IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-48016-7.html
   My bibliography  Save this article

The role of memory-dependent friction and solvent viscosity in isomerization kinetics in viscogenic media

Author

Listed:
  • Benjamin A. Dalton

    (Fachbereich Physik)

  • Henrik Kiefer

    (Fachbereich Physik)

  • Roland R. Netz

    (Fachbereich Physik)

Abstract

Molecular isomerization kinetics in liquid solvent depends on a complex interplay between the solvent friction acting on the molecule, internal dissipation effects (also known as internal friction), the viscosity of the solvent, and the dihedral free energy profile. Due to the absence of accurate techniques to directly evaluate isomerization friction, it has not been possible to explore these relationships in full. By combining extensive molecular dynamics simulations with friction memory-kernel extraction techniques we consider a variety of small, isomerising molecules under a range of different viscogenic conditions and directly evaluate the viscosity dependence of the friction acting on a rotating dihedral. We reveal that the influence of different viscogenic media on isomerization kinetics can be dramatically different, even when measured at the same viscosity. This is due to the dynamic solute-solvent coupling, mediated by time-dependent friction memory kernels. We also show that deviations from the linear dependence of isomerization rates on solvent viscosity, which are often simply attributed to internal friction effects, are due to the simultaneous violation of two fundamental relationships: the Stokes-Einstein relation and the overdamped Kramers prediction for the barrier-crossing rate, both of which require explicit knowledge of friction.

Suggested Citation

  • Benjamin A. Dalton & Henrik Kiefer & Roland R. Netz, 2024. "The role of memory-dependent friction and solvent viscosity in isomerization kinetics in viscogenic media," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48016-7
    DOI: 10.1038/s41467-024-48016-7
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-48016-7
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-48016-7?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. David de Sancho & Anshul Sirur & Robert B. Best, 2014. "Molecular origins of internal friction effects on protein-folding rates," Nature Communications, Nature, vol. 5(1), pages 1-10, September.
    2. Alessandro Borgia & Beth G. Wensley & Andrea Soranno & Daniel Nettels & Madeleine B. Borgia & Armin Hoffmann & Shawn H. Pfeil & Everett A. Lipman & Jane Clarke & Benjamin Schuler, 2012. "Localizing internal friction along the reaction coordinate of protein folding by combining ensemble and single-molecule fluorescence spectroscopy," Nature Communications, Nature, vol. 3(1), pages 1-9, January.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Kirill Zinovjev & Paul Guénon & Carlos A. Ramos-Guzmán & J. Javier Ruiz-Pernía & Damien Laage & Iñaki Tuñón, 2024. "Activation and friction in enzymatic loop opening and closing dynamics," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48016-7. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.