471035a5/216_2021_3397_Fig7_HTML.jpg
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