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Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules
Cooperativity, a universal property of biological macromolecules, is typically characterized by a Hill slope, which can provide fundamental information about binding sites and interactions. We demonstrate, via simulations and single molecule FRET experiments, that molecular heterogeneity lowers bulk...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3109240/ https://www.ncbi.nlm.nih.gov/pubmed/21572445 http://dx.doi.org/10.1038/nsmb.2052 |
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author | Solomatin, Sergey V. Greenfeld, Max Herschlag, Daniel |
author_facet | Solomatin, Sergey V. Greenfeld, Max Herschlag, Daniel |
author_sort | Solomatin, Sergey V. |
collection | PubMed |
description | Cooperativity, a universal property of biological macromolecules, is typically characterized by a Hill slope, which can provide fundamental information about binding sites and interactions. We demonstrate, via simulations and single molecule FRET experiments, that molecular heterogeneity lowers bulk cooperativity from the intrinsic value for the individual molecules. As heterogeneity is common in smFRET experiments, appreciation of its influence on fundamental measures of cooperativity is critical for deriving accurate molecular models. |
format | Online Article Text |
id | pubmed-3109240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-31092402011-12-01 Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules Solomatin, Sergey V. Greenfeld, Max Herschlag, Daniel Nat Struct Mol Biol Article Cooperativity, a universal property of biological macromolecules, is typically characterized by a Hill slope, which can provide fundamental information about binding sites and interactions. We demonstrate, via simulations and single molecule FRET experiments, that molecular heterogeneity lowers bulk cooperativity from the intrinsic value for the individual molecules. As heterogeneity is common in smFRET experiments, appreciation of its influence on fundamental measures of cooperativity is critical for deriving accurate molecular models. 2011-05-15 2011-06 /pmc/articles/PMC3109240/ /pubmed/21572445 http://dx.doi.org/10.1038/nsmb.2052 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Solomatin, Sergey V. Greenfeld, Max Herschlag, Daniel Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title | Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title_full | Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title_fullStr | Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title_full_unstemmed | Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title_short | Implications of Molecular Heterogeneity for the Cooperativity of Biological Macromolecules |
title_sort | implications of molecular heterogeneity for the cooperativity of biological macromolecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3109240/ https://www.ncbi.nlm.nih.gov/pubmed/21572445 http://dx.doi.org/10.1038/nsmb.2052 |
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