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寡核苷酸中 P3'→N5' 膦酸酰胺键的断裂由单链寡核苷酸模板介导。

Cleavage of oligonucleotides containing a P3'→N5' phosphoramidate linkage mediated by single-stranded oligonucleotide templates.

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Molecules. 2011 Dec 20;16(12):10695-708. doi: 10.3390/molecules161210695.

DOI:10.3390/molecules161210695
PMID:22186956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6264227/
Abstract

Double-stranded DNA (dsDNA) templates can hybridize to and accelerate cleavage of oligonucleotides containing a P3'→N5' phosphoramidate (P-N) linkage. This dsDNA-templated cleavage of P-N linkages could be due to conformational strain placed on the linkage upon triplex formation. To determine whether duplex formation also induced conformational strain, we examined the reactivity of the oligonucleotides with a P-N linkage in the presence of single-stranded templates, and compared these reactions to those with dsDNA templates. P-N oligonucleotides that are cleaved upon duplex formation could be used as probes to detect single-stranded nucleic acids.

摘要

双链 DNA (dsDNA) 模板可以杂交并加速含有 P3'→N5' 膦酰胺酸酯 (P-N) 键的寡核苷酸的切割。这种 dsDNA 模板切割 P-N 键可能是由于三链体形成时在键上产生的构象应变。为了确定双链体形成是否也会引起构象应变,我们研究了在单链模板存在下具有 P-N 键的寡核苷酸的反应性,并将这些反应与具有 dsDNA 模板的反应进行了比较。在双链体形成时被切割的 P-N 寡核苷酸可用作探针来检测单链核酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/b007494292a8/molecules-16-10695-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/eb89b810f2ad/molecules-16-10695-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/68817d89e2fe/molecules-16-10695-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/28a9e21d6fae/molecules-16-10695-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/a8a314410614/molecules-16-10695-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/eade6010990b/molecules-16-10695-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/b196ea221975/molecules-16-10695-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/b007494292a8/molecules-16-10695-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/eb89b810f2ad/molecules-16-10695-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/68817d89e2fe/molecules-16-10695-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/28a9e21d6fae/molecules-16-10695-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/a8a314410614/molecules-16-10695-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/eade6010990b/molecules-16-10695-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/b196ea221975/molecules-16-10695-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907e/6264227/b007494292a8/molecules-16-10695-g006.jpg

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Biochemistry. 2011 Aug 30;50(34):7414-25. doi: 10.1021/bi200477g. Epub 2011 Aug 8.
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A fluorogenic reaction based on heavy-atom removal for ultrasensitive DNA detection.基于重原子去除的荧光反应用于超灵敏 DNA 检测。
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Double-stranded DNA-templated cleavage of oligonucleotides containing a P3'->N5' linkage triggered by triplex formation: the effects of chemical modifications and remarkable enhancement in reactivity.
双链 DNA 模板引导的寡核苷酸断裂,其中包含 P3'->N5' 键,由三链体形成触发:化学修饰的影响和反应性的显著增强。
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