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Fast antibody fragment motion: flexible linkers act as entropic spring
A flexible linker region between three fragments allows antibodies to adjust their binding sites to an antigen or receptor. Using Neutron Spin Echo Spectroscopy we observed fragment motion on a timescale of 7 ns with motional amplitudes of about 1 nm relative to each other. The mechanistic complexit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810366/ https://www.ncbi.nlm.nih.gov/pubmed/27020739 http://dx.doi.org/10.1038/srep22148 |
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author | Stingaciu, Laura R. Ivanova, Oxana Ohl, Michael Biehl, Ralf Richter, Dieter |
author_facet | Stingaciu, Laura R. Ivanova, Oxana Ohl, Michael Biehl, Ralf Richter, Dieter |
author_sort | Stingaciu, Laura R. |
collection | PubMed |
description | A flexible linker region between three fragments allows antibodies to adjust their binding sites to an antigen or receptor. Using Neutron Spin Echo Spectroscopy we observed fragment motion on a timescale of 7 ns with motional amplitudes of about 1 nm relative to each other. The mechanistic complexity of the linker region can be described by a spring model with Brownian motion of the fragments in a harmonic potential. Displacements, timescale, friction and force constant of the underlying dynamics are accessed. The force constant exhibits a similar strength to an entropic spring, with friction of the fragment matching the unbound state. The observed fast motions are fluctuations in pre-existing equilibrium configurations. The Brownian motion of domains in a harmonic potential is the appropriate model to examine functional hinge motions dependent on the structural topology and highlights the role of internal forces and friction to function. |
format | Online Article Text |
id | pubmed-4810366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48103662016-04-04 Fast antibody fragment motion: flexible linkers act as entropic spring Stingaciu, Laura R. Ivanova, Oxana Ohl, Michael Biehl, Ralf Richter, Dieter Sci Rep Article A flexible linker region between three fragments allows antibodies to adjust their binding sites to an antigen or receptor. Using Neutron Spin Echo Spectroscopy we observed fragment motion on a timescale of 7 ns with motional amplitudes of about 1 nm relative to each other. The mechanistic complexity of the linker region can be described by a spring model with Brownian motion of the fragments in a harmonic potential. Displacements, timescale, friction and force constant of the underlying dynamics are accessed. The force constant exhibits a similar strength to an entropic spring, with friction of the fragment matching the unbound state. The observed fast motions are fluctuations in pre-existing equilibrium configurations. The Brownian motion of domains in a harmonic potential is the appropriate model to examine functional hinge motions dependent on the structural topology and highlights the role of internal forces and friction to function. Nature Publishing Group 2016-03-29 /pmc/articles/PMC4810366/ /pubmed/27020739 http://dx.doi.org/10.1038/srep22148 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Stingaciu, Laura R. Ivanova, Oxana Ohl, Michael Biehl, Ralf Richter, Dieter Fast antibody fragment motion: flexible linkers act as entropic spring |
title | Fast antibody fragment motion: flexible linkers act as entropic spring |
title_full | Fast antibody fragment motion: flexible linkers act as entropic spring |
title_fullStr | Fast antibody fragment motion: flexible linkers act as entropic spring |
title_full_unstemmed | Fast antibody fragment motion: flexible linkers act as entropic spring |
title_short | Fast antibody fragment motion: flexible linkers act as entropic spring |
title_sort | fast antibody fragment motion: flexible linkers act as entropic spring |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810366/ https://www.ncbi.nlm.nih.gov/pubmed/27020739 http://dx.doi.org/10.1038/srep22148 |
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