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Photochemical modifications for DNA/RNA oligonucleotides

Light-triggered chemical reactions can provide excellent tools to investigate the fundamental mechanisms important in biology. Light is easily applicable and orthogonal to most cellular events, and its dose and locality can be controlled in tissues and cells. Light-induced conversion of photochemica...

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Detalles Bibliográficos
Autores principales: Tavakoli, Amirrasoul, Min, Jung-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982246/
https://www.ncbi.nlm.nih.gov/pubmed/35424630
http://dx.doi.org/10.1039/d1ra05951c
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author Tavakoli, Amirrasoul
Min, Jung-Hyun
author_facet Tavakoli, Amirrasoul
Min, Jung-Hyun
author_sort Tavakoli, Amirrasoul
collection PubMed
description Light-triggered chemical reactions can provide excellent tools to investigate the fundamental mechanisms important in biology. Light is easily applicable and orthogonal to most cellular events, and its dose and locality can be controlled in tissues and cells. Light-induced conversion of photochemical groups installed on small molecules, proteins, and oligonucleotides can alter their functional states and thus the ensuing biological events. Recently, photochemical control of DNA/RNA structure and function has garnered attention thanks to the rapidly expanding photochemistry used in diverse biological applications. Photoconvertible groups can be incorporated in the backbone, ribose, and nucleobase of an oligonucleotide to undergo various irreversible and reversible light-induced reactions such as cleavage, crosslinking, isomerization, and intramolecular cyclization reactions. In this review, we gather a list of photoconvertible groups used in oligonucleotides and summarize their reaction characteristics, impacts on DNA/RNA thermal stability and structure, as well as their biological applications.
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spelling pubmed-89822462022-04-13 Photochemical modifications for DNA/RNA oligonucleotides Tavakoli, Amirrasoul Min, Jung-Hyun RSC Adv Chemistry Light-triggered chemical reactions can provide excellent tools to investigate the fundamental mechanisms important in biology. Light is easily applicable and orthogonal to most cellular events, and its dose and locality can be controlled in tissues and cells. Light-induced conversion of photochemical groups installed on small molecules, proteins, and oligonucleotides can alter their functional states and thus the ensuing biological events. Recently, photochemical control of DNA/RNA structure and function has garnered attention thanks to the rapidly expanding photochemistry used in diverse biological applications. Photoconvertible groups can be incorporated in the backbone, ribose, and nucleobase of an oligonucleotide to undergo various irreversible and reversible light-induced reactions such as cleavage, crosslinking, isomerization, and intramolecular cyclization reactions. In this review, we gather a list of photoconvertible groups used in oligonucleotides and summarize their reaction characteristics, impacts on DNA/RNA thermal stability and structure, as well as their biological applications. The Royal Society of Chemistry 2022-02-24 /pmc/articles/PMC8982246/ /pubmed/35424630 http://dx.doi.org/10.1039/d1ra05951c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tavakoli, Amirrasoul
Min, Jung-Hyun
Photochemical modifications for DNA/RNA oligonucleotides
title Photochemical modifications for DNA/RNA oligonucleotides
title_full Photochemical modifications for DNA/RNA oligonucleotides
title_fullStr Photochemical modifications for DNA/RNA oligonucleotides
title_full_unstemmed Photochemical modifications for DNA/RNA oligonucleotides
title_short Photochemical modifications for DNA/RNA oligonucleotides
title_sort photochemical modifications for dna/rna oligonucleotides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982246/
https://www.ncbi.nlm.nih.gov/pubmed/35424630
http://dx.doi.org/10.1039/d1ra05951c
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