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4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics

Unnatural nucleosides possessing unique spectroscopic properties that mimic natural nucleobases in both size and chemical structure are ideally suited for spectroscopic measurements of DNA/RNA structure and dynamics in a site-specific manner. However, such unnatural nucleosides are scarce, which pro...

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Autores principales: Ahmed, Ismail A., Acharyya, Arusha, Eng, Christina M., Rodgers, Jeffrey M., DeGrado, William F., Jo, Hyunil, Gai, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384856/
https://www.ncbi.nlm.nih.gov/pubmed/30744004
http://dx.doi.org/10.3390/molecules24030602
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author Ahmed, Ismail A.
Acharyya, Arusha
Eng, Christina M.
Rodgers, Jeffrey M.
DeGrado, William F.
Jo, Hyunil
Gai, Feng
author_facet Ahmed, Ismail A.
Acharyya, Arusha
Eng, Christina M.
Rodgers, Jeffrey M.
DeGrado, William F.
Jo, Hyunil
Gai, Feng
author_sort Ahmed, Ismail A.
collection PubMed
description Unnatural nucleosides possessing unique spectroscopic properties that mimic natural nucleobases in both size and chemical structure are ideally suited for spectroscopic measurements of DNA/RNA structure and dynamics in a site-specific manner. However, such unnatural nucleosides are scarce, which prompts us to explore the utility of a recently found unnatural nucleoside, 4-cyanoindole-2′-deoxyribonucleoside (4CNI-NS), as a site-specific spectroscopic probe of DNA. A recent study revealed that 4CNI-NS is a universal nucleobase that maintains the high fluorescence quantum yield of 4-cyanoindole and that among the four natural nucleobases, only guanine can significantly quench its fluorescence. Herein, we further show that the C≡N stretching frequency of 4CNI-NS is sensitive to the local environment, making it a useful site-specific infrared probe of oligonucleotides. In addition, we demonstrate that the fluorescence-quencher pair formed by 4CNI-NS and guanine can be used to quantitatively assess the binding affinity of a single-stranded DNA to the protein system of interest via fluorescence spectroscopy, among other applications. We believe that this fluorescence binding assay is especially useful as its potentiality allows high-throughput screening of DNA–protein interactions.
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spelling pubmed-63848562019-02-23 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics Ahmed, Ismail A. Acharyya, Arusha Eng, Christina M. Rodgers, Jeffrey M. DeGrado, William F. Jo, Hyunil Gai, Feng Molecules Article Unnatural nucleosides possessing unique spectroscopic properties that mimic natural nucleobases in both size and chemical structure are ideally suited for spectroscopic measurements of DNA/RNA structure and dynamics in a site-specific manner. However, such unnatural nucleosides are scarce, which prompts us to explore the utility of a recently found unnatural nucleoside, 4-cyanoindole-2′-deoxyribonucleoside (4CNI-NS), as a site-specific spectroscopic probe of DNA. A recent study revealed that 4CNI-NS is a universal nucleobase that maintains the high fluorescence quantum yield of 4-cyanoindole and that among the four natural nucleobases, only guanine can significantly quench its fluorescence. Herein, we further show that the C≡N stretching frequency of 4CNI-NS is sensitive to the local environment, making it a useful site-specific infrared probe of oligonucleotides. In addition, we demonstrate that the fluorescence-quencher pair formed by 4CNI-NS and guanine can be used to quantitatively assess the binding affinity of a single-stranded DNA to the protein system of interest via fluorescence spectroscopy, among other applications. We believe that this fluorescence binding assay is especially useful as its potentiality allows high-throughput screening of DNA–protein interactions. MDPI 2019-02-08 /pmc/articles/PMC6384856/ /pubmed/30744004 http://dx.doi.org/10.3390/molecules24030602 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ahmed, Ismail A.
Acharyya, Arusha
Eng, Christina M.
Rodgers, Jeffrey M.
DeGrado, William F.
Jo, Hyunil
Gai, Feng
4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title_full 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title_fullStr 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title_full_unstemmed 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title_short 4-Cyanoindole-2′-deoxyribonucleoside as a Dual Fluorescence and Infrared Probe of DNA Structure and Dynamics
title_sort 4-cyanoindole-2′-deoxyribonucleoside as a dual fluorescence and infrared probe of dna structure and dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384856/
https://www.ncbi.nlm.nih.gov/pubmed/30744004
http://dx.doi.org/10.3390/molecules24030602
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