Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay

Mycoplasma pneumoniae is a highly infectious bacterium and the major cause of pneumonia especially in school-going children. Mycoplasma pneumoniae affects the respiratory tract, and 25% of patients experience health-related problems. It is important to have a suitable method to detect M. pneumoniae,...

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Main Authors: Qin, Dapeng, Gong, Qiuping, Li, Xin, Gao, Yanping, Gopinath, Subash C. B., Chen, Yeng, Yang, Zehua
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Published: Wiley 2023
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Online Access:http://eprints.um.edu.my/39509/
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Institution: Universiti Malaya
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spelling my.um.eprints.395092024-10-30T08:26:29Z http://eprints.um.edu.my/39509/ Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay Qin, Dapeng Gong, Qiuping Li, Xin Gao, Yanping Gopinath, Subash C. B. Chen, Yeng Yang, Zehua R Medicine RK Dentistry Oral surgery Mycoplasma pneumoniae is a highly infectious bacterium and the major cause of pneumonia especially in school-going children. Mycoplasma pneumoniae affects the respiratory tract, and 25% of patients experience health-related problems. It is important to have a suitable method to detect M. pneumoniae, and gold nanoparticle (GNP)-based colorimetric biosensing was used in this study to identify the specific target DNA for M. pneumoniae. The color of GNPs changes due to negatively charged GNPs in the presence of positively charged monovalent (Na+) ions from NaCl. This condition is reversed in the presence of a single-stranded oligonucleotide, as it attracts GNPs but not in the presence of double-stranded DNA. Single standard capture DNA was mixed with optimal target DNA that cannot be adsorbed by GNPs; under this condition, GNPs are not stabilized and aggregate at high ionic strength (from 100 mM). Without capture DNA, the GNPs that were stabilized by capture DNA (from 1 mu M) became more stable under high ionic conditions and retaining their red color. The GNPs turned blue in the presence of target DNA at concentrations of 1 pM, and the GNPs retained a red color when there was no target in the solution. This method is useful for the simple, easy, and accurate identification of M. pneumoniae target DNA at higher discrimination and without involving sophisticated equipment, and this method provides a diagnostic for M. pneumoniae. Wiley 2023-04 Article PeerReviewed Qin, Dapeng and Gong, Qiuping and Li, Xin and Gao, Yanping and Gopinath, Subash C. B. and Chen, Yeng and Yang, Zehua (2023) Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay. Biotechnology and Applied Biochemistry, 70 (2). pp. 553-559. ISSN 0885-4513, DOI https://doi.org/10.1002/bab.2377 <https://doi.org/10.1002/bab.2377>. 10.1002/bab.2377
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
RK Dentistry
Oral surgery
spellingShingle R Medicine
RK Dentistry
Oral surgery
Qin, Dapeng
Gong, Qiuping
Li, Xin
Gao, Yanping
Gopinath, Subash C. B.
Chen, Yeng
Yang, Zehua
Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
description Mycoplasma pneumoniae is a highly infectious bacterium and the major cause of pneumonia especially in school-going children. Mycoplasma pneumoniae affects the respiratory tract, and 25% of patients experience health-related problems. It is important to have a suitable method to detect M. pneumoniae, and gold nanoparticle (GNP)-based colorimetric biosensing was used in this study to identify the specific target DNA for M. pneumoniae. The color of GNPs changes due to negatively charged GNPs in the presence of positively charged monovalent (Na+) ions from NaCl. This condition is reversed in the presence of a single-stranded oligonucleotide, as it attracts GNPs but not in the presence of double-stranded DNA. Single standard capture DNA was mixed with optimal target DNA that cannot be adsorbed by GNPs; under this condition, GNPs are not stabilized and aggregate at high ionic strength (from 100 mM). Without capture DNA, the GNPs that were stabilized by capture DNA (from 1 mu M) became more stable under high ionic conditions and retaining their red color. The GNPs turned blue in the presence of target DNA at concentrations of 1 pM, and the GNPs retained a red color when there was no target in the solution. This method is useful for the simple, easy, and accurate identification of M. pneumoniae target DNA at higher discrimination and without involving sophisticated equipment, and this method provides a diagnostic for M. pneumoniae.
format Article
author Qin, Dapeng
Gong, Qiuping
Li, Xin
Gao, Yanping
Gopinath, Subash C. B.
Chen, Yeng
Yang, Zehua
author_facet Qin, Dapeng
Gong, Qiuping
Li, Xin
Gao, Yanping
Gopinath, Subash C. B.
Chen, Yeng
Yang, Zehua
author_sort Qin, Dapeng
title Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
title_short Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
title_full Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
title_fullStr Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
title_full_unstemmed Identification of Mycoplasma pneumoniae by DNA-modified gold nanomaterials in a colorimetric assay
title_sort identification of mycoplasma pneumoniae by dna-modified gold nanomaterials in a colorimetric assay
publisher Wiley
publishDate 2023
url http://eprints.um.edu.my/39509/
_version_ 1814933229042401280