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A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs
The chemically-synthesized siRNA duplex has become a powerful and widely used tool for RNAi loss-of-function studies, but suffers from a high off-target effect problem. Recently, endoribonulease-prepared siRNA (esiRNA) has been shown to be an attractive alternative due to its lower off-target effect...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384639/ https://www.ncbi.nlm.nih.gov/pubmed/22761791 http://dx.doi.org/10.1371/journal.pone.0039419 |
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author | Wang, Zhao Huang, Huang Zhang, Hanshuo Sun, Changhong Hao, Yang Yang, Junyu Fan, Yu Xi, Jianzhong Jeff |
author_facet | Wang, Zhao Huang, Huang Zhang, Hanshuo Sun, Changhong Hao, Yang Yang, Junyu Fan, Yu Xi, Jianzhong Jeff |
author_sort | Wang, Zhao |
collection | PubMed |
description | The chemically-synthesized siRNA duplex has become a powerful and widely used tool for RNAi loss-of-function studies, but suffers from a high off-target effect problem. Recently, endoribonulease-prepared siRNA (esiRNA) has been shown to be an attractive alternative due to its lower off-target effect and cost effectiveness. However, the current manufacturing method for esiRNA is complicated, mainly in regards to purification and normalization on a large-scale level. In this study, we present a magnetic bead-integrated chip that can immobilize amplification or transcription products on beads and accomplish transcription, digestion, normalization and purification in a robust and convenient manner. This chip is equipped to manufacture ready-to-use esiRNAs on a large-scale level. Silencing specificity and efficiency of these esiRNAs were validated at the transcriptional, translational and functional levels. Manufacture of several normalized esiRNAs in a single well, including those silencing PARP1 and BRCA1, was successfully achieved, and the esiRNAs were subsequently utilized to effectively investigate their synergistic effect on cell viability. A small esiRNA library targeting 68 tyrosine kinase genes was constructed for a loss-of-function study, and four genes were identified in regulating the migration capability of Hela cells. We believe that this approach provides a more robust and cost-effective choice for manufacturing esiRNAs than current approaches, and therefore these heterogeneous RNA strands may have utility in most intensive and extensive applications. |
format | Online Article Text |
id | pubmed-3384639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33846392012-07-03 A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs Wang, Zhao Huang, Huang Zhang, Hanshuo Sun, Changhong Hao, Yang Yang, Junyu Fan, Yu Xi, Jianzhong Jeff PLoS One Research Article The chemically-synthesized siRNA duplex has become a powerful and widely used tool for RNAi loss-of-function studies, but suffers from a high off-target effect problem. Recently, endoribonulease-prepared siRNA (esiRNA) has been shown to be an attractive alternative due to its lower off-target effect and cost effectiveness. However, the current manufacturing method for esiRNA is complicated, mainly in regards to purification and normalization on a large-scale level. In this study, we present a magnetic bead-integrated chip that can immobilize amplification or transcription products on beads and accomplish transcription, digestion, normalization and purification in a robust and convenient manner. This chip is equipped to manufacture ready-to-use esiRNAs on a large-scale level. Silencing specificity and efficiency of these esiRNAs were validated at the transcriptional, translational and functional levels. Manufacture of several normalized esiRNAs in a single well, including those silencing PARP1 and BRCA1, was successfully achieved, and the esiRNAs were subsequently utilized to effectively investigate their synergistic effect on cell viability. A small esiRNA library targeting 68 tyrosine kinase genes was constructed for a loss-of-function study, and four genes were identified in regulating the migration capability of Hela cells. We believe that this approach provides a more robust and cost-effective choice for manufacturing esiRNAs than current approaches, and therefore these heterogeneous RNA strands may have utility in most intensive and extensive applications. Public Library of Science 2012-06-27 /pmc/articles/PMC3384639/ /pubmed/22761791 http://dx.doi.org/10.1371/journal.pone.0039419 Text en Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Zhao Huang, Huang Zhang, Hanshuo Sun, Changhong Hao, Yang Yang, Junyu Fan, Yu Xi, Jianzhong Jeff A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title | A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title_full | A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title_fullStr | A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title_full_unstemmed | A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title_short | A Magnetic Bead-Integrated Chip for the Large Scale Manufacture of Normalized esiRNAs |
title_sort | magnetic bead-integrated chip for the large scale manufacture of normalized esirnas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384639/ https://www.ncbi.nlm.nih.gov/pubmed/22761791 http://dx.doi.org/10.1371/journal.pone.0039419 |
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