Literature DB >> 32709625

In vivo X-ray diffraction and simultaneous EMG reveal the time course of myofilament lattice dilation and filament stretch.

Sage A Malingen1, Anthony M Asencio2, Julie A Cass3, Weikang Ma4, Thomas C Irving4, Thomas L Daniel1.   

Abstract

Muscle function within an organism depends on the feedback between molecular and meter-scale processes. Although the motions of muscle's contractile machinery are well described in isolated preparations, only a handful of experiments have documented the kinematics of the lattice occurring when multi-scale interactions are fully intact. We used time-resolved X-ray diffraction to record the kinematics of the myofilament lattice within a normal operating context: the tethered flight of Manduca sexta As the primary flight muscles of M . sexta are synchronous, we used these results to reveal the timing of in vivo cross-bridge recruitment, which occurred 24 ms (s.d. 26) following activation. In addition, the thick filaments stretched an average of 0.75% (s.d. 0.32) and thin filaments stretched 1.11% (s.d. 0.65). In contrast to other in vivo preparations, lattice spacing changed an average of 2.72% (s.d. 1.47). Lattice dilation of this magnitude significantly affects shortening velocity and force generation, and filament stretching tunes force generation. While the kinematics were consistent within individual trials, there was extensive variation between trials. Using a mechanism-free machine learning model we searched for patterns within and across trials. Although lattice kinematics were predictable within trials, the model could not create predictions across trials. This indicates that the variability we see across trials may be explained by latent variables occurring in this naturally functioning system. The diverse kinematic combinations we documented mirror muscle's adaptability and may facilitate its robust function in unpredictable conditions.
© 2020. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Myofilament lattice dynamics; Sarcomere; Structure–function

Mesh:

Year:  2020        PMID: 32709625      PMCID: PMC7490515          DOI: 10.1242/jeb.224188

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


  44 in total

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5.  A Spatially Explicit Model Shows How Titin Stiffness Modulates Muscle Mechanics and Energetics.

Authors:  Joseph D Powers; C David Williams; Michael Regnier; Thomas L Daniel
Journal:  Integr Comp Biol       Date:  2018-08-01       Impact factor: 3.326

6.  In vivo X-ray diffraction and simultaneous EMG reveal the time course of myofilament lattice dilation and filament stretch.

Authors:  Sage A Malingen; Anthony M Asencio; Julie A Cass; Weikang Ma; Thomas C Irving; Thomas L Daniel
Journal:  J Exp Biol       Date:  2020-09-03       Impact factor: 3.312

7.  X-ray diffraction evidence for the extensibility of actin and myosin filaments during muscle contraction.

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Journal:  Biophys J       Date:  1980-04       Impact factor: 4.033

Review 9.  The Life of Behavior.

Authors:  Alex Gomez-Marin; Asif A Ghazanfar
Journal:  Neuron       Date:  2019-10-09       Impact factor: 17.173

10.  Structural changes in the myosin filament and cross-bridges during active force development in single intact frog muscle fibres: stiffness and X-ray diffraction measurements.

Authors:  E Brunello; P Bianco; G Piazzesi; M Linari; M Reconditi; P Panine; T Narayanan; W I Helsby; M Irving; V Lombardi
Journal:  J Physiol       Date:  2006-09-21       Impact factor: 5.182

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  3 in total

1.  In vivo X-ray diffraction and simultaneous EMG reveal the time course of myofilament lattice dilation and filament stretch.

Authors:  Sage A Malingen; Anthony M Asencio; Julie A Cass; Weikang Ma; Thomas C Irving; Thomas L Daniel
Journal:  J Exp Biol       Date:  2020-09-03       Impact factor: 3.312

2.  A mechanism for sarcomere breathing: volume change and advective flow within the myofilament lattice.

Authors:  Julie A Cass; C David Williams; Thomas C Irving; Eric Lauga; Sage Malingen; Thomas L Daniel; Simon N Sponberg
Journal:  Biophys J       Date:  2021-08-10       Impact factor: 3.699

3.  Frequency-dependent signaling in cardiac myocytes.

Authors:  Payam Haftbaradaran Esfahani; Jan Westergren; Lennart Lindfors; Ralph Knöll
Journal:  Front Physiol       Date:  2022-09-02       Impact factor: 4.755

  3 in total

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