• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于芘修饰寡核苷酸的核酸靶向探针和超分子构建的最新进展。

Recent Advances in Nucleic Acid Targeting Probes and Supramolecular Constructs Based on Pyrene-Modified Oligonucleotides.

机构信息

Institute of Chemical Biology and Fundamental Medicine SB RAS, Acad. Lavrentiev Ave. 8, Novosibirsk 630090, Russia.

出版信息

Molecules. 2017 Nov 30;22(12):2108. doi: 10.3390/molecules22122108.

DOI:10.3390/molecules22122108
PMID:29189716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6150046/
Abstract

In this review, we summarize the recent advances in the use of pyrene-modified oligonucleotides as a platform for functional nucleic acid-based constructs. Pyrene is of special interest for the development of nucleic acid-based tools due to its unique fluorescent properties (sensitivity of fluorescence to the microenvironment, ability to form excimers and exciplexes, long fluorescence lifetime, high quantum yield), ability to intercalate into the nucleic acid duplex, to act as a π-π-stacking (including anchoring) moiety, and others. These properties of pyrene have been used to construct novel sensitive fluorescent probes for the sequence-specific detection of nucleic acids and the discrimination of single nucleotide polymorphisms (SNPs), aptamer-based biosensors, agents for binding of double-stranded DNAs, and building blocks for supramolecular complexes. Special attention is paid to the influence of the design of pyrene-modified oligonucleotides on their properties, i.e., the structure-function relationships. The perspectives for the applications of pyrene-modified oligonucleotides in biomolecular studies, diagnostics, and nanotechnology are discussed.

摘要

在这篇综述中,我们总结了近年来使用芘修饰的寡核苷酸作为功能核酸基构建体平台的最新进展。由于其独特的荧光性质(荧光对微环境的敏感性、形成激基缔合物和激基复合物的能力、长荧光寿命、高量子产率)、能够嵌入核酸双链、作为π-π堆积(包括锚固)部分的能力,以及其他性质,芘特别适合开发基于核酸的工具。这些芘的性质已被用于构建新型灵敏荧光探针,用于核酸的序列特异性检测和单核苷酸多态性(SNP)的区分、基于适配体的生物传感器、双链 DNA 结合剂以及超分子复合物的构建模块。特别关注了芘修饰的寡核苷酸的设计对其性质的影响,即结构-功能关系。讨论了芘修饰的寡核苷酸在生物分子研究、诊断和纳米技术中的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0d836c027fdc/molecules-22-02108-g042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d71888f4c9ed/molecules-22-02108-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/73d07f55ba4a/molecules-22-02108-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/c48bc3ba0963/molecules-22-02108-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/92aa76a8c8f2/molecules-22-02108-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d17aab9ef507/molecules-22-02108-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8fe5fefa2d73/molecules-22-02108-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/4d3e8971b0ce/molecules-22-02108-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d860b60f2f1a/molecules-22-02108-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/5a6c51c120c7/molecules-22-02108-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/bb67b97e01f7/molecules-22-02108-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8a768c7bcba7/molecules-22-02108-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/76f7eac17fed/molecules-22-02108-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/92144e6b324e/molecules-22-02108-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/34a93e421e65/molecules-22-02108-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a257b97a88ce/molecules-22-02108-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/b2926165a9df/molecules-22-02108-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/9b95168dd89b/molecules-22-02108-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/32ff24e1690f/molecules-22-02108-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/99ccd1b6cda9/molecules-22-02108-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/dd026e644d45/molecules-22-02108-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/7d0987030be0/molecules-22-02108-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0b1f1c157483/molecules-22-02108-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8f6dc8f32dbc/molecules-22-02108-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a8da5f01b69e/molecules-22-02108-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/9359a268503c/molecules-22-02108-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/6ef65b2aaf56/molecules-22-02108-g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/f1745819b8aa/molecules-22-02108-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/6b47c2c93081/molecules-22-02108-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/114741e311a9/molecules-22-02108-g029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/91251bc46359/molecules-22-02108-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a4f60c056713/molecules-22-02108-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/18e083d59dbc/molecules-22-02108-g032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/e645f72c0ffb/molecules-22-02108-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/de964e80d6a0/molecules-22-02108-g034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0c7e58d1f024/molecules-22-02108-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d21dd063f72e/molecules-22-02108-g036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/e8fa0129e5f4/molecules-22-02108-g037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/82304ae1e5b2/molecules-22-02108-g038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/63e4f4c60bda/molecules-22-02108-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/ce692f0b9f2b/molecules-22-02108-g040.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a0f0f614d4f6/molecules-22-02108-g041.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0d836c027fdc/molecules-22-02108-g042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d71888f4c9ed/molecules-22-02108-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/73d07f55ba4a/molecules-22-02108-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/c48bc3ba0963/molecules-22-02108-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/92aa76a8c8f2/molecules-22-02108-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d17aab9ef507/molecules-22-02108-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8fe5fefa2d73/molecules-22-02108-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/4d3e8971b0ce/molecules-22-02108-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d860b60f2f1a/molecules-22-02108-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/5a6c51c120c7/molecules-22-02108-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/bb67b97e01f7/molecules-22-02108-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8a768c7bcba7/molecules-22-02108-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/76f7eac17fed/molecules-22-02108-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/92144e6b324e/molecules-22-02108-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/34a93e421e65/molecules-22-02108-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a257b97a88ce/molecules-22-02108-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/b2926165a9df/molecules-22-02108-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/9b95168dd89b/molecules-22-02108-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/32ff24e1690f/molecules-22-02108-g018.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/99ccd1b6cda9/molecules-22-02108-g019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/dd026e644d45/molecules-22-02108-g020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/7d0987030be0/molecules-22-02108-g021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0b1f1c157483/molecules-22-02108-g022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/8f6dc8f32dbc/molecules-22-02108-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a8da5f01b69e/molecules-22-02108-g024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/9359a268503c/molecules-22-02108-g025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/6ef65b2aaf56/molecules-22-02108-g026.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/f1745819b8aa/molecules-22-02108-g027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/6b47c2c93081/molecules-22-02108-g028.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/114741e311a9/molecules-22-02108-g029.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/91251bc46359/molecules-22-02108-g030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a4f60c056713/molecules-22-02108-g031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/18e083d59dbc/molecules-22-02108-g032.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/e645f72c0ffb/molecules-22-02108-g033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/de964e80d6a0/molecules-22-02108-g034.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0c7e58d1f024/molecules-22-02108-g035.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/d21dd063f72e/molecules-22-02108-g036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/e8fa0129e5f4/molecules-22-02108-g037.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/82304ae1e5b2/molecules-22-02108-g038.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/63e4f4c60bda/molecules-22-02108-g039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/ce692f0b9f2b/molecules-22-02108-g040.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/a0f0f614d4f6/molecules-22-02108-g041.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f97/6150046/0d836c027fdc/molecules-22-02108-g042.jpg

相似文献

1
Recent Advances in Nucleic Acid Targeting Probes and Supramolecular Constructs Based on Pyrene-Modified Oligonucleotides.基于芘修饰寡核苷酸的核酸靶向探针和超分子构建的最新进展。
Molecules. 2017 Nov 30;22(12):2108. doi: 10.3390/molecules22122108.
2
2'-bis-pyrene modified oligonucleotides: sensitive fluorescent probes of nucleic acids structure.2'-双芘修饰的寡核苷酸:核酸结构的灵敏荧光探针。
Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):729-34. doi: 10.1081/ncn-200060038.
3
Multilabeled pyrene-functionalized 2'-amino-LNA probes for nucleic acid detection in homogeneous fluorescence assays.用于均相荧光分析中核酸检测的多标记芘功能化2'-氨基-LNA探针。
J Am Chem Soc. 2005 Sep 28;127(38):13293-9. doi: 10.1021/ja052887a.
4
Unlocked nucleic acids with a pyrene-modified uracil: synthesis, hybridization studies, fluorescent properties and i-motif stability.带有芘修饰尿嘧啶的非锁核酸:合成、杂交研究、荧光性质和 i 型发夹结构稳定性。
Chembiochem. 2014 Jan 3;15(1):146-56. doi: 10.1002/cbic.201300567.
5
Bis-pyrene-modified unlocked nucleic acids: synthesis, hybridization studies, and fluorescent properties.双芘修饰的解锁核酸:合成、杂交研究及荧光特性
ChemMedChem. 2014 Sep;9(9):2120-7. doi: 10.1002/cmdc.201402185. Epub 2014 Jul 18.
6
Pyrene-functionalized oligonucleotides and locked nucleic acids (LNAs): tools for fundamental research, diagnostics, and nanotechnology.芘基化寡核苷酸和锁核酸 (LNA):基础研究、诊断和纳米技术的工具。
Chem Soc Rev. 2011 Dec;40(12):5771-88. doi: 10.1039/c1cs15014f. Epub 2011 Apr 13.
7
Pyrene is highly emissive when attached to the RNA duplex but not to the DNA duplex: the structural basis of this difference.芘附着于RNA双链体时具有高发射性,但附着于DNA双链体时则不然:这种差异的结构基础。
Nucleic Acids Res. 2005 Oct 19;33(18):5887-95. doi: 10.1093/nar/gki889. Print 2005.
8
A quencher-free molecular beacon design based on pyrene excimer fluorescence using pyrene-labeled UNA (unlocked nucleic acid).基于芘 excimer 荧光的无淬灭剂分子信标设计,使用芘标记的UNA(锁核酸)。
Bioorg Med Chem. 2013 Oct 15;21(20):6186-90. doi: 10.1016/j.bmc.2013.04.062. Epub 2013 May 1.
9
Highly fluorescent conjugated pyrenes in nucleic acid probes: (phenylethynyl)pyrenecarbonyl-functionalized locked nucleic acids.核酸探针中高荧光共轭芘:(苯乙炔基)芘羰基官能化的锁核酸
Chemistry. 2008;14(35):11010-26. doi: 10.1002/chem.200801077.
10
Fluorescent probes for nucleic Acid visualization in fixed and live cells.用于固定和活细胞中核酸可视化的荧光探针。
Molecules. 2013 Dec 11;18(12):15357-97. doi: 10.3390/molecules181215357.

引用本文的文献

1
Internal Dynamics of Pyrene-Labeled Polyols Studied Through the Lens of Pyrene Excimer Formation.通过芘激基缔合物形成的视角研究芘标记多元醇的内部动力学。
Polymers (Basel). 2025 Jul 18;17(14):1979. doi: 10.3390/polym17141979.
2
High performance self-assembled pyrene-based emitter with narrowband emission and excellent luminescence efficiency.具有窄带发射和优异发光效率的高性能自组装芘基发光体。
RSC Adv. 2025 Jul 21;15(32):25771-25775. doi: 10.1039/d5ra03596a.
3
Aptamer-based fluorescence biosensor for rapid detection of chloramphenicol based on pyrene excimer switch.

本文引用的文献

1
Assembly Dependent Fluorescence Enhancing Nucleic Acids in Sequence-Specific Detection of Double-Stranded DNA.用于双链DNA序列特异性检测的组装依赖性荧光增强核酸
Chempluschem. 2014 Jan;79(1):58-66. doi: 10.1002/cplu.201300310. Epub 2013 Dec 2.
2
25 years and still going strong: 2'-O-(pyren-1-yl)methylribonucleotides - versatile building blocks for applications in molecular biology, diagnostics and materials science.25年依然强劲:2'-O-(芘-1-基)甲基核糖核苷酸——分子生物学、诊断学和材料科学应用中的多功能构建模块。
Org Biomol Chem. 2017 Nov 29;15(46):9760-9774. doi: 10.1039/c7ob02152f.
3
Studying the influence of stem composition in pH-sensitive molecular beacons onto their sensing properties.
基于芘激基缔合物开关的适体荧光生物传感器用于快速检测氯霉素
Anal Bioanal Chem. 2025 Mar;417(8):1441-1448. doi: 10.1007/s00216-025-05733-2. Epub 2025 Jan 20.
4
Exploring Imaging Applications of a Red-Emitting π-Acceptor (π-A) Pyrene-Benzothiazolium Dye.探索一种发红光的π受体(π-A)芘-苯并噻唑鎓染料的成像应用。
Biosensors (Basel). 2024 Dec 13;14(12):612. doi: 10.3390/bios14120612.
5
Photoionization of pyrenemethylamine-labeled oligosaccharides: a new MALDI-TOF precursor ion-type for efficient fragmentation.芘甲胺标记的寡糖的光离子化:一种用于高效裂解的新型基质辅助激光解吸电离飞行时间前体离子类型。
Anal Sci. 2025 Mar;41(3):297-310. doi: 10.1007/s44211-024-00700-w. Epub 2024 Dec 10.
6
Enhanced Sequence-Specific DNA Recognition Using Oligodeoxynucleotide-Benzimidazole Conjugates.使用寡脱氧核苷酸-苯并咪唑缀合物增强序列特异性DNA识别
ACS Bio Med Chem Au. 2024 Apr 16;4(3):154-164. doi: 10.1021/acsbiomedchemau.3c00074. eCollection 2024 Jun 19.
7
Pursuing excitonic energy transfer with programmable DNA-based optical breadboards.采用可编程 DNA 光学实验平台实现激子能量转移。
Chem Soc Rev. 2023 Nov 13;52(22):7848-7948. doi: 10.1039/d0cs00936a.
8
Gated Photoreactivity of Pyrene Copolymers in Multiresponsive Cross-Linked starPEG-Hydrogels.芘共聚物在多响应交联星形聚乙二醇水凝胶中的门控光反应性
ACS Polym Au. 2021 Jul 12;1(1):59-66. doi: 10.1021/acspolymersau.1c00011. eCollection 2021 Aug 11.
9
Dynamically stable and amplified circularly polarized excimer emission regulated by solvation of chiral co-assembly process.通过手性共组装过程的溶剂化作用调控的动态稳定且放大的圆偏振准分子发射。
Nat Commun. 2022 Aug 20;13(1):4905. doi: 10.1038/s41467-022-32714-1.
10
study on the excited states of pyrene and its derivatives using multi-reference perturbation theory methods.使用多参考扰动理论方法对芘及其衍生物的激发态进行研究。
RSC Adv. 2020 Mar 31;10(22):12988-12998. doi: 10.1039/c9ra10483f. eCollection 2020 Mar 30.
研究茎组成对 pH 敏感分子信标的传感性能的影响。
Anal Chim Acta. 2017 Oct 16;990:157-167. doi: 10.1016/j.aca.2017.07.040. Epub 2017 Jul 21.
4
Automated Solid-Phase Click Synthesis of Oligonucleotide Conjugates: From Small Molecules to Diverse N-Acetylgalactosamine Clusters.寡核苷酸缀合物的自动化固相点击合成:从小分子到多样的N-乙酰半乳糖胺簇
Bioconjug Chem. 2017 Oct 18;28(10):2599-2607. doi: 10.1021/acs.bioconjchem.7b00462. Epub 2017 Oct 4.
5
LNA effects on DNA binding and conformation: from single strand to duplex and triplex structures.LNA 对 DNA 结合和构象的影响:从单链到双链和三链结构。
Sci Rep. 2017 Sep 8;7(1):11043. doi: 10.1038/s41598-017-09147-8.
6
Fine Tuning of Pyrene Excimer Fluorescence in Molecular Beacons by Alteration of the Monomer Structure.通过改变单体结构对芘激基复合物荧光的精调。
J Org Chem. 2017 Oct 6;82(19):10015-10024. doi: 10.1021/acs.joc.7b01451. Epub 2017 Sep 14.
7
Spectroscopic study of fluorescent probes based on G-quadruplex oligonucleotides labeled with ethynylpyrenyldeoxyuridine.基于乙炔基芘基脱氧尿苷标记的 G-四链体寡核苷酸的荧光探针的光谱研究。
Int J Biol Macromol. 2017 Dec;105(Pt 1):862-872. doi: 10.1016/j.ijbiomac.2017.07.107. Epub 2017 Jul 17.
8
CRISPR/Cas9-Based Genome Editing for Disease Modeling and Therapy: Challenges and Opportunities for Nonviral Delivery.基于 CRISPR/Cas9 的基因组编辑在疾病建模和治疗中的应用:非病毒递送的挑战和机遇。
Chem Rev. 2017 Aug 9;117(15):9874-9906. doi: 10.1021/acs.chemrev.6b00799. Epub 2017 Jun 22.
9
Hybridization chain reaction: a versatile molecular tool for biosensing, bioimaging, and biomedicine.杂交链式反应:一种用于生物传感、生物成像和生物医学的多功能分子工具。
Chem Soc Rev. 2017 Jul 17;46(14):4281-4298. doi: 10.1039/c7cs00055c.
10
Aggregate Formation of Oligonucleotides that Assist Molecular Imaging for Tracking of the Oxygen Status in Tumor Tissue.辅助分子成像以跟踪肿瘤组织氧状态的寡核苷酸聚集体形成
Chembiochem. 2017 Aug 17;18(16):1650-1658. doi: 10.1002/cbic.201700116. Epub 2017 Jun 28.