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....

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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