Fluid flow in the sarcomere

A highly organized and densely packed lattice of molecular machinery within the sarcomeres of muscle cells powers contraction. Although many of the proteins that drive contraction have been studied extensively, the mechanical impact of fluid shearing within the lattice of molecular machinery has rec...

Full description

Bibliographic Details
Main Authors: Malingen, Sage A (Author), Hood, Kaitlyn Tuley (Author), Lauga, Eric (Author), Hosoi, Anette E. (Author), Daniel, Thomas L (Author)
Other Authors: Massachusetts Institute of Technology. Department of Mechanical Engineering (Contributor)
Format: Article
Language:English
Published: Elsevier BV, 2022-01-05T19:49:02Z.
Subjects:
Online Access:Get fulltext
LEADER 02056 am a22002413u 4500
001 138821.2
042 |a dc 
100 1 0 |a Malingen, Sage A  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Mechanical Engineering  |e contributor 
700 1 0 |a Hood, Kaitlyn Tuley  |e author 
700 1 0 |a Lauga, Eric  |e author 
700 1 0 |a Hosoi, Anette E.  |e author 
700 1 0 |a Daniel, Thomas L  |e author 
245 0 0 |a Fluid flow in the sarcomere 
260 |b Elsevier BV,   |c 2022-01-05T19:49:02Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/138821.2 
520 |a A highly organized and densely packed lattice of molecular machinery within the sarcomeres of muscle cells powers contraction. Although many of the proteins that drive contraction have been studied extensively, the mechanical impact of fluid shearing within the lattice of molecular machinery has received minimal attention. It was recently proposed that fluid flow augments substrate transport in the sarcomere, however, this analysis used analytical models of fluid flow in the molecular machinery that could not capture its full complexity. By building a finite element model of the sarcomere, we estimate the explicit flow field, and contrast it with analytical models. Our results demonstrate that viscous drag forces on sliding filaments are surprisingly small in contrast to the forces generated by single myosin molecular motors. This model also indicates that the energetic cost of fluid flow through viscous shearing with lattice proteins is likely minimal. The model also highlights a steep velocity gradient between sliding filaments and demonstrates that the maximal radial fluid velocity occurs near the tips of the filaments. To our knowledge, this is the first computational analysis of fluid flow within the highly structured sarcomere. 
520 |a Army Research Office (Contract W911NF-14-1-0396) 
520 |a NIH (Grant P30AR074990) 
546 |a en 
655 7 |a Article 
773 |t 10.1016/J.ABB.2021.108923 
773 |t Archives of Biochemistry and Biophysics