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用于RNA提取和检测的三种磁珠表面功能的比较。

Comparison of three magnetic bead surface functionalities for RNA extraction and detection.

作者信息

Adams Nicholas M, Bordelon Hali, Wang Kwo-Kwang A, Albert Laura E, Wright David W, Haselton Frederick R

机构信息

†Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, United States.

‡Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States.

出版信息

ACS Appl Mater Interfaces. 2015 Mar 25;7(11):6062-9. doi: 10.1021/am506374t. Epub 2015 Mar 10.

Abstract

Magnetic beads are convenient for extracting nucleic acid biomarkers from biological samples prior to molecular detection. These beads are available with a variety of surface functionalities designed to capture particular subsets of RNA. We hypothesized that bead surface functionality affects binding kinetics, processing simplicity, and compatibility with molecular detection strategies. In this report, three magnetic bead surface chemistries designed to bind nucleic acids, silica, oligo (dT), and a specific oligonucleotide sequence were evaluated. Commercially available silica-coated and oligo (dT) beads, as well as beads functionalized with oligonucleotides complementary to respiratory syncytial virus (RSV) nucleocapsid gene, respectively recovered ∼75, ∼71, and ∼7% target RSV mRNA after a 1 min of incubation time in a surrogate patient sample spiked with the target. RSV-specific beads required much longer incubation times to recover amounts of the target comparable to the other beads (∼77% at 180 min). As expected, silica-coated beads extracted total RNA, oligo (dT) beads selectively extracted total mRNA, and RSV-specific beads selectively extracted RSV N gene mRNA. The choice of bead functionality is generally dependent on the target detection strategy. The silica-coated beads are most suitable for applications that require nucleic acids other than mRNA, especially with detection strategies that are tolerant of a high concentration of nontarget background nucleic acids, such as RT-PCR. On the other hand, oligo (dT) beads are best-suited for mRNA targets, as they bind biomarkers rapidly, have relatively high recovery, and enable detection strategies to be performed directly on the bead surface. Sequence-specific beads may be best for applications that are not tolerant of a high concentration of nontarget nucleic acids that require short RNA sequences without poly(A) tails, such as microRNAs, or that perform RNA detection directly on the bead surface.

摘要

磁珠便于在分子检测之前从生物样品中提取核酸生物标志物。这些磁珠具有多种表面功能,旨在捕获特定的RNA子集。我们假设磁珠表面功能会影响结合动力学、操作简便性以及与分子检测策略的兼容性。在本报告中,评估了三种设计用于结合核酸的磁珠表面化学性质,即二氧化硅、寡聚(dT)和特定的寡核苷酸序列。市售的二氧化硅包被磁珠和寡聚(dT)磁珠,以及用与呼吸道合胞病毒(RSV)核衣壳基因互补的寡核苷酸功能化的磁珠,在加入目标物的替代患者样品中孵育1分钟后,分别回收了约75%、约71%和约7%的目标RSV mRNA。RSV特异性磁珠需要更长的孵育时间才能回收与其他磁珠相当的目标物量(180分钟时约为77%)。正如预期的那样,二氧化硅包被磁珠提取总RNA,寡聚(dT)磁珠选择性提取总mRNA,RSV特异性磁珠选择性提取RSV N基因mRNA。磁珠功能的选择通常取决于目标检测策略。二氧化硅包被磁珠最适合需要mRNA以外核酸的应用,特别是对于耐受高浓度非目标背景核酸的检测策略,如逆转录聚合酶链反应(RT-PCR)。另一方面,寡聚(dT)磁珠最适合mRNA目标,因为它们能快速结合生物标志物,回收率相对较高,并且能直接在磁珠表面进行检测策略。序列特异性磁珠可能最适合那些不耐受高浓度非目标核酸的应用,这些应用需要没有聚(A)尾的短RNA序列,如微小RNA,或者直接在磁珠表面进行RNA检测。

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