适体
指数富集配体系统进化
表位
凝血酶
SELEX适体技术
选择(遗传算法)
计算生物学
化学
生物
重组DNA
抗体
DNA
单克隆抗体
分子生物学
生物化学
遗传学
计算机科学
基因
核糖核酸
免疫学
人工智能
血小板
作者
Robert Wilson,Andrew R. Cossins,Dan V. Nicolau,Sotiris Missailidis
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert]
日期:2013-02-01
卷期号:23 (1): 88-92
被引量:11
标识
DOI:10.1089/nat.2012.0386
摘要
Nearly all aptamers identified so far for any given target molecule have been specific for the same binding site (epitope). The most notable exception to the 1 aptamer per target molecule rule is the pair of DNA aptamers that bind to different epitopes of thrombin. This communication refutes the suggestion that these aptamers exist because different partitioning methods were used when they were selected. The possibility that selection of these aptamers was biased by conflicting secondary structures was also investigated and found not to contribute. The preparation of protein-coated magnetic beads for systematic evolution of ligands by exponential enrichment (SELEX) and the different specificities of the thrombin aptamers for the α and β forms of thrombin are also reported.
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