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Fast DNA Extraction with Polyacrylamide Microspheres for Polymerase Chain Reaction Detection
[Image: see text] The fast and cost-effective DNA extraction is critical for all DNA-based detections. Here, we fabricated a new kind of polyacrylamide microsphere (PAMMP) in various sizes with two methods, spot polymerization (large size but low yield) and modified inverse microemulsion polymerizat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301550/ https://www.ncbi.nlm.nih.gov/pubmed/32566849 http://dx.doi.org/10.1021/acsomega.0c01181 |
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author | Wang, Jun Zhang, Shuyan Xu, Xinhui Xing, Yujun Li, Zongru Wang, Jinke |
author_facet | Wang, Jun Zhang, Shuyan Xu, Xinhui Xing, Yujun Li, Zongru Wang, Jinke |
author_sort | Wang, Jun |
collection | PubMed |
description | [Image: see text] The fast and cost-effective DNA extraction is critical for all DNA-based detections. Here, we fabricated a new kind of polyacrylamide microsphere (PAMMP) in various sizes with two methods, spot polymerization (large size but low yield) and modified inverse microemulsion polymerization (small size but high yield). The fabricated PAMMPs have strong autofluorescence (fPAMMPs), including both visible fluorescence (VF) and near-infrared fluorescence (NIRF), which can remain very stable in various stringent conditions including strong acid and alkali and high temperature. The fabricated fPAMMPs were also highly positively charged, which could be used to effectively capture various biomolecules such as IRDye 800-labeled streptavidin and DNA. We thus developed a new method for rapid extraction (3–5 min) of DNA from various samples including bacteria, mammalian cells, plant and animal solid tissues, and human blood plasma using fPAMMPs. Moreover, the DNA captured on fPAMMPs (fPAMMP@DNA) could be effectively detected by both normal and quantitative PCR amplifications. Finally, we showed that NaBH(4) treatment removed autofluorescence in fPAMMPs (PAMMPs), which could also be applied to DNA extraction and PCR detection. In conclusion, we here fabricated new kinds of fPAMMPs and PAMMPs, developed a new rapid DNA extraction method, and demonstrated their useful applications in PCR detection. |
format | Online Article Text |
id | pubmed-7301550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73015502020-06-19 Fast DNA Extraction with Polyacrylamide Microspheres for Polymerase Chain Reaction Detection Wang, Jun Zhang, Shuyan Xu, Xinhui Xing, Yujun Li, Zongru Wang, Jinke ACS Omega [Image: see text] The fast and cost-effective DNA extraction is critical for all DNA-based detections. Here, we fabricated a new kind of polyacrylamide microsphere (PAMMP) in various sizes with two methods, spot polymerization (large size but low yield) and modified inverse microemulsion polymerization (small size but high yield). The fabricated PAMMPs have strong autofluorescence (fPAMMPs), including both visible fluorescence (VF) and near-infrared fluorescence (NIRF), which can remain very stable in various stringent conditions including strong acid and alkali and high temperature. The fabricated fPAMMPs were also highly positively charged, which could be used to effectively capture various biomolecules such as IRDye 800-labeled streptavidin and DNA. We thus developed a new method for rapid extraction (3–5 min) of DNA from various samples including bacteria, mammalian cells, plant and animal solid tissues, and human blood plasma using fPAMMPs. Moreover, the DNA captured on fPAMMPs (fPAMMP@DNA) could be effectively detected by both normal and quantitative PCR amplifications. Finally, we showed that NaBH(4) treatment removed autofluorescence in fPAMMPs (PAMMPs), which could also be applied to DNA extraction and PCR detection. In conclusion, we here fabricated new kinds of fPAMMPs and PAMMPs, developed a new rapid DNA extraction method, and demonstrated their useful applications in PCR detection. American Chemical Society 2020-06-04 /pmc/articles/PMC7301550/ /pubmed/32566849 http://dx.doi.org/10.1021/acsomega.0c01181 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Jun Zhang, Shuyan Xu, Xinhui Xing, Yujun Li, Zongru Wang, Jinke Fast DNA Extraction with Polyacrylamide Microspheres for Polymerase Chain Reaction Detection |
title | Fast DNA Extraction with Polyacrylamide Microspheres
for Polymerase Chain Reaction Detection |
title_full | Fast DNA Extraction with Polyacrylamide Microspheres
for Polymerase Chain Reaction Detection |
title_fullStr | Fast DNA Extraction with Polyacrylamide Microspheres
for Polymerase Chain Reaction Detection |
title_full_unstemmed | Fast DNA Extraction with Polyacrylamide Microspheres
for Polymerase Chain Reaction Detection |
title_short | Fast DNA Extraction with Polyacrylamide Microspheres
for Polymerase Chain Reaction Detection |
title_sort | fast dna extraction with polyacrylamide microspheres
for polymerase chain reaction detection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301550/ https://www.ncbi.nlm.nih.gov/pubmed/32566849 http://dx.doi.org/10.1021/acsomega.0c01181 |
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