Cargando…
Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules
Protein adsorption to solid carbohydrate interfaces is critical to many biological processes, particularly in biomass deconstruction. To engineer more-efficient enzymes for biomass deconstruction into sugars, it is necessary to characterize the complex protein–carbohydrate interfacial interactions....
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586272/ https://www.ncbi.nlm.nih.gov/pubmed/36215467 http://dx.doi.org/10.1073/pnas.2117467119 |
_version_ | 1784813654722478080 |
---|---|
author | Hackl, Markus Contrada, Edward V. Ash, Jonathan E. Kulkarni, Atharv Yoon, Jinho Cho, Hyeon-Yeol Lee, Ki-Bum Yarbrough, John M. López, Cesar A. Gnanakaran, Sandrasegaram Chundawat, Shishir P. S. |
author_facet | Hackl, Markus Contrada, Edward V. Ash, Jonathan E. Kulkarni, Atharv Yoon, Jinho Cho, Hyeon-Yeol Lee, Ki-Bum Yarbrough, John M. López, Cesar A. Gnanakaran, Sandrasegaram Chundawat, Shishir P. S. |
author_sort | Hackl, Markus |
collection | PubMed |
description | Protein adsorption to solid carbohydrate interfaces is critical to many biological processes, particularly in biomass deconstruction. To engineer more-efficient enzymes for biomass deconstruction into sugars, it is necessary to characterize the complex protein–carbohydrate interfacial interactions. A carbohydrate-binding module (CBM) is often associated with microbial surface-tethered cellulosomes or secreted cellulase enzymes to enhance substrate accessibility. However, it is not well known how CBMs recognize, bind, and dissociate from polysaccharides to facilitate efficient cellulolytic activity, due to the lack of mechanistic understanding and a suitable toolkit to study CBM–substrate interactions. Our work outlines a general approach to study the unbinding behavior of CBMs from polysaccharide surfaces using a highly multiplexed single-molecule force spectroscopy assay. Here, we apply acoustic force spectroscopy (AFS) to probe a Clostridium thermocellum cellulosomal scaffoldin protein (CBM3a) and measure its dissociation from nanocellulose surfaces at physiologically relevant, low force loading rates. An automated microfluidic setup and method for uniform deposition of insoluble polysaccharides on the AFS chip surfaces are demonstrated. The rupture forces of wild-type CBM3a, and its Y67A mutant, unbinding from nanocellulose surfaces suggests distinct multimodal CBM binding conformations, with structural mechanisms further explored using molecular dynamics simulations. Applying classical dynamic force spectroscopy theory, the single-molecule unbinding rate at zero force is extrapolated and found to agree with bulk equilibrium unbinding rates estimated independently using quartz crystal microbalance with dissipation monitoring. However, our results also highlight critical limitations of applying classical theory to explain the highly multivalent binding interactions for cellulose–CBM bond rupture forces exceeding 15 pN. |
format | Online Article Text |
id | pubmed-9586272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-95862722023-04-10 Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules Hackl, Markus Contrada, Edward V. Ash, Jonathan E. Kulkarni, Atharv Yoon, Jinho Cho, Hyeon-Yeol Lee, Ki-Bum Yarbrough, John M. López, Cesar A. Gnanakaran, Sandrasegaram Chundawat, Shishir P. S. Proc Natl Acad Sci U S A Biological Sciences Protein adsorption to solid carbohydrate interfaces is critical to many biological processes, particularly in biomass deconstruction. To engineer more-efficient enzymes for biomass deconstruction into sugars, it is necessary to characterize the complex protein–carbohydrate interfacial interactions. A carbohydrate-binding module (CBM) is often associated with microbial surface-tethered cellulosomes or secreted cellulase enzymes to enhance substrate accessibility. However, it is not well known how CBMs recognize, bind, and dissociate from polysaccharides to facilitate efficient cellulolytic activity, due to the lack of mechanistic understanding and a suitable toolkit to study CBM–substrate interactions. Our work outlines a general approach to study the unbinding behavior of CBMs from polysaccharide surfaces using a highly multiplexed single-molecule force spectroscopy assay. Here, we apply acoustic force spectroscopy (AFS) to probe a Clostridium thermocellum cellulosomal scaffoldin protein (CBM3a) and measure its dissociation from nanocellulose surfaces at physiologically relevant, low force loading rates. An automated microfluidic setup and method for uniform deposition of insoluble polysaccharides on the AFS chip surfaces are demonstrated. The rupture forces of wild-type CBM3a, and its Y67A mutant, unbinding from nanocellulose surfaces suggests distinct multimodal CBM binding conformations, with structural mechanisms further explored using molecular dynamics simulations. Applying classical dynamic force spectroscopy theory, the single-molecule unbinding rate at zero force is extrapolated and found to agree with bulk equilibrium unbinding rates estimated independently using quartz crystal microbalance with dissipation monitoring. However, our results also highlight critical limitations of applying classical theory to explain the highly multivalent binding interactions for cellulose–CBM bond rupture forces exceeding 15 pN. National Academy of Sciences 2022-10-10 2022-10-18 /pmc/articles/PMC9586272/ /pubmed/36215467 http://dx.doi.org/10.1073/pnas.2117467119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Hackl, Markus Contrada, Edward V. Ash, Jonathan E. Kulkarni, Atharv Yoon, Jinho Cho, Hyeon-Yeol Lee, Ki-Bum Yarbrough, John M. López, Cesar A. Gnanakaran, Sandrasegaram Chundawat, Shishir P. S. Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title | Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title_full | Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title_fullStr | Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title_full_unstemmed | Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title_short | Acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
title_sort | acoustic force spectroscopy reveals subtle differences in cellulose unbinding behavior of carbohydrate-binding modules |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586272/ https://www.ncbi.nlm.nih.gov/pubmed/36215467 http://dx.doi.org/10.1073/pnas.2117467119 |
work_keys_str_mv | AT hacklmarkus acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT contradaedwardv acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT ashjonathane acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT kulkarniatharv acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT yoonjinho acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT chohyeonyeol acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT leekibum acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT yarbroughjohnm acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT lopezcesara acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT gnanakaransandrasegaram acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules AT chundawatshishirps acousticforcespectroscopyrevealssubtledifferencesincelluloseunbindingbehaviorofcarbohydratebindingmodules |