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[通过指数富集的配体系统进化技术对炭疽芽孢杆菌孢子适配体的体外筛选及亲和力功能研究]

[In vitro selection and affinity function of the aptamers to Bacillus anthracis spores by SELEX].

作者信息

Zhen Bei, Song Ya-Jun, Guo Zhao-Biao, Wang Jin, Zhang Min-Li, Yu Shou-Yi, Yang Rui-Fu

机构信息

Institute of Microbiology and Epidemiology, the Academy of Military Medical Sciences, Beijing 100071, China.

出版信息

Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2002 Sep;34(5):635-42.

Abstract

To obtain oligonucleotide aptamers, specifically binding to Bacillus anthracis spores, and to find the relationship between the structures and the affinities, and to determine whether the aptamers can be used as a novel molecule for spore detection, a synthetic 35 mer random DNA library was subjected to 18 rounds of selection by using SELEX (systematic evolution of ligands by exponential enrichment) protocol against spores of Bacillus anthracis vaccine strain A. 16R. The selected aptamers were cloned and sequenced. Software packages CLUSTALX (1.8) and DNASIS v2.5 were employed to analyze the conserved sequences and second structures of the aptamers, respectively. Affinities of aptamers to the spores were visualized by biotin streptavidin horseradish peroxidase system. DAB was used to visualize signals, as an assay method. A membrane-based hybrid sandwich assay was developed for detecting Bacillus anthracic spores by using a 5'-biotinylated ssDNA aptamers and anti-spore antibodies. PCR amplification band pattern of the first round selection was different from that of the ninth round. The binding assay demonstrated that the affinity of the eighteenth round pool increased thirty-seven folds more than that of the first round pool. The affinities of the aptamers were different: the highest A at 450 nm was 1.20, and the lowest was 0.20. The secondary structure analysis revealed possible stem-loop and hairpin structures for binding to the spores. The colorimetry on the immuno-membrane got the best signal with a ratio of 16 microgram aptamer to 4x10(7) spores. A set of aptamers with considerable binding affinity to Bacillus anthracis spores was successfully selected from the initial random ssDNA pool. The stem-loop and hairpin at 5' end of the aptamers worked as the main motif in the interaction between oligonucleotides and spores, while the neighbor bases of the triple structure might affect the stability. Therefore ssDNA aptamers seem to be a type of potential diagnostic molecule.

摘要

为获得能特异性结合炭疽芽孢杆菌孢子的寡核苷酸适配体,找出其结构与亲和力之间的关系,并确定这些适配体是否可作为一种用于孢子检测的新型分子,使用指数富集配体系统进化技术(SELEX),针对炭疽芽孢杆菌疫苗株A. 16R的孢子,对一个合成的35聚体随机DNA文库进行了18轮筛选。对筛选出的适配体进行克隆和测序。分别使用CLUSTALX(1.8)和DNASIS v2.5软件包分析适配体的保守序列和二级结构。通过生物素 - 链霉亲和素 - 辣根过氧化物酶系统观察适配体与孢子的亲和力。采用二氨基联苯胺(DAB)显色作为检测方法。利用5'-生物素化的单链DNA适配体和抗孢子抗体开发了一种基于膜的杂交夹心检测法,用于检测炭疽芽孢杆菌孢子。第一轮筛选的PCR扩增条带模式与第九轮不同。结合试验表明,第十八轮混合文库的亲和力比第一轮混合文库增加了37倍。不同适配体的亲和力不同:450nm处最高吸光度A为1.20,最低为0.20。二级结构分析揭示了可能存在的茎环和发夹结构,用于与孢子结合。免疫膜比色法在适配体与孢子比例为16微克适配体比4×10⁷个孢子时获得最佳信号。从初始随机单链DNA文库中成功筛选出一组对炭疽芽孢杆菌孢子具有相当结合亲和力的适配体。适配体5'端的茎环和发夹结构是寡核苷酸与孢子相互作用的主要基序,而三重结构的相邻碱基可能影响稳定性。因此,单链DNA适配体似乎是一种潜在的诊断分子。

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