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通过呋喃氧化进行的三链交联需要对结构化三链螺旋进行扰动。

Triplex crosslinking through furan oxidation requires perturbation of the structured triple-helix.

作者信息

Gyssels Ellen, Carrette Lieselot L G, Vercruysse Emma, Stevens Kristof, Madder Annemieke

机构信息

Organic and Biomimetic Chemistry Research Group, Department of Organic and Macromolecular Chemistry, Ghent University, Krijgslaan 281, S4, 9000 Gent (Belgium).

出版信息

Chembiochem. 2015 Mar 2;16(4):651-8. doi: 10.1002/cbic.201402602. Epub 2015 Jan 28.

Abstract

Short oligonucleotides can selectively recognize duplexes by binding in the major groove thereby forming triplexes. Based on the success of our recently developed strategy for furan-based crosslinking in DNA duplexes, we here investigated for the first time the use of the furan-oxidation crosslink methodology for the covalent locking of triplex structures by an interstrand crosslink. It was shown that in a triplex context, although crosslinking yields are surprisingly low (to nonexistent) when targeting fully complementary duplexes, selective crosslinking can be achieved towards mismatched duplex sites at the interface of triplex to duplex structures. We show the promising potential of furan-containing probes for the selective detection of single-stranded regions within nucleic acids containing a variety of structural motifs.

摘要

短寡核苷酸可通过在大沟中结合从而形成三链体来选择性识别双链体。基于我们最近开发的用于DNA双链体中基于呋喃的交联策略的成功,我们在此首次研究了使用呋喃氧化交联方法通过链间交联对三链体结构进行共价锁定。结果表明,在三链体环境中,尽管靶向完全互补的双链体时交联产率出奇地低(甚至不存在),但对于三链体与双链体结构界面处的错配双链体位点可实现选择性交联。我们展示了含呋喃探针在选择性检测含有多种结构基序的核酸内单链区域方面的广阔潜力。

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