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利用茎环DNA信标检测RNA中的无碱基位点:应用于蓖麻毒素A链活性测定

Detection of an abasic site in RNA with stem-loop DNA beacons: application to an activity assay for Ricin Toxin A-Chain.

作者信息

Roday Setu, Sturm Matthew B, Blakaj Dukajgin, Schramm Vern L

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, United States.

出版信息

J Biochem Biophys Methods. 2008 Apr 24;70(6):945-53. doi: 10.1016/j.jprot.2007.12.010. Epub 2008 Jan 16.

DOI:10.1016/j.jprot.2007.12.010
PMID:18276012
Abstract

The catalytic ability of Ricin Toxin A-Chain (RTA) to create an abasic site in a 14-mer stem-tetraloop RNA is exploited for its detection. RTA catalyzes the hydrolysis of the N-glycosidic bond of a specific adenosine in the GAGA tetraloop of stem-loop RNA. Thus, a 14-mer stem-loop RNA substrate containing an intact "GAGA" sequence can be discriminated from the product containing an abasic "GabGA" sequence by hybridization with a 14-mer DNA stem-loop probe sequence and following the fluorescent response of the heteroduplexes. Three DNA beacon probe designs are described. Beacon 1 probe is a stem-loop structure and has a fluorophore and a quencher covalently linked to the 5'- and 3'-ends. In this format the probe-substrate heteroduplex gives a fluorescent signal while the probe-product one remains quenched. Beacon 2 is a modified version of 1 and incorporates a pyrene deoxynucleoside for recognition of the abasic site. In this format both the substrate and product heteroduplexes give a fluorescent response. Beacon 3 utilizes a design where the fluorophore is on the substrate RNA sequence at its 5'-end while the quencher is on the probe DNA sequence at its 3'-end. In this format the fluorescence of the substrate-probe heteroduplex is quenched while that of the product-probe one is enhanced. The lower limit of detection with beacons is 14 ng/mL of RTA.

摘要

利用蓖麻毒素A链(RTA)在14聚体茎四环RNA中产生无碱基位点的催化能力来进行检测。RTA催化茎环RNA的GAGA四环中特定腺苷的N-糖苷键水解。因此,通过与14聚体DNA茎环探针序列杂交并跟踪异源双链体的荧光响应,可以将含有完整“GAGA”序列的14聚体茎环RNA底物与含有无碱基“GabGA”序列的产物区分开来。描述了三种DNA信标探针设计。信标1探针是一种茎环结构,在5'端和3'端共价连接有荧光团和猝灭剂。在这种形式下,探针-底物异源双链体产生荧光信号,而探针-产物异源双链体保持猝灭状态。信标2是信标1的改进版本,并入了一个芘脱氧核苷用于识别无碱基位点。在这种形式下,底物和产物异源双链体都产生荧光响应。信标3采用的设计是荧光团位于底物RNA序列的5'端,而猝灭剂位于探针DNA序列的3'端。在这种形式下,底物-探针异源双链体的荧光被猝灭,而产物-探针异源双链体的荧光增强。信标检测RTA的下限为14 ng/mL。

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