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Dimensional Reduction for Single-Molecule Imaging of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67
[Image: see text] Macromolecules organize themselves into discrete membrane-less compartments. Mounting evidence has suggested that nucleosomes as well as DNA itself can undergo clustering or condensation to regulate genomic activity. Current in vitro condensation studies provide insight into the ph...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009747/ https://www.ncbi.nlm.nih.gov/pubmed/36853329 http://dx.doi.org/10.1021/acs.jpcb.2c07011 |
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author | Benning, Nils A. Kæstel-Hansen, Jacob Rashid, Fahad Park, Sangwoo Merino Urteaga, Raquel Liao, Ting-Wei Hao, Jingzhou Berger, James M. Hatzakis, Nikos S. Ha, Taekjip |
author_facet | Benning, Nils A. Kæstel-Hansen, Jacob Rashid, Fahad Park, Sangwoo Merino Urteaga, Raquel Liao, Ting-Wei Hao, Jingzhou Berger, James M. Hatzakis, Nikos S. Ha, Taekjip |
author_sort | Benning, Nils A. |
collection | PubMed |
description | [Image: see text] Macromolecules organize themselves into discrete membrane-less compartments. Mounting evidence has suggested that nucleosomes as well as DNA itself can undergo clustering or condensation to regulate genomic activity. Current in vitro condensation studies provide insight into the physical properties of condensates, such as surface tension and diffusion. However, methods that provide the resolution needed for complex kinetic studies of multicomponent condensation are desired. Here, we use a supported lipid bilayer platform in tandem with total internal reflection microscopy to observe the two-dimensional movement of DNA and nucleosomes at the single-molecule resolution. This dimensional reduction from three-dimensional studies allows us to observe the initial condensation events and dissolution of these early condensates in the presence of physiological condensing agents. Using polyamines, we observed that the initial condensation happens on a time scale of minutes while dissolution occurs within seconds upon charge inversion. Polyamine valency, DNA length, and GC content affect the threshold polyamine concentration for condensation. Protein-based nucleosome condensing agents, HP1α and Ki-67, have much lower threshold concentrations for condensation than charge-based condensing agents, with Ki-67 being the most effective, requiring as low as 100 pM for nucleosome condensation. In addition, we did not observe condensate dissolution even at the highest concentrations of HP1α and Ki-67 tested. We also introduce a two-color imaging scheme where nucleosomes of high density labeled in one color are used to demarcate condensate boundaries and identical nucleosomes of another color at low density can be tracked relative to the boundaries after Ki-67-mediated condensation. Our platform should enable the ultimate resolution of single molecules in condensation dynamics studies of chromatin components under defined physicochemical conditions. |
format | Online Article Text |
id | pubmed-10009747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100097472023-03-14 Dimensional Reduction for Single-Molecule Imaging of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 Benning, Nils A. Kæstel-Hansen, Jacob Rashid, Fahad Park, Sangwoo Merino Urteaga, Raquel Liao, Ting-Wei Hao, Jingzhou Berger, James M. Hatzakis, Nikos S. Ha, Taekjip J Phys Chem B [Image: see text] Macromolecules organize themselves into discrete membrane-less compartments. Mounting evidence has suggested that nucleosomes as well as DNA itself can undergo clustering or condensation to regulate genomic activity. Current in vitro condensation studies provide insight into the physical properties of condensates, such as surface tension and diffusion. However, methods that provide the resolution needed for complex kinetic studies of multicomponent condensation are desired. Here, we use a supported lipid bilayer platform in tandem with total internal reflection microscopy to observe the two-dimensional movement of DNA and nucleosomes at the single-molecule resolution. This dimensional reduction from three-dimensional studies allows us to observe the initial condensation events and dissolution of these early condensates in the presence of physiological condensing agents. Using polyamines, we observed that the initial condensation happens on a time scale of minutes while dissolution occurs within seconds upon charge inversion. Polyamine valency, DNA length, and GC content affect the threshold polyamine concentration for condensation. Protein-based nucleosome condensing agents, HP1α and Ki-67, have much lower threshold concentrations for condensation than charge-based condensing agents, with Ki-67 being the most effective, requiring as low as 100 pM for nucleosome condensation. In addition, we did not observe condensate dissolution even at the highest concentrations of HP1α and Ki-67 tested. We also introduce a two-color imaging scheme where nucleosomes of high density labeled in one color are used to demarcate condensate boundaries and identical nucleosomes of another color at low density can be tracked relative to the boundaries after Ki-67-mediated condensation. Our platform should enable the ultimate resolution of single molecules in condensation dynamics studies of chromatin components under defined physicochemical conditions. American Chemical Society 2023-02-28 /pmc/articles/PMC10009747/ /pubmed/36853329 http://dx.doi.org/10.1021/acs.jpcb.2c07011 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Benning, Nils A. Kæstel-Hansen, Jacob Rashid, Fahad Park, Sangwoo Merino Urteaga, Raquel Liao, Ting-Wei Hao, Jingzhou Berger, James M. Hatzakis, Nikos S. Ha, Taekjip Dimensional Reduction for Single-Molecule Imaging of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title | Dimensional Reduction
for Single-Molecule Imaging
of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title_full | Dimensional Reduction
for Single-Molecule Imaging
of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title_fullStr | Dimensional Reduction
for Single-Molecule Imaging
of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title_full_unstemmed | Dimensional Reduction
for Single-Molecule Imaging
of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title_short | Dimensional Reduction
for Single-Molecule Imaging
of DNA and Nucleosome Condensation by Polyamines, HP1α and Ki-67 |
title_sort | dimensional reduction
for single-molecule imaging
of dna and nucleosome condensation by polyamines, hp1α and ki-67 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009747/ https://www.ncbi.nlm.nih.gov/pubmed/36853329 http://dx.doi.org/10.1021/acs.jpcb.2c07011 |
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