Literature DB >> 31468044

Brownian dynamics assessment of enhanced diffusion exhibited by 'fluctuating-dumbbell enzymes'.

Svyatoslav Kondrat1, Mihail N Popescu2.   

Abstract

Recent experiments have reported that diffusion of enzymes can be enhanced in the presence of their substrates. Using a fluctuating dumbbell model of enzymes, it has been argued that such an enhancement can be rationalized by the reduction of the enzyme size and by the suppression of the hydrodynamically coupled conformational fluctuations, induced by binding a substrate or an inhibitor to the enzyme [Nano Lett. 2017, 17, 4415]. Herein, we critically examine these expectations via extensive Brownian dynamics simulations of a similar model. The numerical results show that neither of the two mechanisms can cause an enhancement comparable to that reported experimentally, unless very large, physically counter-intuitive, enzyme deformations are invoked.

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Year:  2019        PMID: 31468044     DOI: 10.1039/c9cp02842k

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  2 in total

1.  A thermodynamic perspective on enhanced enzyme diffusion.

Authors:  Steve Pressé
Journal:  Proc Natl Acad Sci U S A       Date:  2020-12-09       Impact factor: 12.779

Review 2.  Perspective: a stirring role for metabolism in cells.

Authors:  José Losa; Simeon Leupold; Diego Alonso-Martinez; Petteri Vainikka; Sebastian Thallmair; Katarzyna M Tych; Siewert J Marrink; Matthias Heinemann
Journal:  Mol Syst Biol       Date:  2022-04       Impact factor: 11.429

  2 in total

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