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PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies
Chromatin immunoprecipitation (ChIP) is the most widely used approach for identification of genome-associated proteins and their modifications. We have previously introduced a microplate-based ChIP platform, Matrix ChIP, where the entire ChIP procedure is done on the same plate without sample transf...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614803/ https://www.ncbi.nlm.nih.gov/pubmed/30927002 http://dx.doi.org/10.1093/nar/gkz222 |
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author | Bomsztyk, Karol Mar, Daniel Wang, Yuliang Denisenko, Oleg Ware, Carol Frazar, Christian D Blattler, Adam Maxwell, Adam D MacConaghy, Brian E Matula, Thomas J |
author_facet | Bomsztyk, Karol Mar, Daniel Wang, Yuliang Denisenko, Oleg Ware, Carol Frazar, Christian D Blattler, Adam Maxwell, Adam D MacConaghy, Brian E Matula, Thomas J |
author_sort | Bomsztyk, Karol |
collection | PubMed |
description | Chromatin immunoprecipitation (ChIP) is the most widely used approach for identification of genome-associated proteins and their modifications. We have previously introduced a microplate-based ChIP platform, Matrix ChIP, where the entire ChIP procedure is done on the same plate without sample transfers. Compared to conventional ChIP protocols, the Matrix ChIP assay is faster and has increased throughput. However, even with microplate ChIP assays, sample preparation and chromatin fragmentation (which is required to map genomic locations) remains a major bottleneck. We have developed a novel technology (termed ‘PIXUL’) utilizing an array of ultrasound transducers for simultaneous shearing of samples in standard 96-well microplates. We integrated PIXUL with Matrix ChIP (‘PIXUL-ChIP’), that allows for fast, reproducible, low-cost and high-throughput sample preparation and ChIP analysis of 96 samples (cell culture or tissues) in one day. Further, we demonstrated that chromatin prepared using PIXUL can be used in an existing ChIP-seq workflow. Thus, the high-throughput capacity of PIXUL-ChIP provides the means to carry out ChIP-qPCR or ChIP-seq experiments involving dozens of samples. Given the complexity of epigenetic processes, the use of PIXUL-ChIP will advance our understanding of these processes in health and disease, as well as facilitate screening of epigenetic drugs. |
format | Online Article Text |
id | pubmed-6614803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66148032019-07-12 PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies Bomsztyk, Karol Mar, Daniel Wang, Yuliang Denisenko, Oleg Ware, Carol Frazar, Christian D Blattler, Adam Maxwell, Adam D MacConaghy, Brian E Matula, Thomas J Nucleic Acids Res Methods Online Chromatin immunoprecipitation (ChIP) is the most widely used approach for identification of genome-associated proteins and their modifications. We have previously introduced a microplate-based ChIP platform, Matrix ChIP, where the entire ChIP procedure is done on the same plate without sample transfers. Compared to conventional ChIP protocols, the Matrix ChIP assay is faster and has increased throughput. However, even with microplate ChIP assays, sample preparation and chromatin fragmentation (which is required to map genomic locations) remains a major bottleneck. We have developed a novel technology (termed ‘PIXUL’) utilizing an array of ultrasound transducers for simultaneous shearing of samples in standard 96-well microplates. We integrated PIXUL with Matrix ChIP (‘PIXUL-ChIP’), that allows for fast, reproducible, low-cost and high-throughput sample preparation and ChIP analysis of 96 samples (cell culture or tissues) in one day. Further, we demonstrated that chromatin prepared using PIXUL can be used in an existing ChIP-seq workflow. Thus, the high-throughput capacity of PIXUL-ChIP provides the means to carry out ChIP-qPCR or ChIP-seq experiments involving dozens of samples. Given the complexity of epigenetic processes, the use of PIXUL-ChIP will advance our understanding of these processes in health and disease, as well as facilitate screening of epigenetic drugs. Oxford University Press 2019-07-09 2019-03-30 /pmc/articles/PMC6614803/ /pubmed/30927002 http://dx.doi.org/10.1093/nar/gkz222 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Bomsztyk, Karol Mar, Daniel Wang, Yuliang Denisenko, Oleg Ware, Carol Frazar, Christian D Blattler, Adam Maxwell, Adam D MacConaghy, Brian E Matula, Thomas J PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title | PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title_full | PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title_fullStr | PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title_full_unstemmed | PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title_short | PIXUL-ChIP: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
title_sort | pixul-chip: integrated high-throughput sample preparation and analytical platform for epigenetic studies |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614803/ https://www.ncbi.nlm.nih.gov/pubmed/30927002 http://dx.doi.org/10.1093/nar/gkz222 |
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