RNA aptamers for AMPA receptors

被引:4
|
作者
Huang, Zhen [1 ]
Niu, Li [1 ]
机构
[1] SUNY Albany, Dept Chem, Ctr Neurosci Res, Albany, NY 12222 USA
基金
美国国家卫生研究院;
关键词
RNA aptamers; AMPA receptors; Kainate receptors; CNS diseases And disorders; Drug development; EXCITATORY AMINO-ACIDS; IN-VITRO SELECTION; GLUTAMATE-RECEPTOR; CRYSTAL-STRUCTURE; COMBINATORIAL CHEMISTRY; DRUG DISCOVERY; ABSOLUTE STEREOCHEMISTRY; HETEROARYL ANALOGS; PROTEIN; AGONIST;
D O I
10.1016/j.neuropharm.2021.108761
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
RNA aptamers are single-stranded RNA molecules, and they are selected against a target of interest so that they can bind to and modulate the activity of the target, such as inhibiting the target activity, with high potency and selectivity. Antagonists, such as RNA aptamers, acting on AMPA receptors, a major subtype of ionotropic glutamate receptors, are potential drug candidates for treatment of a number of CNS diseases that involve excessive receptor activation and/or elevated receptor expression. Here we review the approach to discover RNA aptamers targeting AMPA receptors from a random sequence library (similar to 10(14) sequences) through a process called systematic evolution of ligands by exponential enrichment (SELEX). As compared with small-molecule compounds, RNA aptamers are a new class of regulatory agents with interesting and desirable pharmacological properties. Some AMPA receptor aptamers we have developed are presented in this review. The promises and challenges of translating RNA aptamers into potential drugs and treatment options are also discussed.
引用
收藏
页数:11
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