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Application of Optical Protein-chip in Detecting Phage M13KO7
Avidin layer was bound on the substrate surface of Silicon wafer modified with aldehyde. The interaction between avidin and biotin was adopted for the immobilization of mouse monoclonal biotin-anti-M13 (antibody GP3)-labeled biotin. The surface was incubated in a solution containing phage M13KO7, wh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Institute of Microbiology, Chinese Academy of Sciences and Chinese Society for Microbiology. Published by Elsevier B.V.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148961/ https://www.ncbi.nlm.nih.gov/pubmed/17037215 http://dx.doi.org/10.1016/S1872-2075(06)60060-5 |
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author | QI, Cai FENG, Jing WANG, Zhan-Hui MENG, Yong-Hong YAN, Xi-Yun JIN, Gang |
author_facet | QI, Cai FENG, Jing WANG, Zhan-Hui MENG, Yong-Hong YAN, Xi-Yun JIN, Gang |
author_sort | QI, Cai |
collection | PubMed |
description | Avidin layer was bound on the substrate surface of Silicon wafer modified with aldehyde. The interaction between avidin and biotin was adopted for the immobilization of mouse monoclonal biotin-anti-M13 (antibody GP3)-labeled biotin. The surface was incubated in a solution containing phage M13KO7, which was trapped by the antibody GP3 with the interaction between phage M13KO7 and antibody GP3, resulting in a variation of layer thickness that was detected by imaging ellipsometry. The results showed a saturated layer of antibody GP3 with a thickness about 6.9 nm on the surface of the silicon wafer. The specific interaction between phage M13KO7 and antibody GP3 resulted in a variation of layer thickness. The layer of phage M13KO7 bound with antibody GP3 was 17.5 nm in the concentration of 1.1×10(10) pfu/mL. Each variation of the layer thickness corresponded to a concentration of phage M13KO7 in the range of 0.1×10(10)–2.5×10(10) pfu/mL, with the sensitivity of 10(9) pfu/mL. Compared with other methods, the optical protein-chip, requiring only short measurement time, label free, is a quantitative test, and can be visualized. This study could be significant on the interactions between the antibody and the virus, showing potential in the early diagnosis of virosis. |
format | Online Article Text |
id | pubmed-7148961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Institute of Microbiology, Chinese Academy of Sciences and Chinese Society for Microbiology. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71489612020-04-13 Application of Optical Protein-chip in Detecting Phage M13KO7 QI, Cai FENG, Jing WANG, Zhan-Hui MENG, Yong-Hong YAN, Xi-Yun JIN, Gang Sheng Wu Gong Cheng Xue Bao Research Paper Avidin layer was bound on the substrate surface of Silicon wafer modified with aldehyde. The interaction between avidin and biotin was adopted for the immobilization of mouse monoclonal biotin-anti-M13 (antibody GP3)-labeled biotin. The surface was incubated in a solution containing phage M13KO7, which was trapped by the antibody GP3 with the interaction between phage M13KO7 and antibody GP3, resulting in a variation of layer thickness that was detected by imaging ellipsometry. The results showed a saturated layer of antibody GP3 with a thickness about 6.9 nm on the surface of the silicon wafer. The specific interaction between phage M13KO7 and antibody GP3 resulted in a variation of layer thickness. The layer of phage M13KO7 bound with antibody GP3 was 17.5 nm in the concentration of 1.1×10(10) pfu/mL. Each variation of the layer thickness corresponded to a concentration of phage M13KO7 in the range of 0.1×10(10)–2.5×10(10) pfu/mL, with the sensitivity of 10(9) pfu/mL. Compared with other methods, the optical protein-chip, requiring only short measurement time, label free, is a quantitative test, and can be visualized. This study could be significant on the interactions between the antibody and the virus, showing potential in the early diagnosis of virosis. Institute of Microbiology, Chinese Academy of Sciences and Chinese Society for Microbiology. Published by Elsevier B.V. 2006-09 2006-10-10 /pmc/articles/PMC7148961/ /pubmed/17037215 http://dx.doi.org/10.1016/S1872-2075(06)60060-5 Text en Copyright © 2006 Institute of Microbiology, Chinese Academy of Sciences and Chinese Society for Microbiology. Published by 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 | Research Paper QI, Cai FENG, Jing WANG, Zhan-Hui MENG, Yong-Hong YAN, Xi-Yun JIN, Gang Application of Optical Protein-chip in Detecting Phage M13KO7 |
title | Application of Optical Protein-chip in Detecting Phage M13KO7 |
title_full | Application of Optical Protein-chip in Detecting Phage M13KO7 |
title_fullStr | Application of Optical Protein-chip in Detecting Phage M13KO7 |
title_full_unstemmed | Application of Optical Protein-chip in Detecting Phage M13KO7 |
title_short | Application of Optical Protein-chip in Detecting Phage M13KO7 |
title_sort | application of optical protein-chip in detecting phage m13ko7 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148961/ https://www.ncbi.nlm.nih.gov/pubmed/17037215 http://dx.doi.org/10.1016/S1872-2075(06)60060-5 |
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