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竞争增强配体筛选用于球形金纳米颗粒的 DNA 适体筛选。

Competition-Enhanced Ligand Selection to Screen for DNA Aptamers for Spherical Gold Nanoparticles.

机构信息

Materials & Manufacturing Directorate, Soft Matter Materials Branch, Air Force Research Laboratory, Wright-Patterson AFB, Ohio 45433, United States.

711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, Ohio 45433, United States.

出版信息

Langmuir. 2021 Aug 3;37(30):9043-9052. doi: 10.1021/acs.langmuir.1c01053. Epub 2021 Jul 19.

Abstract

The Competition-Enhanced Ligand Selection (CompELS) approach was used to identify aptamer candidates for spherical gold nanoparticles (AuNPs). This approach differs from conventional Systematic Evolution of Ligands by EXponential enrichment (SELEX)-based aptamer screening by eliminating repeated elution and polymerase chain reaction (PCR) amplification steps of bound candidate sequences between each selection round to continually enrich the candidate aptamer pool with oligonucleotides remaining from an earlier SELEX selection round. Instead, a new pool of unenriched oligonucleotides is added during each CompELS selection round to compete with existing target-bound oligonucleotides species for target binding sites. In this study, 24 aptamer candidates for AuNPs were identified using the CompELS approach and then compared to reveal similarities in their primary structures and their predicted secondary structures. No strong patterns in individual base identities (position-dependent) nor in segments of consecutive bases (independent of position) prevailed among the identified sequences. Motifs in predicted secondary structures, on the other hand, were shared among otherwise unrelated aptamer sequences. These motifs were revealed using a systematic classification and enumeration of distinct secondary structure elements, namely, hairpins, duplexes, single-stranded segments, interior loops, bulges, and multibranched loops.

摘要

竞争增强配体选择(CompELS)方法被用于鉴定适体候选物用于球形金纳米粒子(AuNPs)。与传统的基于系统进化的配体通过指数富集(SELEX)的适体筛选方法不同,CompELS 方法消除了每个选择轮之间结合候选序列的重复洗脱和聚合酶链反应(PCR)扩增步骤,从而不断用来自早期 SELEX 选择轮的寡核苷酸来丰富候选适体库。相反,在每个 CompELS 选择轮中添加新的未富集的寡核苷酸池,与现有的靶结合寡核苷酸竞争靶结合位点。在这项研究中,使用 CompELS 方法鉴定了 24 种适体候选物用于 AuNPs,然后对其进行比较,以揭示它们的一级结构和预测的二级结构的相似之处。在鉴定的序列中,没有单个碱基身份(位置依赖)或连续碱基的片段(与位置无关)存在强烈的模式。另一方面,预测二级结构中的基序在不相关的适体序列之间共享。这些基序是通过对独特的二级结构元素(发夹、双链、单链片段、内环、凸起和多分支环)进行系统分类和枚举来揭示的。

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