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An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics
Single-molecule FRET (smFRET) has become a versatile tool for probing the structure and functional dynamics of biomolecular systems, and is extensively used to address questions ranging from biomolecular folding to drug discovery. Confocal smFRET measurements are amongst the widely used smFRET assay...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579363/ https://www.ncbi.nlm.nih.gov/pubmed/37845199 http://dx.doi.org/10.1038/s41467-023-42232-3 |
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author | Hartmann, Andreas Sreenivasa, Koushik Schenkel, Mathias Chamachi, Neharika Schake, Philipp Krainer, Georg Schlierf, Michael |
author_facet | Hartmann, Andreas Sreenivasa, Koushik Schenkel, Mathias Chamachi, Neharika Schake, Philipp Krainer, Georg Schlierf, Michael |
author_sort | Hartmann, Andreas |
collection | PubMed |
description | Single-molecule FRET (smFRET) has become a versatile tool for probing the structure and functional dynamics of biomolecular systems, and is extensively used to address questions ranging from biomolecular folding to drug discovery. Confocal smFRET measurements are amongst the widely used smFRET assays and are typically performed in a single-well format. Thus, sampling of many experimental parameters is laborious and time consuming. To address this challenge, we extend here the capabilities of confocal smFRET beyond single-well measurements by integrating a multiwell plate functionality to allow for continuous and automated smFRET measurements. We demonstrate the broad applicability of the multiwell plate assay towards DNA hairpin dynamics, protein folding, competitive and cooperative protein–DNA interactions, and drug-discovery, revealing insights that would be very difficult to achieve with conventional single-well format measurements. For the adaptation into existing instrumentations, we provide a detailed guide and open-source acquisition and analysis software. |
format | Online Article Text |
id | pubmed-10579363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105793632023-10-18 An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics Hartmann, Andreas Sreenivasa, Koushik Schenkel, Mathias Chamachi, Neharika Schake, Philipp Krainer, Georg Schlierf, Michael Nat Commun Article Single-molecule FRET (smFRET) has become a versatile tool for probing the structure and functional dynamics of biomolecular systems, and is extensively used to address questions ranging from biomolecular folding to drug discovery. Confocal smFRET measurements are amongst the widely used smFRET assays and are typically performed in a single-well format. Thus, sampling of many experimental parameters is laborious and time consuming. To address this challenge, we extend here the capabilities of confocal smFRET beyond single-well measurements by integrating a multiwell plate functionality to allow for continuous and automated smFRET measurements. We demonstrate the broad applicability of the multiwell plate assay towards DNA hairpin dynamics, protein folding, competitive and cooperative protein–DNA interactions, and drug-discovery, revealing insights that would be very difficult to achieve with conventional single-well format measurements. For the adaptation into existing instrumentations, we provide a detailed guide and open-source acquisition and analysis software. Nature Publishing Group UK 2023-10-16 /pmc/articles/PMC10579363/ /pubmed/37845199 http://dx.doi.org/10.1038/s41467-023-42232-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hartmann, Andreas Sreenivasa, Koushik Schenkel, Mathias Chamachi, Neharika Schake, Philipp Krainer, Georg Schlierf, Michael An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title | An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title_full | An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title_fullStr | An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title_full_unstemmed | An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title_short | An automated single-molecule FRET platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
title_sort | automated single-molecule fret platform for high-content, multiwell plate screening of biomolecular conformations and dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579363/ https://www.ncbi.nlm.nih.gov/pubmed/37845199 http://dx.doi.org/10.1038/s41467-023-42232-3 |
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