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G-quadruplex-based aptamers against protein targets in therapy and diagnostics()

Nucleic acid aptamers are single-stranded DNA or RNA molecules identified to recognize with high affinity specific targets including proteins, small molecules, ions, whole cells and even entire organisms, such as viruses or bacteria. They can be identified from combinatorial libraries of DNA or RNA...

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Autores principales: Platella, Chiara, Riccardi, Claudia, Montesarchio, Daniela, Roviello, Giovanni N., Musumeci, Domenica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117017/
https://www.ncbi.nlm.nih.gov/pubmed/27865995
http://dx.doi.org/10.1016/j.bbagen.2016.11.027
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author Platella, Chiara
Riccardi, Claudia
Montesarchio, Daniela
Roviello, Giovanni N.
Musumeci, Domenica
author_facet Platella, Chiara
Riccardi, Claudia
Montesarchio, Daniela
Roviello, Giovanni N.
Musumeci, Domenica
author_sort Platella, Chiara
collection PubMed
description Nucleic acid aptamers are single-stranded DNA or RNA molecules identified to recognize with high affinity specific targets including proteins, small molecules, ions, whole cells and even entire organisms, such as viruses or bacteria. They can be identified from combinatorial libraries of DNA or RNA oligonucleotides by SELEX technology, an in vitro iterative selection procedure consisting of binding (capture), partitioning and amplification steps. Remarkably, many of the aptamers selected against biologically relevant protein targets are G-rich sequences that can fold into stable G-quadruplex (G4) structures. Aiming at disseminating novel inspiring ideas within the scientific community in the field of G4-structures, the emphasis of this review is placed on: 1) recent advancements in SELEX technology for the efficient and rapid identification of new candidate aptamers (introduction of microfluidic systems and next generation sequencing); 2) recurrence of G4 structures in aptamers selected by SELEX against biologically relevant protein targets; 3) discovery of several G4-forming motifs in important regulatory regions of the human or viral genome bound by endogenous proteins, which per se can result into potential aptamers; 4) an updated overview of G4-based aptamers with therapeutic potential and 5) a discussion on the most attractive G4-based aptamers for diagnostic applications. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.
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spelling pubmed-71170172020-04-02 G-quadruplex-based aptamers against protein targets in therapy and diagnostics() Platella, Chiara Riccardi, Claudia Montesarchio, Daniela Roviello, Giovanni N. Musumeci, Domenica Biochim Biophys Acta Gen Subj Article Nucleic acid aptamers are single-stranded DNA or RNA molecules identified to recognize with high affinity specific targets including proteins, small molecules, ions, whole cells and even entire organisms, such as viruses or bacteria. They can be identified from combinatorial libraries of DNA or RNA oligonucleotides by SELEX technology, an in vitro iterative selection procedure consisting of binding (capture), partitioning and amplification steps. Remarkably, many of the aptamers selected against biologically relevant protein targets are G-rich sequences that can fold into stable G-quadruplex (G4) structures. Aiming at disseminating novel inspiring ideas within the scientific community in the field of G4-structures, the emphasis of this review is placed on: 1) recent advancements in SELEX technology for the efficient and rapid identification of new candidate aptamers (introduction of microfluidic systems and next generation sequencing); 2) recurrence of G4 structures in aptamers selected by SELEX against biologically relevant protein targets; 3) discovery of several G4-forming motifs in important regulatory regions of the human or viral genome bound by endogenous proteins, which per se can result into potential aptamers; 4) an updated overview of G4-based aptamers with therapeutic potential and 5) a discussion on the most attractive G4-based aptamers for diagnostic applications. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio. Elsevier B.V. 2017-05 2016-11-16 /pmc/articles/PMC7117017/ /pubmed/27865995 http://dx.doi.org/10.1016/j.bbagen.2016.11.027 Text en © 2016 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Platella, Chiara
Riccardi, Claudia
Montesarchio, Daniela
Roviello, Giovanni N.
Musumeci, Domenica
G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title_full G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title_fullStr G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title_full_unstemmed G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title_short G-quadruplex-based aptamers against protein targets in therapy and diagnostics()
title_sort g-quadruplex-based aptamers against protein targets in therapy and diagnostics()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117017/
https://www.ncbi.nlm.nih.gov/pubmed/27865995
http://dx.doi.org/10.1016/j.bbagen.2016.11.027
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