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Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment
Genomic DNA in eukaryotes is organized into chromatin through association with core histones to form nucleosomes, each distinguished by their DNA sequences and histone variants. Here, we used a single-chain antibody fragment (scFv) derived from the anti-nucleosome antibody mAb PL2-6 to stabilize hum...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534667/ https://www.ncbi.nlm.nih.gov/pubmed/31127102 http://dx.doi.org/10.1038/s41467-019-10247-4 |
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author | Zhou, Bing-Rui Yadav, K. N. Sathish Borgnia, Mario Hong, Jingjun Cao, Baohua Olins, Ada L. Olins, Donald E. Bai, Yawen Zhang, Ping |
author_facet | Zhou, Bing-Rui Yadav, K. N. Sathish Borgnia, Mario Hong, Jingjun Cao, Baohua Olins, Ada L. Olins, Donald E. Bai, Yawen Zhang, Ping |
author_sort | Zhou, Bing-Rui |
collection | PubMed |
description | Genomic DNA in eukaryotes is organized into chromatin through association with core histones to form nucleosomes, each distinguished by their DNA sequences and histone variants. Here, we used a single-chain antibody fragment (scFv) derived from the anti-nucleosome antibody mAb PL2-6 to stabilize human CENP-A nucleosome containing a native α-satellite DNA and solved its structure by the cryo-electron microscopy (cryo-EM) to 2.6 Å resolution. In comparison, the corresponding cryo-EM structure of the free CENP-A nucleosome could only reach 3.4 Å resolution. We find that scFv binds to a conserved acidic patch on the histone H2A-H2B dimer without perturbing the nucleosome structure. Our results provide an atomic resolution cryo-EM structure of a nucleosome and insight into the structure and function of the CENP-A nucleosome. The scFv approach is applicable to the structural determination of other native-like nucleosomes with distinct DNA sequences. |
format | Online Article Text |
id | pubmed-6534667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65346672019-05-28 Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment Zhou, Bing-Rui Yadav, K. N. Sathish Borgnia, Mario Hong, Jingjun Cao, Baohua Olins, Ada L. Olins, Donald E. Bai, Yawen Zhang, Ping Nat Commun Article Genomic DNA in eukaryotes is organized into chromatin through association with core histones to form nucleosomes, each distinguished by their DNA sequences and histone variants. Here, we used a single-chain antibody fragment (scFv) derived from the anti-nucleosome antibody mAb PL2-6 to stabilize human CENP-A nucleosome containing a native α-satellite DNA and solved its structure by the cryo-electron microscopy (cryo-EM) to 2.6 Å resolution. In comparison, the corresponding cryo-EM structure of the free CENP-A nucleosome could only reach 3.4 Å resolution. We find that scFv binds to a conserved acidic patch on the histone H2A-H2B dimer without perturbing the nucleosome structure. Our results provide an atomic resolution cryo-EM structure of a nucleosome and insight into the structure and function of the CENP-A nucleosome. The scFv approach is applicable to the structural determination of other native-like nucleosomes with distinct DNA sequences. Nature Publishing Group UK 2019-05-24 /pmc/articles/PMC6534667/ /pubmed/31127102 http://dx.doi.org/10.1038/s41467-019-10247-4 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2019 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhou, Bing-Rui Yadav, K. N. Sathish Borgnia, Mario Hong, Jingjun Cao, Baohua Olins, Ada L. Olins, Donald E. Bai, Yawen Zhang, Ping Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title | Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title_full | Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title_fullStr | Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title_full_unstemmed | Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title_short | Atomic resolution cryo-EM structure of a native-like CENP-A nucleosome aided by an antibody fragment |
title_sort | atomic resolution cryo-em structure of a native-like cenp-a nucleosome aided by an antibody fragment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534667/ https://www.ncbi.nlm.nih.gov/pubmed/31127102 http://dx.doi.org/10.1038/s41467-019-10247-4 |
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