A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle

Changhyun Roh1, Ho-Young Lee2, Sang-Eun Kim2, Sung-Kee Jo11Radiation Research Division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Sinjeong-dong, Jeongeup, Jeonbuk, South Korea; 2Department of Nuclear Medicine, College of Medicin...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Changhyun Roh, Ho-Young Lee, Sang-Eun Kim, et al
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://doaj.org/article/73969957c4314c88b3260048601608c3
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:73969957c4314c88b3260048601608c3
record_format dspace
spelling oai:doaj.org-article:73969957c4314c88b3260048601608c32021-12-02T01:33:11ZA highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle1176-91141178-2013https://doaj.org/article/73969957c4314c88b3260048601608c32010-04-01T00:00:00Zhttp://www.dovepress.com/a-highly-sensitive-and-selective-viral-protein-detection-method-based--a4310https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Changhyun Roh1, Ho-Young Lee2, Sang-Eun Kim2, Sung-Kee Jo11Radiation Research Division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Sinjeong-dong, Jeongeup, Jeonbuk, South Korea; 2Department of Nuclear Medicine, College of Medicine, Seoul National University, South KoreaAbstract: Globally, approximately 170 million people (representing approximately 3% of the population worldwide), are infected with hepatitis C virus (HCV) and at risk of serious liver disease, including chronic hepatitis. We propose a new quantum dots (QDs)-supported RNA oligonucleotide approach for the specific and sensitive detection of viral protein using a biochip. This method was developed by immobilizing a HCV nonstructural protein 5B (NS5B) on the surface of a glass chip via the formation of a covalent bond between an amine protein group and a ProLinkerTM glass chip. The QDs-supported RNA oligonucleotide was conjugated via an amide formation reaction from coupling of a 5′-end-amine-modified RNA oligonucleotide on the surface of QDs displaying carboxyl groups via standard EDC coupling. The QDs-conjugated RNA oligonucleotide was interacted to immobilized viral protein NS5B on the biochip. The detection is based on the variation of signal of QDs-supported RNA oligonucleotide bound on an immobilized biochip. It was demonstrated that the value of the signal has a linear relationship with concentrations of the HCV NS5B viral protein in the 1 μg mL-1 to 1 ng mL-1 range with a detection limit of 1 ng mL-1. The major advantages of this RNA-oligonucleotide nanoparticle assay are its good specificity, ease of performance, and ability to perform one-spot monitoring. The proposed method could be used as a general method of HCV detection and is expected to be applicable to other types of diseases as well.Keywords: hepatitis C virus, viral protein, RNA oligonucleotide, quantum dots, biochip Changhyun RohHo-Young LeeSang-Eun Kimet alDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2010, Iss default, Pp 323-329 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Changhyun Roh
Ho-Young Lee
Sang-Eun Kim
et al
A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
description Changhyun Roh1, Ho-Young Lee2, Sang-Eun Kim2, Sung-Kee Jo11Radiation Research Division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Sinjeong-dong, Jeongeup, Jeonbuk, South Korea; 2Department of Nuclear Medicine, College of Medicine, Seoul National University, South KoreaAbstract: Globally, approximately 170 million people (representing approximately 3% of the population worldwide), are infected with hepatitis C virus (HCV) and at risk of serious liver disease, including chronic hepatitis. We propose a new quantum dots (QDs)-supported RNA oligonucleotide approach for the specific and sensitive detection of viral protein using a biochip. This method was developed by immobilizing a HCV nonstructural protein 5B (NS5B) on the surface of a glass chip via the formation of a covalent bond between an amine protein group and a ProLinkerTM glass chip. The QDs-supported RNA oligonucleotide was conjugated via an amide formation reaction from coupling of a 5′-end-amine-modified RNA oligonucleotide on the surface of QDs displaying carboxyl groups via standard EDC coupling. The QDs-conjugated RNA oligonucleotide was interacted to immobilized viral protein NS5B on the biochip. The detection is based on the variation of signal of QDs-supported RNA oligonucleotide bound on an immobilized biochip. It was demonstrated that the value of the signal has a linear relationship with concentrations of the HCV NS5B viral protein in the 1 μg mL-1 to 1 ng mL-1 range with a detection limit of 1 ng mL-1. The major advantages of this RNA-oligonucleotide nanoparticle assay are its good specificity, ease of performance, and ability to perform one-spot monitoring. The proposed method could be used as a general method of HCV detection and is expected to be applicable to other types of diseases as well.Keywords: hepatitis C virus, viral protein, RNA oligonucleotide, quantum dots, biochip
format article
author Changhyun Roh
Ho-Young Lee
Sang-Eun Kim
et al
author_facet Changhyun Roh
Ho-Young Lee
Sang-Eun Kim
et al
author_sort Changhyun Roh
title A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
title_short A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
title_full A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
title_fullStr A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
title_full_unstemmed A highly sensitive and selective viral protein detection method based on RNA oligonucleotide nanoparticle
title_sort highly sensitive and selective viral protein detection method based on rna oligonucleotide nanoparticle
publisher Dove Medical Press
publishDate 2010
url https://doaj.org/article/73969957c4314c88b3260048601608c3
work_keys_str_mv AT changhyunroh ahighlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT hoyounglee ahighlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT sangeunkim ahighlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT etal ahighlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT changhyunroh highlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT hoyounglee highlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT sangeunkim highlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
AT etal highlysensitiveandselectiveviralproteindetectionmethodbasedonrnaoligonucleotidenanoparticle
_version_ 1718403022898331648