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一对部分非互补的肽核酸对双链DNA中错配位点的识别

Recognition of mismatched sites in double-stranded DNA by a pair of partially noncomplementary peptide nucleic acids.

作者信息

Shibata Masanari, Shoji Osami, Aiba Yuichiro

机构信息

Department of Chemistry, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8602, Japan.

出版信息

Chem Lett. 2024 Dec 10;53(12):upae234. doi: 10.1093/chemle/upae234. eCollection 2024 Dec.

DOI:10.1093/chemle/upae234
PMID:39677325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11640769/
Abstract

We have successfully achieved efficient recognition of mismatched sites in double-stranded DNA through the formation of an invasion complex by using partially noncomplementary peptide nucleic acids (PNAs). Owing to mismatches between 2 PNAs used for invasion, the undesired PNA/PNA duplex, which inhibits invasion complex formation, was destabilized. This approach overcame an inherent challenge in PNA invasion, in particular, undesired PNA/PNA duplex formation resulting from PNA complementarity, thereby enhancing overall invasion efficiency.

摘要

我们通过使用部分非互补肽核酸(PNA)形成入侵复合物,成功实现了对双链DNA中错配位点的高效识别。由于用于入侵的两个PNA之间存在错配,抑制入侵复合物形成的不期望的PNA/PNA双链体变得不稳定。这种方法克服了PNA入侵中固有的挑战,特别是由PNA互补性导致的不期望的PNA/PNA双链体形成,从而提高了整体入侵效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/e2a57db5a439/upae234f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/f2055449250f/upae234_ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/68a8e267628b/upae234f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/14d8da921f2f/upae234f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/5e16929c578d/upae234f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/e2a57db5a439/upae234f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/f2055449250f/upae234_ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/68a8e267628b/upae234f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/14d8da921f2f/upae234f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/5e16929c578d/upae234f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed5/11640769/e2a57db5a439/upae234f4.jpg

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本文引用的文献

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Recent Advancements in Development and Therapeutic Applications of Genome-Targeting Triplex-Forming Oligonucleotides and Peptide Nucleic Acids.基因组靶向三链形成寡核苷酸和肽核酸的开发及治疗应用的最新进展
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Unique Crosslinking Properties of Psoralen-Conjugated Oligonucleotides Developed by Novel Psoralen N-Hydroxysuccinimide Esters.新型补骨脂素N-羟基琥珀酰亚胺酯开发的补骨脂素共轭寡核苷酸的独特交联特性。
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Pseudo-Complementary G:C Base Pair for Mixed Sequence dsDNA Invasion and Its Applications in Diagnostics (SARS-CoV-2 Detection).用于混合序列双链DNA侵入的伪互补G:C碱基对及其在诊断中的应用(严重急性呼吸综合征冠状病毒2检测)
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In vivo correction of cystic fibrosis mediated by PNA nanoparticles.肽核酸纳米颗粒介导的囊性纤维化体内校正。
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