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Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array

M13 bacteriophage-based colorimetric sensors, especially multi-array sensors, have been successfully demonstrated to be a powerful platform for detecting extremely small amounts of target molecules. Colorimetric sensors can be fabricated easily using self-assembly of genetically engineered M13 bacte...

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Autores principales: Kim, Chuntae, Lee, Hansong, Devaraj, Vasanthan, Kim, Won-Geun, Lee, Yujin, Kim, Yeji, Jeong, Na-Na, Choi, Eun Jung, Baek, Sang Hong, Han, Dong-Wook, Sun, Hokeun, Oh, Jin-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023180/
https://www.ncbi.nlm.nih.gov/pubmed/31936438
http://dx.doi.org/10.3390/nano10010121
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author Kim, Chuntae
Lee, Hansong
Devaraj, Vasanthan
Kim, Won-Geun
Lee, Yujin
Kim, Yeji
Jeong, Na-Na
Choi, Eun Jung
Baek, Sang Hong
Han, Dong-Wook
Sun, Hokeun
Oh, Jin-Woo
author_facet Kim, Chuntae
Lee, Hansong
Devaraj, Vasanthan
Kim, Won-Geun
Lee, Yujin
Kim, Yeji
Jeong, Na-Na
Choi, Eun Jung
Baek, Sang Hong
Han, Dong-Wook
Sun, Hokeun
Oh, Jin-Woo
author_sort Kim, Chuntae
collection PubMed
description M13 bacteriophage-based colorimetric sensors, especially multi-array sensors, have been successfully demonstrated to be a powerful platform for detecting extremely small amounts of target molecules. Colorimetric sensors can be fabricated easily using self-assembly of genetically engineered M13 bacteriophage which incorporates peptide libraries on its surface. However, the ability to discriminate many types of target molecules is still required. In this work, we introduce a statistical method to efficiently analyze a huge amount of numerical results in order to classify various types of target molecules. To enhance the selectivity of M13 bacteriophage-based colorimetric sensors, a multi-array sensor system can be an appropriate platform. On this basis, a pattern-recognizing multi-array biosensor platform was fabricated by integrating three types of sensors in which genetically engineered M13 bacteriophages (wild-, RGD-, and EEEE-type) were utilized as a primary building block. This sensor system was used to analyze a pattern of color change caused by a reaction between the sensor array and external substances, followed by separating the specific target substances by means of hierarchical cluster analysis. The biosensor platform could detect drug contaminants such as hormone drugs (estrogen) and antibiotics. We expect that the proposed biosensor system could be used for the development of a first-analysis kit, which would be inexpensive and easy to supply and could be applied in monitoring the environment and health care.
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spelling pubmed-70231802020-03-12 Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array Kim, Chuntae Lee, Hansong Devaraj, Vasanthan Kim, Won-Geun Lee, Yujin Kim, Yeji Jeong, Na-Na Choi, Eun Jung Baek, Sang Hong Han, Dong-Wook Sun, Hokeun Oh, Jin-Woo Nanomaterials (Basel) Communication M13 bacteriophage-based colorimetric sensors, especially multi-array sensors, have been successfully demonstrated to be a powerful platform for detecting extremely small amounts of target molecules. Colorimetric sensors can be fabricated easily using self-assembly of genetically engineered M13 bacteriophage which incorporates peptide libraries on its surface. However, the ability to discriminate many types of target molecules is still required. In this work, we introduce a statistical method to efficiently analyze a huge amount of numerical results in order to classify various types of target molecules. To enhance the selectivity of M13 bacteriophage-based colorimetric sensors, a multi-array sensor system can be an appropriate platform. On this basis, a pattern-recognizing multi-array biosensor platform was fabricated by integrating three types of sensors in which genetically engineered M13 bacteriophages (wild-, RGD-, and EEEE-type) were utilized as a primary building block. This sensor system was used to analyze a pattern of color change caused by a reaction between the sensor array and external substances, followed by separating the specific target substances by means of hierarchical cluster analysis. The biosensor platform could detect drug contaminants such as hormone drugs (estrogen) and antibiotics. We expect that the proposed biosensor system could be used for the development of a first-analysis kit, which would be inexpensive and easy to supply and could be applied in monitoring the environment and health care. MDPI 2020-01-09 /pmc/articles/PMC7023180/ /pubmed/31936438 http://dx.doi.org/10.3390/nano10010121 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Kim, Chuntae
Lee, Hansong
Devaraj, Vasanthan
Kim, Won-Geun
Lee, Yujin
Kim, Yeji
Jeong, Na-Na
Choi, Eun Jung
Baek, Sang Hong
Han, Dong-Wook
Sun, Hokeun
Oh, Jin-Woo
Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title_full Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title_fullStr Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title_full_unstemmed Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title_short Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array
title_sort hierarchical cluster analysis of medical chemicals detected by a bacteriophage-based colorimetric sensor array
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023180/
https://www.ncbi.nlm.nih.gov/pubmed/31936438
http://dx.doi.org/10.3390/nano10010121
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