Nucleic acid binding and other biomedical properties of artificial oligolysines

Giovanni N Roviello,1 Caterina Vicidomini,1 Vincenzo Costanzo,1 Valentina Roviello2 1CNR Istituto di Biostrutture e Bioimmagini, Via Mezzocannone site and Headquarters, 2Centro Regionale di Competenza (CRdC) Tecnologie, Via Nuova Agnano, Napoli, Italy Abstract: In the present study, we report the in...

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Main Authors: Roviello GN, Vicidomini C, Costanzo V, Roviello V
Format: Article
Language:English
Published: Dove Medical Press 2016-11-01
Series:International Journal of Nanomedicine
Subjects:
Online Access:https://www.dovepress.com/nucleic-acid-binding-and-other-biomedical-properties-of-artificial-oli-peer-reviewed-article-IJN
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author Roviello GN
Vicidomini C
Costanzo V
Roviello V
author_facet Roviello GN
Vicidomini C
Costanzo V
Roviello V
author_sort Roviello GN
collection DOAJ
description Giovanni N Roviello,1 Caterina Vicidomini,1 Vincenzo Costanzo,1 Valentina Roviello2 1CNR Istituto di Biostrutture e Bioimmagini, Via Mezzocannone site and Headquarters, 2Centro Regionale di Competenza (CRdC) Tecnologie, Via Nuova Agnano, Napoli, Italy Abstract: In the present study, we report the interaction of an artificial oligolysine (referred to as AOL) realized in our laboratory with targets of biomedical importance. These included polyinosinic acid (poly rI) and its complex with polycytidylic acid (poly I:C), RNAs with well-known interferon-inducing ability, and double-stranded (ds) DNA. The ability of the peptide to bind both single-stranded poly rI and ds poly I:C RNAs emerged from our circular dichroism (CD) and ultraviolet (UV) studies. In addition, we found that AOL forms complexes with dsDNA, as shown by spectroscopic binding assays and UV thermal denaturation experiments. These findings are encouraging for the possible use of AOL in biomedicine for nucleic acid targeting and oligonucleotide condensation, with the latter being a key step preceding their clinical application. Moreover, we tested the ability of AOL to bind to proteins, using serum albumin as a model protein. We demonstrated the oligolysine–protein binding by CD experiments which suggested that AOL, positively charged under physiological conditions, binds to the protein regions rich in anionic residues. Finally, the morphology characterization of the solid oligolysine, performed by scanning electron microscopy, showed different crystal forms including cubic-shaped crystals confirming the high purity of AOL. Keywords: nucleic acid binding, polyinosinic acid, double-stranded nucleic acids, oligolysine, circular dichroism
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spelling doaj.art-052bdc7c2d7e426f8cd229891315c9bf2022-12-21T18:00:39ZengDove Medical PressInternational Journal of Nanomedicine1178-20132016-11-01Volume 115897590429967Nucleic acid binding and other biomedical properties of artificial oligolysinesRoviello GNVicidomini CCostanzo VRoviello VGiovanni N Roviello,1 Caterina Vicidomini,1 Vincenzo Costanzo,1 Valentina Roviello2 1CNR Istituto di Biostrutture e Bioimmagini, Via Mezzocannone site and Headquarters, 2Centro Regionale di Competenza (CRdC) Tecnologie, Via Nuova Agnano, Napoli, Italy Abstract: In the present study, we report the interaction of an artificial oligolysine (referred to as AOL) realized in our laboratory with targets of biomedical importance. These included polyinosinic acid (poly rI) and its complex with polycytidylic acid (poly I:C), RNAs with well-known interferon-inducing ability, and double-stranded (ds) DNA. The ability of the peptide to bind both single-stranded poly rI and ds poly I:C RNAs emerged from our circular dichroism (CD) and ultraviolet (UV) studies. In addition, we found that AOL forms complexes with dsDNA, as shown by spectroscopic binding assays and UV thermal denaturation experiments. These findings are encouraging for the possible use of AOL in biomedicine for nucleic acid targeting and oligonucleotide condensation, with the latter being a key step preceding their clinical application. Moreover, we tested the ability of AOL to bind to proteins, using serum albumin as a model protein. We demonstrated the oligolysine–protein binding by CD experiments which suggested that AOL, positively charged under physiological conditions, binds to the protein regions rich in anionic residues. Finally, the morphology characterization of the solid oligolysine, performed by scanning electron microscopy, showed different crystal forms including cubic-shaped crystals confirming the high purity of AOL. Keywords: nucleic acid binding, polyinosinic acid, double-stranded nucleic acids, oligolysine, circular dichroismhttps://www.dovepress.com/nucleic-acid-binding-and-other-biomedical-properties-of-artificial-oli-peer-reviewed-article-IJNnucleic acid bindingpolyinosinic aciddouble-stranded nucleic acidsoligolysinecircular dichroism
spellingShingle Roviello GN
Vicidomini C
Costanzo V
Roviello V
Nucleic acid binding and other biomedical properties of artificial oligolysines
International Journal of Nanomedicine
nucleic acid binding
polyinosinic acid
double-stranded nucleic acids
oligolysine
circular dichroism
title Nucleic acid binding and other biomedical properties of artificial oligolysines
title_full Nucleic acid binding and other biomedical properties of artificial oligolysines
title_fullStr Nucleic acid binding and other biomedical properties of artificial oligolysines
title_full_unstemmed Nucleic acid binding and other biomedical properties of artificial oligolysines
title_short Nucleic acid binding and other biomedical properties of artificial oligolysines
title_sort nucleic acid binding and other biomedical properties of artificial oligolysines
topic nucleic acid binding
polyinosinic acid
double-stranded nucleic acids
oligolysine
circular dichroism
url https://www.dovepress.com/nucleic-acid-binding-and-other-biomedical-properties-of-artificial-oli-peer-reviewed-article-IJN
work_keys_str_mv AT roviellogn nucleicacidbindingandotherbiomedicalpropertiesofartificialoligolysines
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AT costanzov nucleicacidbindingandotherbiomedicalpropertiesofartificialoligolysines
AT roviellov nucleicacidbindingandotherbiomedicalpropertiesofartificialoligolysines