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可待因结合RNA适体及其结合常数的直接偶联表面等离子体共振分析快速测定

Codeine-binding RNA aptamers and rapid determination of their binding constants using a direct coupling surface plasmon resonance assay.

作者信息

Win Maung Nyan, Klein Joshua S, Smolke Christina D

机构信息

Division of Chemistry and Chemical Engineering, 1200 E. California Boulevard, MC 210-41 California Institute of Technology, Pasadena, CA 91125, USA.

出版信息

Nucleic Acids Res. 2006;34(19):5670-82. doi: 10.1093/nar/gkl718. Epub 2006 Oct 11.

Abstract

RNA aptamers that bind the opium alkaloid codeine were generated using an iterative in vitro selection process. The binding properties of these aptamers, including equilibrium and kinetic rate constants, were determined through a rapid, high-throughput approach using surface plasmon resonance (SPR) analysis to measure real-time binding. The approach involves direct coupling of the target small molecule onto a sensor chip without utilization of a carrier protein. Two highest binding aptamer sequences, FC5 and FC45 with K(d) values of 2.50 and 4.00 microM, respectively, were extensively studied. Corresponding mini-aptamers for FC5 and FC45 were subsequently identified through the described direct coupling Biacore assays. These assays were also employed to confirm the proposed secondary structures of the mini-aptamers. Both aptamers exhibit high specificity to codeine over morphine, which differs from codeine by a methyl group. Finally, the direct coupling method was demonstrated to eliminate potential non-specific interactions that may be associated with indirect coupling methods in which protein linkers are commonly employed. Therefore, in addition to presenting the first RNA aptamers to a subclass of benzylisoquinoline alkaloid molecules, this work highlights a method for characterizing small molecule aptamers that is more robust, precise, rapid and high-throughput than other commonly employed techniques.

摘要

通过体外迭代筛选过程获得了能结合鸦片生物碱可待因的RNA适配体。利用表面等离子体共振(SPR)分析来测量实时结合,通过一种快速、高通量的方法确定了这些适配体的结合特性,包括平衡常数和动力学速率常数。该方法涉及将目标小分子直接偶联到传感器芯片上,而不使用载体蛋白。对两个结合能力最强的适配体序列FC5和FC45进行了深入研究,它们的解离常数(K(d))值分别为2.50和4.00 microM。随后通过所描述的直接偶联Biacore分析鉴定了FC5和FC45对应的微型适配体。这些分析还用于确认微型适配体的二级结构。两种适配体对可待因的特异性均高于吗啡,吗啡与可待因仅相差一个甲基。最后,证明直接偶联方法消除了可能与常用蛋白质连接子的间接偶联方法相关的潜在非特异性相互作用。因此,除了首次报道针对苄基异喹啉生物碱分子亚类的RNA适配体外,这项工作还突出了一种比其他常用技术更强大、精确、快速和高通量的小分子适配体表征方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f0/1636496/793a75e254c9/gkl718f1.jpg

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